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Tennessee, United States
Updated: April 7, 2021 12:00 PM
Covid-19 OSHA Complaint, Vitae Systems LLC, 4028 Papermill Drive Northwest, KNOXVILLE, TN, 37909, USA
Vitae Systems LLC, 4028 Papermill Drive Northwest, KNOXVILLE, TN, 37909, USA
April 7, 2021 12:00 PM
“The owner is not enforcing CDC guidelines to prevent the spread of COVID-19, such as mask wearing, availability of hand sanitizer, and cleaning protocol.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-25 See Less”
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Covid-19 OSHA Complaint, Clarksville Elite Gymnastics Center, LLC, 2231 Madison Street, CLARKSVILLE, TN, 37043, USA
Clarksville Elite Gymnastics Center, LLC, 2231 Madison Street, CLARKSVILLE, TN, 37043, USA
April 7, 2021 12:00 PM
“1. Employees are not being protected from potential exposure to COVID-19. 2. Employees do not wear masks or clean their hands. 3. High touch surfaces throughout the facility are not being sanitized. 4. Equipment is not being cleaned on the team side. 5. A thermometer is available for employee temper... See Moreature checks; however, it is not being used. 6. Employees diagnosed with COVID-19 are returning to work before finishing quarantine.
Source: Osha.gov | Receipt Date: 2021-02-04 See Less”
Helpful
Covid-19 OSHA Complaint, Hankook AtlasBX America Corp., 1325 International Blvd, CLARKSVILLE, TN, 37040, USA
Hankook AtlasBX America Corp., 1325 International Blvd, CLARKSVILLE, TN, 37040, USA
April 7, 2021 12:00 PM
“Respirators 1. Employees are asked to remove their respirator in high lead areas to speak with their coworkers. 2. Employees do not have plastic bags to store their respirators; during breaks respirators are hung on the wall and between shift they are stored in lockers. Respirators are not protected... See Morefrom contamination. Respirators are contaminated with lead. 3. Respirators are not assigned or identified, and other employees will use their coworker's respirator. 4. Employees are not provided with adequate training on respiratory protection. Hearing Protection 5. Employees are asked to remove their ear plugs in areas with high noise exposures to hear their co-workers. 6. Employees are required to reuse old, dirty earplugs for an entire week before getting a new pair., 7. The bell in the break room to inform that break time is over is too loud. Lead Contamination 8. Employees are not properly informed when they have elevated blood lead levels. Blood lead level results are posted in the break room with only the employee's birthdate to identify. 9. Employees have excessively high blood lead levels. 10. The entire plant is contaminated with lead. 11. Employees in the Mixing Department are not provided with D-Lead wipes to clean their workspace and equipment. 12. When mixing pasting/lead inside pasting machine dirt, dust, and lead flies into the operator's face. 13. Employees are allowed to bring their contaminated PPE into the break room. COVID-19 14. Employees are not protected from potential exposure to COVID-19. The time clocks, breakrooms, locker rooms, bathrooms, and shower rooms are not disinfected. 15. Recommendations regarding social distancing are not being followed, no social distancing in the break room. Employees are required to change clothes and shower at the same time preventing social distancing. 16. No temperature check on any shifts including days and nights for COVID-19. PPE 17. Employees are not provided with proper PPE. 18. Employees are not provided with training on how to wear protective clothing or PPE. 19. Employees are not provided with proper gloves to handle or work with liquid lead at the Holding Pot and Melting Pot. The gloves that are provided are too long and saggy making it difficult to grip or handle anything. The gloves have holes inside of them. 20. PPE is limited and shared in the WCRS Department. PPE is used by other departments so that it is not available when an operator needs PPE. 21. Operators throw solid lead into a melting pot or holding pot causing the liquid lead to splash. The splash of liquid lead does under the operator's face shield burning their face and head. 22. Not all employees have rubber boots in the pasting department; water gets into and on employee's shoes and clothing. 23. Employees are required to walk through the plant to access their PPE and respirator or mask. Employees are not protected from breathing in lead when walking to their PPE. Environmental Conditions 24. There is no hot water to take mandatory showers. 25. The bathrooms do not have towels to dry off after taking mandatory shower. 26. There are not paper towels in the break rooms to dry hands. 27. The employer doesn't provide rags or towels for employees to use to do their job, wipe up their areas, or wipe their sweat. 28. There are no nursing or 1st aid staff available to care for injured employees. No Jurisdiction 29. Employees personal belongings are being stolen out of their lockers. The employer is aware of this but does nothing to prevent it. 30. Employees are required to work on swing shifts resulting in the employees being exhausted. 31. Employees are encouraged to clock out before reporting work related injuries. Employees are not given access to proper workman's compensation physicians after a work injury. 32. There are no safety or human resources personnel on the night shift. 33. I feel I am over exposed to lead. I work in the WCRS and Pasting department. In the Robotic area
Source: Osha.gov | Receipt Date: 2021-01-12 See Less”
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Covid-19 OSHA Complaint, Plasma Biological Services, 3570 South Mendenhall Road, MEMPHIS, TN, 38119, USA
Plasma Biological Services, 3570 South Mendenhall Road, MEMPHIS, TN, 38119, USA
April 7, 2021 12:00 PM
“1. Employees are not following the safety rules. 2. Malfunctioning equipment (heat sealers) are catching fire and shocking the staff. 3. Employees are constantly running out of biohazard bins. 4. Mask are not strictly enforced by management for the donors. The agency does not have jurisdiction or st... See Moreandards to manage the following complaint items: 5. Donors out number the phlebotomists. There are supposed to be only 6 donors per person but we are working 12 donors per person and this poses as a safety hazard.
