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Waffle House
Updated: April 1, 2021 12:00 PM
Covid-19 OSHA Complaint, Waffle House, 804 S Broad Street, CLINTON, SC, 29325, USA
Waffle House, 804 S Broad Street, CLINTON, SC, 29325, USA
April 1, 2021 12:00 PM
“A COVID-19 pandemic plan has not been developed and implemented for employees to include employee wellness checks, quarantining employees, informing employees of possible exposure to the virus, employee returning to work, social distancing, personal protective equipment, disinfecting/sanitizing, and... See Moreemployee training. An employee tested positive for COVID-19 and was not quarantined. Employees, who worked in direct contact with an employee who tested positive for COVID-19, were not informed for possible exposure to the virus. Employees are not wearing face covering; and there is no sanitation.
Source: Osha.gov | Receipt Date: 2020-12-30 See Less”
Helpful
Covid-19 OSHA Complaint, Waffle House #1632, 1100 Dallas Cherryville Hwy, DALLAS, NC, 28034, USA
Waffle House #1632, 1100 Dallas Cherryville Hwy, DALLAS, NC, 28034, USA
April 1, 2021 12:00 PM
“Employees could be exposed to the COVID-19 virus in the workplace, due to one or more employees having symptoms consistent with the infection, and the wearing of masks or wearing masks properly is not being enforced for employees or customers.
Source: Osha.gov | Receipt Date: 2021-02-19 See Less”
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Covid-19 OSHA Complaint, Waffle House #1707, 1444 East Main Street, LINCOLNTON, NC, 28092, USA
Waffle House #1707, 1444 East Main Street, LINCOLNTON, NC, 28092, USA
March 24, 2021 12:00 PM
“The employer is requiring employees to work next to an employee who has tested positive for COVID-19 and is allowed to stay at work.
Source: Osha.gov | Receipt Date: 2021-02-23 See Less”
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Covid-19 OSHA Complaint, Waffle House, Inc. - #1170, 101 Brook Lane, SPRING LAKE, NC, 28390, USA
Waffle House, Inc. - #1170, 101 Brook Lane, SPRING LAKE, NC, 28390, USA
March 10, 2021 12:00 PM
“On, but not limited to, January 22, 2021, employees were, or could have been, exposed to the COVID-19 virus in the workplace, due to an employee working that day while having symptoms consistent with those of a COVID-19 infection, and subsequently testing positive/being diagnosed with the illness.... See MoreSource: Osha.gov | Receipt Date: 2021-01-26 See Less”
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Covid-19 OSHA Complaint, Waffle House #1170, 101 Brook Lane, SPRING LAKE, NC, 28390, USA
Waffle House #1170, 101 Brook Lane, SPRING LAKE, NC, 28390, USA
March 10, 2021 12:00 PM
“One of the managers has tested positive for COVID-19 and is still working, exposing the entire staff. If the employees do not come into work, they will be terminated.
Source: Osha.gov | Receipt Date: 2021-01-25 See Less”
Helpful
Covid-19 OSHA Complaint, Waffle House, 408 Pratt Avenue Northeast, Huntsville, AL 35801, USA
Waffle House, 408 Pratt Avenue Northeast, Huntsville, AL 35801, USA
February 24, 2021 12:00 PM
“1. Employees who are experiencing COVID 19 symptoms are allowed to come to work. 2. Employees are not notified when coworkers receive a positive COVID-19 diagnosis. 3. The facility is not cleaned and sanitized in accordance with CDC guidelines to minimize employee exposure to COVID-19. 4. The employ... See Moreer does not enforce social distancing in accordance with CDC guidelines to minimize employee exposure to COVID-19.
Source: Osha.gov | Receipt Date: 2021-02-03 See Less”
Helpful
Covid-19 OSHA Complaint, Waffle House, 105 N Strand Pkwy, MYRTLE BEACH, SC, 29588, USA
Waffle House, 105 N Strand Pkwy, MYRTLE BEACH, SC, 29588, USA
February 2, 2021 12:00 PM
“The employer has not implemented good hygiene and infection control practices including social distancing, temperature checks, frequent and thorough hand washing, provide mask, gloves, maintain housekeeping like routine cleaning and disinfecting surfaces and equipment for the employees.
Source:... See MoreOsha.gov | Receipt Date: 2020-07-20 See Less”
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Covid-19 OSHA Complaint, Waffle House, Inc. - Waffle House #2171, 102 Pearces Road, ZEBULON, NC, 27597, USA
Waffle House, Inc. - Waffle House #2171, 102 Pearces Road, ZEBULON, NC, 27597, USA
January 13, 2021 12:00 PM
“There is concern that exposure to COVID-19 could occur, or could have occurred, at the restaurant, due to an employee being diagnosed with the infection; employees who had contact with the infected employee continuing to work; and the facility not being closed for cleaning.
Source: Osha.gov | Rec... See Moreeipt Date: 2020-08-25 See Less”
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Covid-19 OSHA Complaint, Waffle House, 2676 Columbia Hwy, AIKEN, SC, 29801, USA
Waffle House, 2676 Columbia Hwy, AIKEN, SC, 29801, USA
December 15, 2020 12:00 PM
“(1) Employees are not informed of other employees testing positive for Covid-19. The restaurant has not been properly sanitized. Mandatory mask wearing of the employees and periodic sanitizing of the stations is not been enforced.
Source: Osha.gov | Receipt Date: 2020-08-03 See Less”
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Covid-19 OSHA Complaint, Waffle House, Inc, 9009 Hwy 71, FORT SMITH, AR, 72908, USA
Waffle House, Inc, 9009 Hwy 71, FORT SMITH, AR, 72908, USA
December 2, 2020 12:00 PM
“Employer not enforcing good cleaning procedures for COVID-19, in areas where costumers have occupied within the establishment.
