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Burger King
Updated: April 7, 2021 12:00 PM
Covid-19 OSHA Complaint, Burger King, 28991 W Gonzaga Rd, SANTA NELLA, CA, 95322, USA
Burger King, 28991 W Gonzaga Rd, SANTA NELLA, CA, 95322, USA
April 7, 2021 12:00 PM
“1. 3205: Employer is not following state guidelines regarding COVID-19 protocol. Employees are not wearing masks, and there is no signage on the door to wear masks.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-03-03 See Less”
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Covid-19 OSHA Complaint, Burger King, 4200 International Boulevard, OAKLAND, CA, 94601, USA
Burger King, 4200 International Boulevard, OAKLAND, CA, 94601, USA
April 1, 2021 12:00 PM
“1. The employer is failing to send home employees who report feeling ill or showing signs and symptoms of COVID-19. Employees in November and December reported feeling ill and were asked to take medicine and stay at work. T8 CCR 3205(c)(4) 2. The employer is failing to notify and/or quarantine close... See Morecontacts to employees who were suspected of having COVID-19. Employees in November and December all spent time at home away from work and no employees were notified or quarantined for close contact exposure. T8 CCR 3205(c)(3)(b)(3)(a) 3. The employer is failing to screen employees for signs and symptoms when they come to work. Management does not ask questions if employees are having signs or symptoms. T8 CCR 3205(c)(2)(B) 4. The employer is failing to train employees in the topics of COVID-19, such as social distancing and cleaning of high touch areas. T8 CCR 3205(c)(5) 5. The employer is failing to ensure that all practical solutions are in place to maintain social distancing. The chicken and fry station are in close proximity and sometimes is close to the drive thru station. Management has not adjusted the work schedule to allow for more social distancing. T8 CCR 3205(c)(6)(A) 6. The employer failed to implement a written plan for COVID-19 with policy and procedures. There is not a written plan in place to outline how often areas are cleaned, how often employees are to wash their hands, and how to maintain as much social distancing as possible. T8 CCR 3205(c) 7. The employer is failing to enforce that employees wash their hands frequently while in the workplace. T8 CCR 3205(c)(8)(D) 8. The employer is failing to ensure that high touch areas are cleaned frequently. T8 CCR 3205(c)(8)(C)
Alleged Hazards: 8, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-26 See Less”
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Covid-19 OSHA Complaint, Burger King Store #9833, 6411 Blue Star Hwy, SAUGATUCK, MI, 49453, USA
Burger King Store #9833, 6411 Blue Star Hwy, SAUGATUCK, MI, 49453, USA
April 1, 2021 12:00 PM
“'- Failure to follow proper covid-19 procedures. - Employees do not wear gloves when putting hands near or in food, such as fries, nuggets, and sides. - Employees do not wash their hands regularly, or not at all. - Sanitation of the lobby, kitchen, and service area is not done. - When out of the cus... See Moretomer's sight, employees do not wear masks, and the night crew does not wear them in general, especially in the kitchen. - The employee operating the window handles customers' food and money without wearing protection or using different methods for the protection of the customer. - When checking and monitoring for covid-19, the managers are negligent when making sure employees are safe. Managers falsify temperature taking and fail to take symptoms of the virus seriously. - An employee had several symptoms and was very sick but proceeded to work the entire day because of being understaffed. - The employer fails to follow health procedures such as serving food that is old and stale and fails to keep kitchen-cleaning a priority. - The building and kitchen only get mopped once a day, creating unsafe floor surfaces from grease to slippery food. - Employees also do drugs and smoke inside of the restaurant, and then breathe all over and do not wash their hands.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-09-14 See Less”
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Covid-19 OSHA Complaint, Burger King, 2752 HWY 50 South, GRAND JUNCTION, CO, 81503, USA
Burger King, 2752 HWY 50 South, GRAND JUNCTION, CO, 81503, USA
March 24, 2021 12:00 PM
“1. It has been reported that employees are not wearing their face masks correctly. It has been reported that employees are wearing their face masks below their noses. This condition exposes employees to COVID-19. Contrary to Section 5(a)(1) of the OSH Act.
Alleged Hazards: 1, Employees Exposed: 10... See MoreSource: Osha.gov | Receipt Date: 2020-11-09 See Less”
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Covid-19 OSHA Complaint, Burger King, 2925 Bridge Road, SUFFOLK, VA, 23435, USA
Burger King, 2925 Bridge Road, SUFFOLK, VA, 23435, USA
March 24, 2021 12:00 PM
“Located at Burger King where an employee has tested positive, the employer is not implementing precautions to protect employees from contracting and spreading the Coronavirus (COVID-19) in the workplace in that: 1. Employees are not informed when they have been in contact with a COVID-19 positive em... See Moreployee 2. Cleaning activities are not conducted in areas were COVID-19 positive employees have worked prior to allowing other employee access to those areas 3. Burger King do not have a COVID-19 Preparedness and Response Plan 4. COVID-19 training is not given to employees.
Source: Osha.gov | Receipt Date: 2021-01-19 See Less”
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Covid-19 OSHA Complaint, Burger King, 4883 Kentucky Ave, INDIANAPOLIS, IN, 46221, USA
Burger King, 4883 Kentucky Ave, INDIANAPOLIS, IN, 46221, USA
March 17, 2021 12:00 PM
“Employees who have been expsoed to COVID-19 are continuing to come into work. No sanitization or cleaning has been done in the facility.