Source: Osha.gov | Receipt Date: 2021-03-02 See Less”
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Covid-19 OSHA Complaint, Marq Labs, 291 Edgewood Street, ALEXANDRIA, TN, 37012, USA
Marq Labs, 291 Edgewood Street, ALEXANDRIA, TN, 37012, USA
April 7, 2021 12:00 PM
“1. Aisles are obstructed by pallets and boxes 2. Adequate protective measures for protection from Covid19 virus not being taken
Alleged Hazards: 2, Employees Exposed: 50
Source: Osha.gov | Receipt Date: 2021-02-19 See Less”
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Covid-19 OSHA Complaint, Salga Plastics Inc., 241 ABC Boulevard, GALLATIN, TN, 37066, USA
Salga Plastics Inc., 241 ABC Boulevard, GALLATIN, TN, 37066, USA
April 7, 2021 12:00 PM
“1. Forklift operators do not wear their seatbelts, some are broken and cannot be buckled 2. Water and oil leaking from the molding machines is always on floor 3. Guards on the Tester Clamps do not work 4. Cranes moving loads above employees' heads 5. Hard hats, safety eyewear, and safety footwear ar... See Moree not used 6. Safety lights are not working on some forklifts 7. Not enough toilets for the number of workers 8. The company is not following Covid-19 guidelines.
Alleged Hazards: 8, Employees Exposed: 150
Source: Osha.gov | Receipt Date: 2021-02-12 See Less”
Helpful
April 6, 2021 5:55 PM
“I got the Pfizer shot yesterday at Walgreens. I will return in 3 weeks to get the second dose. I just had a slight headache and a bit of soreness in the arm. That being said I am sure it is better than get COVID. See Less”
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Covid-19 OSHA Complaint, Top Jump LLC, 3735 Parkway, PIGEON FORGE, TN, 37876, USA
Top Jump LLC, 3735 Parkway, PIGEON FORGE, TN, 37876, USA
April 1, 2021 12:00 PM
“Employees not wearing masks(e.g. in the jump area). Employeee's not sanitizing common surfaces and equipment.
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-02-22 See Less”
Helpful
Covid-19 OSHA Complaint, Country Corner Restaurant, 2012 Snapps Ferry Road, GREENEVILLE, TN, 37745, USA
Country Corner Restaurant, 2012 Snapps Ferry Road, GREENEVILLE, TN, 37745, USA
April 1, 2021 12:00 PM
“Employees are not wearing masks.
Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-02-22 See Less”
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Covid-19 OSHA Complaint, City of Memphis Credit Union, 2608 Avery Avenue, MEMPHIS, TN, 38112, USA
City of Memphis Credit Union, 2608 Avery Avenue, MEMPHIS, TN, 38112, USA
April 1, 2021 12:00 PM
“Employer is not taking steps to protect employees from exposure to SARS-COV-2(COVID-19).
