Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case! Your contact information is not shown on the website.
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Use camera
Select from library
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!
IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)
Visit our learn pages for more helpful information or, email us: support@safelyhq.com
Goodbye! and best wishes in your recovery
Report by
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

If your report is poison related call 1-800-222-1222 for a free consultation with a live medical poisoning expert

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Pfizer Covid-19 vaccine, Columbus, OH, USA

April 7, 2021 9:02 PM

Columbus, Ohio, United States

Symptoms: Soreness

I had the first shot of the Pfizer vaccine on 2/17/21 and the second shot on 3/10/21. I had no side effects except slight injection site pain for about 24 hours after each shot.

Reported By SafelyHQ.com User

Related Reports

April 19, 2021 7:57 PM

“Only symptom I had was a sore arm the next day. The third day I feel just fine. See Less
Reported By SafelyHQ.com User

1st and 2nd Pfizer Shot, Hollywood, FL, USA

Symptoms: Fever Headache Joint Pain
Hollywood, FL, USA

April 19, 2021 9:13 PM

“1st shot went relatively well. Had only minor tightness of throat for few minutes, felt light headed, and then felt feverish for a few days. Had join pain for a few days, but it got better later. Felt much better overall in a few days, better than before the shot. The second shot went well also, no... See Moretightness in the throat, no light headed, only soreness of arm for about two days. However, after one week, getting headaches/ mild migranes that don't go away and I don't really suffer from these. Had no major changes in routine or sleep habit to attribute to it. Headaches got worse after one week being vaccinated. Also, had a few episodes of weird symptoms I had never felt before- like if the heart skipped a beat... If it will continue, I will address this with my doctor. At this point, sharing, so that if anyone else has similar symptoms, we can bring it to the attention it needs. Overall, feel better than before getting the shot. I suspect I might have had long haul symptoms from possible Covid in March 2020- no tests were available to me to confirm the positivity then, but had many weird illnesses that are better now. The irregular heart beat/shortness of breath on occasion (only one to two seconds) concerns me a little. At this point, still happy I got the shot as I'm in the high risk category from complications and could not risk not getting vaccinated. See Less
Reported By SafelyHQ.com User

4 days after 1st Moderna vacx, Boston, MA, USA

Symptoms: Fever Cramps Headache Chills Joint Pain Muscle Pain
Boston, MA, USA

April 19, 2021 9:42 PM

“Moderna vacx or tasting (approx tablespoon perhaps-spoiled chicken salad) After this questionnaire I think my symtoms may have been a delay result of the vaccine.
Joint and muscle aches ALL over, chills, headache,abdominal cramp-like pain, temp max'd at 101.6° ... Took two caps Tylenol at 24 hrs.... See MoreSlept thru night awoke next morning (.. All symptoms completely gone! See Less
Reported By SafelyHQ.com User
SMB Screener

Covid-19 OSHA Complaint, Grandad's Pizza, 1254 West 3rd Avenue, COLUMBUS, OH, 43212, USA

Grandad's Pizza, 1254 West 3rd Avenue, COLUMBUS, OH, 43212, USA

April 7, 2021 12:00 PM

“The employer has not taken the appropriate steps to protect employees from SARS-C0V-2, the virus that causes COVID-19. It was alleged that the employer does not instruct workers who are infected or potentially infected to stay home and isolate or quarantine, does not isolate workers who show symptom... See Mores at work and employees do not wear masks properly.

Alleged Hazards: 1, Employees Exposed: 8
Source: Osha.gov | Receipt Date: 2021-03-15
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, U.S. Postal Service, 2323 City Gate Drive, COLUMBUS, OH, 43218, USA

U.S. Postal Service, 2323 City Gate Drive, COLUMBUS, OH, 43218, USA

April 7, 2021 12:00 PM

“The employer has not taken the appropriate steps to protect employees from SARS-C0V-2, the virus that causes COVID-19. The employer does not instruct workers who are infected or potentially infected to stay home and isolate or quarantine, does not isolate workers who show symptoms at work, and does... See Morenot thoroughly clean and disinfect immediate work areas and equipment used by potentially infected personnel.