Source: Osha.gov | Receipt Date: 2020-12-14 See Less”
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Covid-19 OSHA Complaint, Burger King, 2 Continental Boulevard, MERRIMACK, NH, 03054, USA
Burger King, 2 Continental Boulevard, MERRIMACK, NH, 03054, USA
March 17, 2021 12:00 PM
“1. The employer is not following OSHA and CDC guidelines for protecting employees during the covid-19 pandemic including, but not limited too, allowing Covid-19 positive employees to report to work and allow them to work knowing that they are ill or have tested positive for Covid-19
Alleged Hazards... See More: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-02-10 See Less”
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Covid-19 OSHA Complaint, Burger King, 737 DW Highway, MANCHESTER, NH, 03104, USA
Burger King, 737 DW Highway, MANCHESTER, NH, 03104, USA
March 17, 2021 12:00 PM
“1. The employer is not following OSHA and CDC guidelines for protecting employees during the covid-19 pandemic, including: - The employer is not doing contract tracing when employees test positive for Covid-19 after reporting to work. - The employer is not following quarantine guidelines for employe... See Morees who are primary contacts for Covid-19.
Alleged Hazards: 2, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2021-01-25 See Less”
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Covid-19 OSHA Complaint, Burger King, 2757 Castro Valley Boulevard, CASTRO VALLEY, CA, 94546, USA
Burger King, 2757 Castro Valley Boulevard, CASTRO VALLEY, CA, 94546, USA
February 24, 2021 12:00 PM
“1. The employer failed to notify employees exposed to COVID-19 and exclude them from the workplace. T8 CCR 3205(c)(1)(D) & (c)(10) 2. The employer failed to ensure that face coverings are worn by customers in the drive-thru. T8 CCR 3205(c)(7)(A) 3. The employer failed to provide employees with train... See Moreing in regards to COVID-19 hazards and safe work practices. T8 CCR 3205(c)(5) 4. The employer failed to frequently clean and decontaminate commonly touched surfaces. T8 CCR 3205(c)(8)(C) 5. The employer failed to maintain employees' earnings and benefits when they are excluded from the workplace due to COVID-19. T8 CCR 3205(c)(10)(C)
Alleged Hazards: 5, Employees Exposed: 3
Source: Osha.gov | Receipt Date: 2020-12-24 See Less”
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Covid-19 OSHA Complaint, Burger King, 1080 South University Avenue, PROVO, UT, 84601, USA
Burger King, 1080 South University Avenue, PROVO, UT, 84601, USA
February 24, 2021 12:00 PM
“Employees not wearing masks as required for COVID-19
Alleged Hazards: 1, Employees Exposed: 16
Source: Osha.gov | Receipt Date: 2021-02-08 See Less”
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Recent Interesting Reports
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 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 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
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”
Helpful
1 person found this review helpful
Pfizer First Dose Vaccine, Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA
Symptoms: Headache
Fatigue
Soreness
Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA
April 2, 2021 7:33 PM
“The vaccine process went relatively smooth. Waited the recommended 15 minutes for any allergic reactions. Had none. My side effects have been mild. Headache, run down feeling, head fogginess, sore arm from where the vaccine was injected, alittle fatigued, and have noticed my heart rate being alittle... See Moretoo high for comfort. See Less”
Helpful
1 person found this review helpful
Blackcass.com. Never received order, Caledonia, NY, USA
Caledonia, NY, USA
April 5, 2021 4:16 PM
“I ordered a Stihl battery operated hand held saw off the internet for $37.00 and got a chain with 2 cloth handles. I would like my saw or money back. 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”
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April 7, 2021 11:00 AM
“Company name: Yolo Studio
Brand name: PremierZEN Extreme 3000, PremierZEN Plus 5000, & Triple SupremeZEN Plus 3500
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Tadalafil
FDA Recall date: April 06, 2021
Recall details: Cliffside Park, NJ, Yol... See Moreo Studio is voluntarily recalling all lots of PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 to the consumer level. FDA analysis has found the product to contain undeclared tadalafil. Tadalafil is ingredient known as a phosphodiesterase (PDE-5) inhibitor found in FDA approved products for the treatment of male erectile dysfunction.
The presence of tadalafil in PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 makes these 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 PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 with undeclared 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, Yolo Studio has not received any reports of adverse events related to this recall. These tainted products are marketed as dietary supplements for male sexual enhancement and are packaged in cardboard blisters containing one pill per card.
The affected lot numbers of PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 include all lots. PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 were distributed via internet and fulfilled by amazon at www.amazon.com nationwide in the USA. 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. Yolo Studio is notifying its customers by this press announcement and via e-mail of this recall. Consumers that have PremierZEN Extreme 3000, PremierZEN Black 5000, & Triple SupremeZEN Plus 3500 which are being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Yolo Studio by phone at (201) 233-3521 Monday through Friday from 9am to 5pm eastern time zone or e-mail yolostudiodamazon@gmail.com.
Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to taking or using these drug products. 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”
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I am reporting Pfizer vaccine, Lecompte, LA 71346, USA
Symptoms: Other
Headache
Lecompte, LA 71346, USA
March 22, 2021 7:48 PM
“In February I received my 1st dose of Pfizer vaccine and I did get a headache.. yet it was the second dose on March 3 that made me go to the doctor and found that that vaccine has cause me to have high high blood pressure! My numbers doubled and I have not recovered. Now on high blood pressure me... See Moreds. The doctor says I have fluid built up around my heart and palpitations that are driving me to unhappy days.
Letting you know. . See Less”
Helpful
5 people found this review helpful
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
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