Source: Osha.gov | Receipt Date: 2021-02-08 See Less”
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Recent Interesting Reports
March 27, 2021 11:00 PM
“Company name: Midwestern Pet Foods
Brand name: Multiple brands
Product recalled: Dog and Cat Food
Reason of the recall: Potential Salmonella Contamination
FDA Recall date: March 27, 2021
Recall details: Midwestern Pet Foods, Evansville, Indiana is issuing a voluntary recall of specific expirati... See Moreon dates of certain dog and cat food brands including CanineX, Earthborn Holistic, Venture, Unrefined, Sportmix Wholesomes, Pro Pac, Pro Pac Ultimates, Sportstrail, Sportmix and Meridian brands produced at its Monmouth, Illinois Production Facility because they have the potential to be contaminated with Salmonella. A full list of recalled products may be found at the end of this announcement. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.
Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.
Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian. No human or pet illnesses have been reported to date.
Products were distributed to retail stores nationwide and to online retailers. Lot code information may be found on the back of the bags with the following format: “EXP AUG/02/22/M1/L# See Example Image Below This recall covers only certain products manufactured at Midwestern Pet Foods Monmouth, Illinois facility. The unique Monmouth Facility identifier is located in the date code as an “M”. The recall was as the result of a routine sampling program by the company which revealed that the finished products may contain the bacteria.
Retailers and distributors should immediately pull recalled lots from their inventory and shelves. Do not sell or donate the recalled products. Retailers are encouraged to contact consumers that have purchased the recalled products if the means to do so exists. Do not feed the recalled products to pets or any other animals. Destroy the food in a way that children, pets and wildlife cannot access them. Wash and sanitize pet food bowls, cups and storage containers.
Always ensure you wash and sanitize your hands after handling recalled food or any utensils that come in contact with recalled food. Contact Midwestern Pet Foods Consumer Affairs at info@midwesternpetfoods.com or 800-474-4163, ext 455 from 8 AM to 5 PM Central Time, Monday through Friday for additional information. This voluntary recall is being conducted in cooperation with the US Food and Drug Administration. All other Midwestern Pet Foods products are unaffected by this recall.
Check the full recall details on fda.gov
Source: FDA See Less”
Doctor Visit: Yes
Diagnosis: Salmonella
Helpful
April 12, 2021 1:00 PM
“Company name: J. M. Smucker Co.
Brand name: Meow Mix®
Product recalled: Meow Mix® Original Choice Dry Cat Food
Reason of the recall: Potential Salmonella Contamination
FDA Recall date: April 12, 2021
Recall details: Orrville, OH – The J. M. Smucker Co. today announced a limited, voluntary recal... See Morel of two lots of Meow Mix® Original Choice Dry Cat Food (30LB bag) due to potential salmonella contamination. The Company has received no reports of pet illness or adverse reaction and has issued this recall out of an abundance of caution.
The impacted products were sold at select Walmart stores in IL, MO, NE, NM, OK, UT, WI, and WY. No other Meow Mix® products are impacted by this recall. If pet parents have products matching the following description in their possession, they should stop feeding it to their cats and dispose of it immediately. This information can be found on the bottom and back of each bag.
- Meow Mix® Original Choice Dry Cat Food (30 LB Bag). Retail UPC Code: 2927452099. Lot Code: 1081804. Best If Used By Date: 9/14/2022
- Meow Mix® Original Choice Dry Cat Food (30 LB Bag). Retail UPC Code: 2927452099. Lot Code: 1082804. Best If Used By Date: 9/15/2022
Check the full recall details on fda.gov
Source: FDA See Less”
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April 13, 2021 11:07 PM
“I just received my first dose today. The shot was completely painless. I did not have any soreness in my arm until a few hours later. No side effects so far. I have been feeling good after the shot. My next one is in 21 days. See Less”
Helpful
After first Moderna shot, Sebastopol, CA, USA
Symptoms: Other
Body Ache
Soreness
Sebastopol, CA, USA
March 26, 2021 5:51 PM
“Sore arm first night, much like a flu shot. In subsequent days had achy lymph nodes in armpit, neck and upper chest. No big deal, just rather odd. 9 days after shot I woke with first Atrial fib in almost 6 weeks (had second Cardiac ablation last summer that we hoped would "fix" it). I had Afib episo... See Moredes next two nights, decreasing in intensity, but certainly requiring meds and monitoring. Since been diagnosed with Afib bit over 2 years ago had never had it multiple days in a row before.