Alleged Hazards: 1, Employees Exposed: 23
Source: Osha.gov | Receipt Date: 2020-08-27 See Less”
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Recent Interesting Reports
April 6, 2021 10:19 PM
“Got the JnJ vaccine Monday morning 4/5/21 at Wegman’s Bridgewater. Other than my arm being a little sore I have no side effects at all. No head aches, no fevers, nothing! SIDE NOTE: I took a COVID test a few days before to confirm I was COVID free before getting vaccinated. I was on Claritin from th... See Moree night before because allergy season has officially started. I didn’t want the Moderna or Pfizer... not a fan of the lipid MRNA. - Stay Safe guys! See Less”
Helpful
2 people found this review 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”
Helpful
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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March 26, 2021 7:00 PM
“Company name: Namoo Enterprise LLC
Brand name: PremierZen
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and Tadalafil
FDA Recall date: March 26, 2021
Recall details: Little Ferry, NJ, Namoo Enterprise LLC is voluntarily recalling al... See Morel lots within expiry of PremierZen Black 5000 capsules to the consumer level. FDA analysis has found the product to contain undeclared sildenafil and tadalafil. Sildenafil and tadalafil, known as phosphodiesterase (PDE-5) inhibitors, are found in FDA approved products for the treatment of male erectile dysfunction.
The presence of sildenafil and tadalafil in PremierZen Black 5000 products makes them unapproved new drugs for which the safety and efficacy have not been established and therefore subject to recall. Risk Statement: Consumers with underlying medical issues who take PremierZen Black 5000 with undeclared sildenafil and tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates.
To date, Namoo Enterprise LLC has not received any reports of adverse events related to this recall. The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in card form with one capsule per card and is aware of at least one lot with an expiration date of December 2023. Each pack is black with gold, blue, white and red text. The capsule appears black and is enclosed within clear plastic on the package. The affected lots of PremierZen Black 5000 includes all lots. PremierZen Black 5000 was sold nationwide in the USA via the internet and fulfilled by ebay at www.ebay.com and also fulfilled by amazon at www.amazon.com.
On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms. Namoo Enterprise LLC is notifying its customers by this press announcement and by mailing recall letters. Consumers that have PremierZen Black 5000 should stop using and destroy them. Consumers with questions regarding this recall can contact Namoo Enterprise LLC by phone at 201-267-0539, Monday to Friday, 9 A.M. to 5 P.M. EST or email at namooenterprise@gmail.com from Monday to Friday.
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. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
April 12, 2021 11:56 PM
“I have had previous allergic reactions to nuts, but am happy to report I did not experience an allergic reaction as a result of having the Pfizer vaccine. I had it at about 4-5PM, and no immediate side effects. By the late evening my arm hurt and I didn’t want to lift it. By the next morning, the pa... See Morein had decreased, and by that evening it was completely gone. I have never had Covid before :^) See Less”
Helpful
1 person found this review helpful
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
March 31, 2021 10:00 AM
“Company name: Ummzy LLC
Brand name: Thumbs Up 7, Shogun, Krazy Night
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil, Tadalafil, Vardenafil
FDA Recall date: March 31, 2021
Recall details: Palisades Park, NJ, Ummzy LLC is voluntarily r... See Moreecalling all lots of Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night capsules to consumer level. FDA analysis has found the product to contain undeclared tadalafil sildenafil & Vardenafil. Tadalafil, Sildenafil & Vardenafil are ingredients known as phosphodiesterase (PD-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction. The presence of Tadalafil Sldenafil & Vardenafilin Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night capsules makes them unapproved new drugs for which the safety and efficacy have not been established and, therefore subject to recall.
Consumers with underlying medical issues who take Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night capsules with undeclared Tadalafil Sildenafil & Vardenafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening.
Consumers with diabetes, high blood pressure, or heart disease often take nitrates. To date, Ummzy LLChas not received any reports of adverse events related to this recall. This tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in blister foil sheets in a box containing 10 capsules. The affected lot numbers of Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night includes all lots. Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night was distributed nationwide in the USA via internet and fulfilled by amazon at www.amazon.com.
On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms. Ummzy LLC is notifying its customers by this press announcement and via e-mail of this recall.
Consumers that have Thumbs up 7 Red 70K, Shogun-X 15000mg, and Krazy Night, which is being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Ummzy LLC by phone at 201-416-9325 Monday to Friday from 9AM to 5PM or e-mail ysknabe75@gmail.com. For more information, please visit www.ummzyllc.com.
Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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”
Helpful
1 person found this review helpful
Pfizer vaccine 1st dose, CVS, Bagdad Road, Cedar Park, TX, USA
Symptoms: Soreness
CVS, Bagdad Road, Cedar Park, TX, USA
March 22, 2021 9:18 AM
“Arrived on time, just 4 people ahead of me, the line moved fast. I was out in about 20 minutes. They were well organized. It is now around 15 hours later and zero side effects, apart from some soreness at the injection site, similar to a flu shot. See Less”
Helpful
2 people found this review helpful
J&J one shot vaccine, Valencia, Santa Clarita, CA, USA
Symptoms: Nausea
Fever
Headache
Chills
Soreness
Valencia, Santa Clarita, CA, USA
April 5, 2021 7:15 PM
“Recieved my shot on 4/1/21 @ 2pm. By 10pm had a headache. Middle of the night low grade fever, chills, and nausea. Lasted 48 hours. Now 5 days out and still redess, soreness, and lump at injection site. See Less”
Helpful
1 person found this review helpful