Alleged Hazards: 1, Employees Exposed: 200
Source: Osha.gov | Receipt Date: 2021-03-12
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Pastimes Pub & Grill Crosswoods, 121 East Campus View Boulevard, COLUMBUS, OH, 43235, USA

Pastimes Pub & Grill Crosswoods, 121 East Campus View Boulevard, COLUMBUS, OH, 43235, USA

April 1, 2021 12:00 PM

“1) Employees are working when they are ill and potentially exposing employees to SARS-CoV-2, the virus that causes COVID-19 by without being tested.

Alleged Hazards: 1, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2021-03-08 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, U.S. POSTAL SERVICE, 3700 RIVERSIDE DRIVE, UPPER ARLINGTON, OH, 43221, USA

U.S. POSTAL SERVICE, 3700 RIVERSIDE DRIVE, UPPER ARLINGTON, OH, 43221, USA

April 1, 2021 12:00 PM

“1. The employer has not taken the appropriate steps to protect employees from SARS-CoV-2, the virus that causes COVID-19 including but not limited to having employees wear facemasks.

Alleged Hazards: 1, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-03-09 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, OhioHealth Rehabilitation Hospital, 1087 Dennison Avenue, COLUMBUS, OH, 43201, USA

OhioHealth Rehabilitation Hospital, 1087 Dennison Avenue, COLUMBUS, OH, 43201, USA

April 1, 2021 12:00 PM

“Complaint: Employees are required to wear N95 respirators while caring for patients that were confirmed to be positive for COVID-19 and medical evaluations and fit testing was not done before employees used the N95 respirators. Findings: Employees who were required to wear respirators had received a... See Morefit test. The medical evaluation form that was being used was inadequate. Citation issued. Complaint: Employees are using bottles of cleaning products that are not labeled. Findings: The cleaning products used had appropriate labeling. No citation issued. Complaint: Eye wash stations were removed. There are bottles to use to flush eyes if needed but they are not readily available. Findings: No corrosive chemicals were used in the workplace, and therefore no eye wash station is required. No citation issued.

Alleged Hazards: 3, Employees Exposed: 70
Source: Osha.gov | Receipt Date: 2020-11-30
See Less
Reported By SafelyHQ.com User

Got the first shot today Pfizer., Columbus, OH, USA

Symptoms: Soreness
Columbus, OH, USA

March 26, 2021 7:02 PM

“Had a firefighter give it to me. I think he administered the shot too high up on the left arm almost into the shoulder joint. Have had many vaccines and shots but never that high up into the arm. Arm is sore. Arm is sore like a tetanus shot Shot administered way too high and the outside of the arm... See Morealmost into the shoulder joint. See Less
Reported By SafelyHQ.com User

Pfizer vaccine causes vertigo, Stow, Ohio, USA

Symptoms: Nausea Fever Headache Dizziness
Stow, Ohio, USA

April 13, 2021 2:50 AM

“My 65 yr old godmother receivers Pfizer vaccine 4/8/21 and states she immediately had such bad vertigo she couldn’t stand. This lasted almost 24 hr. She also complained of fever, intense headache, and nausea. Admits she is hesitant about getting second dose. See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

Covid Vaccine AstraZeneca, Glasgow, UK

Symptoms: Skin Rash Muscle Pain
Glasgow, UK

March 29, 2021 5:06 AM

“After I have my astrazeneca vaccine I had a bad pain in my arm for 4 days but that was not the worst part, I believe the astrazeneca triggered a bad episode of eczema as my skin was fine before the vaccine but shortly after the vaccine my skin started to flair up really badly and I’ve had to go on A... See Morentibiotics. Eczema is caused by an overactive immune response, I believe the astrazeneca triggered a strong immune response and in doing so triggered a outbreak of raw, bleeding skin which became infected and couldn’t Be treated with over the counter creams. I’ve been in severe pain with it for three weeks. I don’t know if it’s a coincidence but I didn’t have any signs of eczema before hand and I was eczema free for over a year. See Less
Reported By SafelyHQ.com User