Since then, every days it's less problematic. Now just an hour of feeling a tad funky in the afternoons.Asked my cardiologist if he'd had other patients with similar reactions and he said "yes", but mostly after second vaccination. Seems as if the inflammation that's triggered by vaccine as body responds and creates antibodies to virus, triggers "twitchy" susceptible heart into freaking out (my language, not his!) Makes me rather dread how I"m going to feel next week after second shot, But will certainly not deter me to get fully covered. See Less”
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1 person found this review helpful
March 24, 2021 4:00 PM
“Company name: Alembic Pharmaceuticals, Inc.
Brand name: Alembic
Product recalled: Telmisartan Tablets, USP, 20 mg
Reason of the recall: Incorrect Product Strength on Label
FDA Recall date: March 24, 2021
Recall details: Bridgewater, NJ, Alembic Pharmaceuticals, Inc is voluntarily recalling on... See Moree lot of Telmisartan Tablets, USP, 20 mg, packaged in 30-count bottles, Lot No. 1905005661 to the consumer level. The product is being recalled due to a market complaint received which stated that one bottle labelled as 30-count Telmisartan Tablets, USP, 20 mg incorrectly contained 30 tablets of Telmisartan Tablets, USP, 40mg.
Risk Statement: Patients who could be on a doubled dose of telmisartan for a prolonged period of time, could experience low blood pressure, worsening of kidney function, or an elevation of potassium which can be life-threatening. To date, Alembic Pharmaceuticals Limited has not received any reports of adverse events related to this recall. The product is used for the treatment of hypertension i.e. to lower blood pressure and is packaged in a bottle of 30 tablets having NDC Number 62332-087-30.
The affected lot of Telmisartan Tablets, USP, 20 mg is the lot number 1905005661 and the lot expires in March 2022. The wrong product can be identified by checking the shape and embossing details on the tablets i.e. Telmisartan Tablets, USP, 20 mg bottles may incorrectly contain oval shaped White to off-white tablets debossed with L203 on one side instead of correct product i.e. round shaped White to off-white tablets debossed with L 202 on one side. Telmisartan Tablets, USP, 20mg, Lot No. 1905005661 was distributed Nationwide in the USA to wholesalers, retailers, and pharmacies.
Alembic Pharmaceuticals Limited is notifying its distributors and retailers through letter and is arranging for return of the recalled lot. Consumers that may have Telmisartan Tablets, USP, 20 mg which is being recalled should not discontinue use until speaking with their pharmacist or healthcare professional for a replacement before returning to place of purchase. Consumers with questions regarding this recall can contact Alembic Pharmaceuticals Inc by phone at +1 908-552-5839 (9:00 am – 5:00 pm, EDT, Monday through Friday) or email address david.cobb@alembicusa.com.
Check the full recall details on fda.gov
Source: FDA See Less”
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1 person found this review helpful
March 25, 2021 11:00 AM
“Company name: Zydus Pharmaceuticals Inc.
Brand name: Zydus Pharmaceuticals
Product recalled: Acyclovir Sodium Injection, 50 mg/mL, 10 mL and 20 mL vials
Reason of the recall: Due to Crystalization
FDA Recall date: March 25, 2021
Recall details: Pennington, NJ, Zydus Pharmaceuticals (USA) Inc. i... See Mores voluntarily recalling four lots of Acyclovir Sodium Injection, 50 mg/mL, 10 mL and 20 mL vials, to the Hospital/User level after receiving several complaints of crystallization in vials.
Administration of crystalized Acyclovir Sodium Injection, 50 mg/mL has a potential of life-threatening adverse consequences including injection site inflammation of a vein and local reactions, damage and/or obstruction of blood vessels, which could induce clots, particularly in the lungs, the passage of the particulate matter into the bloodstream may lead to clots resulting in stroke, heart attack, decreased liver or kidney function or death of tissues or cells.
To date, Zydus Pharmaceuticals (USA) Inc. has not received any reports of adverse events related to this product recall. Acyclovir Sodium Injection, 50 mg/mL is indicated for the treatment of herpes simplex infections in immunocompromised patients, severe initial clinical episodes of herpes genitalis in immuno-competent patients, herpes simplex encephalitis, neonatal herpes simplex virus infection and varicella-zoster (shingles) infections in immunocompromised patients.
The product is packaged in single-dose glass vials and was distributed nationwide in the USA to Cardinal Health, Amerisourcebergen Drug Corporation and Morris & Dickson Company LLC. The affected Acyclovir Sodium Injection, 50 mg/mL lots include the following lot numbers and expiration dates:
- Acyclovir Sodium Injection, 50 mg/mL, 20 mL. Carton NDC Number: 68382-049-10. Vial NDC Number: 68382-049-01. Lot Number: L000155. Expiry Date: Dec 2021. Pack Size: 10x20 mL, Single-Dose Vial pack.
