Walmart Inc recalls Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
Marketed Without An Unapproved NDA/ANDA: All lots were found to be unapproved drugs based on labeling claims.
Read the official notice →- Date
- 2022-06-22
- Country
- United States
- Brand
- Walmart
- Product
- Artri Ajo King Reforzado con Ortiga y Omega 3 Tablets, ORIGINAL, 100-count bottles, UPC 7 501031 12705.
- Classification
- Class II
- Units
- Nationwide in the USA.
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Walmart recalls
- 2025-07-10
US
Walmart Recalls Ozark Trail 64 oz Water Bottles Due to Serious Impact and Laceration Hazards
The lid can forcefully eject, posing serious impact and laceration hazards, when a consumer attempts to open the capped bottles after food, carbonated beverages or perishable beverages, such as juice or milk, are…
- 2025-06-11
US
Walmart Inc recalls Fresh cut cucumber slices, Marketside, packaged in clear plastic circular container with clear plastic lid and white adhesive label with…
Potential Salmonella contamination.
FDA · FoodWalmart Inc12 Retail locations in Texas: Ennis, TX; Palestine, TX; Longview, TX;…Official notice →- 2024-12-18
US
Walmart Inc recalls Marketside Fresh Cut Cucumber Slices. In clear deli plastic container with lid. Weights vary. Perishable. Keep Refrigerated. Distributed…
Sliced cucumbers have the potential to be contaminated with Salmonella.
- 2024-10-23
US
Walmart Inc recalls Great Value Diced Peaches, Mandarin Segments, & Cherry Mixed Fruits Variety Pack, 4 oz, 12 Pack
FD&C Red No 3 was not declared as an ingredient.
- 2022-06-22
US
Walmart Inc recalls Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P.…
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
- 2021-10-22
US
Walmart Recalls Better Homes and Gardens Essential Oil Infused Aromatherapy Room Spray with Gemstones Due to Rare and Dangerous Bacteria; Two Deaths Investigated
Tests conducted by the Centers for Disease Control and Prevention (CDC) determined that a bottle of the room spray contained the rare and dangerous bacteria Burkholderia pseudomallei which causes melioidosis, a…
Other drugs & medical recalls in the United States
- 2022-06-22
US
Illumina, Inc. recalls illumina Model NextSeq 550 Dx REF 20005715
cybersecurity vulnerability
FDA · DeviceIllumina, Inc.Worldwide distribution - U.S. Nationwide distribution including in the states…Official notice →US
Tandem Diabetes Care Inc recalls t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM, and t:slim X2 Insulin Pump with Basal-IQ Technology
Insulin pumps may display unexpected fluctuation of the remaining battery life so ensure pump battery life does not fall below 25% remaining power. If the battery life drops to less than 5%, insulin delivery will…
FDA · DeviceTandem Diabetes Care IncInternational distribution in the country of Australia.Official notice →US
Draeger Medical, Inc. recalls Drager SafeStar 55, Catalog No. MP01790
Possible occlusion of filters due to manufacturing error.
FDA · DeviceDraeger Medical, Inc.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →US
Walmart Inc recalls Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P.…
Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with undeclared diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.
US
Lupin Pharmaceuticals Inc. recalls Zileuton Extended-Release Tablets, 600 mg, 120-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD…
Failed Dissolution Specifications: Out of specification test results observed in dissolution testing during long term stability study.
FDA · DrugLupin Pharmaceuticals Inc.Product was distributed to 10 wholesalers/distributors and one mail order…Official notice →US
Hand Sanitizer LLC recalls HAND SANITIZER SAY GOODBYE TO GERMS Alcohol Antiseptic 80% Topical Non-Sterile Solution, 12 FL OZ (254 mL) bottles, Distributed by: Hand…
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
FDA · DrugHand Sanitizer LLCFirm failed to provide distribution pattern information.Official notice →