Pfizer Vaccine, Lafayette, CO, USA

Symptoms: Soreness
Lafayette, CO, USA

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
Reported By SafelyHQ.com User

Modern, Merced County, CA, USA

Symptoms: Other Fatigue
Merced County, CA, USA

March 29, 2021 10:43 PM

“First injection:
No issues with injection and no side effects.
Second injection:
Immediately following injection, blood ran down my arm. They claimed that a vein was punctured, but that the vaccination went in just fine. I questioned them again to make sure. And they insisted it was fine. The f... See Moreirst night following injection, my body was uncomfortable and I was unable to get into a deep sleep. 24hrs after injection, the injection site was surrounded by a large patch of red skin that was hot to the touch. At 28 hours, fatigue and malaise set in. At 48hrs, I felt markedly better, although still fatigued. The injection site was much less inflamed. See Less
Reported By SafelyHQ.com User
SMB Screener

April 9, 2021 6:05 PM

“Company name: NS NY Distributor Inc
Brand name: NS NY Distributor Inc
Product recalled: Premium Orgazen 7000 and Ginseng Power 5000 capsules
Reason of the recall: Undeclared Sildenafil and/or Tadalafil
FDA Recall date: April 09, 2021
Recall details: Company Announcement NS NY Distributor Inc is... See Morevoluntarily recalling all lots within expiry of Premium Orgazen 7000 and Ginseng Power 5000 capsules to the consumer level. FDA  analyses has found the products to contain undeclared sildenafil and/or tadalafil. Sildenafil and tadalafil are known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction. The presence of sildenafil and/or tadalafil in Premium OrgaZen 7000 and Ginseng Power 5000 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 Premium OrgaZen 7000 capsules and Ginseng Power 5000 with undeclared sildenafil and/or 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, NS NY Distributor Inc has not received any reports of adverse events related to this recall.

These tainted products are marketed as a dietary supplements for male sexual enhancement and are packaged in a single capsule blister foil sheet and sold in lots of 3 capsules, 5 capsules and 10 capsules. The affected lot numbers of Premium OrgaZen 7000, UPC 0 40232 18144 3, and Ginseng Power 5000, UPC 0 40232 18144 3 include all lots. Premium OrgaZen 7000 and Ginseng Power 5000 were distributed nationwide in the USA via the internet by seller account Beauty.Kor. and fulfilled by amazon at www.amazon.com.

NS NY Distributor Inc is notifying customers who purchased through Amazon seller account Beauty.Kor by this press announcement. Consumers that have Premium OrgaZen 7000 and Ginseng Power 5000 which are being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact NS NY Distributors Inc by email at NSNYdistributors@gmail.com.

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.

- Complete and submit the report Online.
- Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

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
Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User

April 5, 2021 5:00 PM

“Company name: QMART
Brand name: IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000
Product recalled: Dietary Supplement for male sexual enhancement
Reason of the recall: Undeclared Sildenafil and/or Tadalafil
FDA Recall date: April 05, 2021
Recall det... See Moreails: Company Announcement Elmwood Park, NJ, QMART is voluntarily recalling all lots of IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 to the consumer level. FDA analysis has found the products to be tainted with undeclared sildenafil and/or tadalafil. Sildenafil and tadalafil are ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction. The presence of sildenafil and/or tadalafil in IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 renders them unapproved 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 IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 capsules with undeclared sildenafil and/or 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, QMART has not received any reports of adverse events related to this recall. These tainted products are marketed as dietary supplements for male sexual performance enhancement and are packaged in cardboard blisters. The affected lots of IMPERIAL Gold 2000, PremierZEN Extreme 3000, BURRO en PRIMAVERA 60000 & IMPERIAL Platinum 2000 include all lots. The product can be identified by the UPC codes in the table below which were distributed 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.
Check the full recall details on fda.gov
Source: FDA
See Less
Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Salmonella

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
Reported By SafelyHQ.com User