- Acyclovir Sodium Injection, 50 mg/mL, 20 mL. Carton NDC Number: 68382-049-10. Vial NDC Number: 68382-049-01. Lot Number: L000156. Expiry Date: Jan 2022. Pack Size: 10x20 mL, Single-Dose Vial pack.
- Acyclovir Sodium Injection 50 mg/mL, 10 mL. Carton NDC Number: 68382-048-10. Vial NDC Number: 68382-048-01. Lot Number: L000126. Expiry Date: Dec 2021. Pack Size: 10x10 mL, Single-Dose Vial pack.
- Acyclovir Sodium Injection 50 mg/mL, 10 mL. Carton NDC Number: 68382-048-10. Vial NDC Number: 68382-048-01. Lot Number: L000127. Expiry Date: Dec 2021. Pack Size: 10x10 mL, Single-Dose Vial pack.
Zydus Pharmaceuticals (USA) Inc. has notified its distributors and customers by email and FedEx overnight courier service and is arranging for the return of all recalled Acyclovir Sodium Injection, 50 mg/mL lots. Hospitals that have the product which is being recalled should stop using it immediately and call our recall coordinating center at 1-855-671-5023 [Call: 1-855-671-5023] Monday – Friday (excluding holidays), 9:00 am to 5:00 pm EST.
Consumers with questions regarding this recall can contact Zydus Pharmaceuticals (USA) Inc. by phone: 1-877-993-8779 [Call: 1-877-993-8779] or by email: medicalaffairs@zydususa.com Monday – Friday (excluding holidays), 9:00 am to 5:00 pm EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Check the full recall details on fda.gov
Source: FDA See Less”
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1 person found this review helpful
March 16, 2021 5:00 PM
“Company name: Bravo Packing, Inc.
Brand name: Bravo Packing, Inc.
Product recalled: Pet food: Performance Dog, beef, green tripe, and bone
Reason of the recall: Due to Potential Salmonella and Listeria monocytogenes
FDA Recall date: March 16, 2021
Recall details: Bravo Packing, Inc. of Carneys... See MorePoint, NJ is expanding the previously announced voluntary recall of two pet food products to now include all pet food and bones in all package sizes. During an FDA inspection, samples collected tested positive for Salmonella and Listeria monocytogenes and resulted in a recall due to the potential health risks to humans and pets. Bravo Packing, Inc. is expanding the recall due to potential cross contamination.
No human or animal illnesses related to the identified products have been reported to date. Bravo Packing Inc. generally works with distributors that fill orders to retail stores and to consumers directly nationwide. Consumers with any of the affected products should handle them with caution, discard products in a secure container, and wash hands and surfaces properly. Consumers with questions should contact Bravo Packing, Inc. at 856-299-1044 (Monday – Friday, 9:00 AM-2:00 PM, EST). Recalled Products:
- “Performance Dog” (chub) frozen raw dog food (2 lbs.)
- “Performance Dog” (chub) frozen raw dog food (5 lbs.)
- “Green Tripe” (chub - ground bovine stomach) frozen raw dog food (2 lbs.)
- “Green Tripe” (chub - ground bovine stomach) frozen raw dog food (5 lbs.)
- “Beef” (chub - ground) frozen raw dog food (2 lbs.)
- “Beef” (chub - ground)frozen raw dog food (5 lbs.)
- “Performance Dog” (patties) frozen raw dog food (unknown)
- “Tripe” (patties ¼ lbs.) frozen raw dog food (unknown)
- Bones (smoked) 14 varieties (unknown)
Salmonella can cause illness in pets eating the products, as well as people who handle contaminated pet food products, especially if they have not thoroughly washed their hands after having contact with the products, infected pets, or any surfaces exposed to these products. People infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping, and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis (an infection of the heart muscle), arthritis, muscle pain, eye irritation, and urinary tract symptoms. People who have these symptoms after having contact with the products identified in this recall or with a pet that has eaten these products should contact their healthcare providers.
A pet with a Salmonella infection may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have decreased appetite, fever, and abdominal pain. If your pet has consumed the recalled products and has these symptoms, please contact your veterinarian. Pets exposed to contaminated food can be infected without showing symptoms. Infected pets, including those without symptoms, can also shed Salmonella through their feces and saliva, spreading pathogens into the home environment and to humans and other animals nearby.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, Listeria monocytogenes infection can cause miscarriages and stillbirths among pregnant women.
Check the full recall details on fda.gov
Source: FDA See Less”
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1 person found this review helpful
March 17, 2021 11:00 AM
“Company name: PNHC, LLC d/b/a Heal the World
Brand name: Heal the World
Product recalled: Hand Sanitizer
Reason of the recall: Because they resemble water bottles; risk of ingestion
FDA Recall date: March 17, 2021
Recall details: Raleigh, North Carolina, PNHC, LLC, d/b/a Heal the World, is vol... See Moreuntarily recalling all lots of Heal the World hand sanitizer packaged in 9.6 fl. oz containers to the consumer level. The products are being recalled because they resemble 9.6ounce water bottles. The recall does not affect any other Hand Sanitizer products from PNHC, LLC and/or Heal the World.
- Heal the World Hand Sanitizer (9.6 FL. OZ (285 mL)). NDC: 73333-285-01. Lot Nos. SAA21, SAA24, SAA27, SAA22, SAA23, SAA29, SAA26, SAA28, SAA25, SAA32, SAA55, SAA56, SAA44, SAA60.
To date, PNHC, LLC, d/b/a Heal the World has received no reports of adverse reactions and no complaints have been received. Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute.
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in 9.6 ounce plastic bottles. The product can be identified by the bottle’s label pictured below. Product was distributed to selected retailers in the United States.
PNHC, LLC has provided notification to its distributors and retailers. Distributors and retailers that have product which is being recalled should stop distribution. While the product is not available for purchase and has not been available for several months, if a consumer has product which is being recalled he or she is advised to contact the entity who sold the product to consumer for return.
Consumers with questions regarding this recall can contact PNHC, LLC at 813-434-0741 from 9:00 am- 5:00 pm EST, Monday through Friday. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.
Check the full recall details on fda.gov
Source: FDA See Less”
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Johnson&Johnson vaccine, Kansas City, KS, USA
Kansas City, KS, USA
April 9, 2021 3:15 PM
“I got the j&j vac at 1:00pm its been 1 hour so far only a slight tingling on vaccination spot other than that nothing big hoping for the best See Less”
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1 person found this review helpful
March 25, 2021 9:01 AM
“Company name: Sanit Technologies LLC d/b/a Durisan
Brand name: Durisan
Product recalled: Antimicrobial Hand Sanitizer
Reason of the recall: Due to microbial contamination
FDA Recall date: March 24, 2021
Recall details: Sanit Technologies LLC d/b/a Durisan announces a voluntary recall of the lot... See Mores listed in the table below of Durisan Antimicrobial Hand Sanitizer, Non-Alcohol products in various sizes listed. The products are being recalled due to microbial contamination. Specifically, out of specification results for bacterial count for Burkholderia cepacia complex and Ralstonia pickettii. The issue was discovered during a routine audit focused on production scale-up during the height of the pandemic.
Check the link below for the full list of Durisan Antimicrobial Solutions Hand Sanitizer Sizes and Lot Numbers. To date, no reports of adverse reactions or customer complaints have been reported related to this recall.
The product was packaged in sizes ranging from 18mL credit cards, to bottles sized in 118, 236, 300 and 550 mL and 1000mL wall mounted dispenser refills. Pictures are available in the attached related file.
Use of a hand sanitizer contaminated with Burkholderia cepacia complex and Ralstonia pickettii, can range from no reaction to serious infections in a person with a hand wound or scrapes because the bacteria could enter the bloodstream, especially in patients with compromised immune systems. Health care professionals who use this contaminated hand sanitizer and tend to an at-risk patient, such as one with cystic fibrosis, could lead to adverse events ranging from a localized infection to lung or bloodstream infections, which could require patient hospitalization.
The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available. The product can be identified by examples of the product labels below. The product was manufactured from Feb. 1, 2020 until June 30, 2020, and distributed to selected retailers nationwide in the United States.
Durisan has provided written notification to its distributors and retailers and is alerting customers via this voluntary recall. Consumers that have the product which is being recalled are advised to destroy it immediately.
Consumers with questions regarding this recall can contact Durisan at 941-351-9114 [Call: 941-351-9114] , 8:30 am - 4:30 pm Eastern time, Monday through Friday or by e-mail at customerservice@durisan.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
Check the full recall details on fda.gov
Source: FDA See Less”
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1 person found this review helpful