FDA recall, , Moderate risk
Safecor Health Metoclopramide Tablets
Manufacturer is recalling batches due to co-mingled tablet.
Summary by Recall Canary from the FDA notice
What happened
Safecor Health, LLC is recalling Metoclopramide Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, manufactured for Teva Pharmaceuticals, Parsippany, NJ 07054, due to a co-mingled tablet. The recall began on October 6, 2026, and was added to the FDA's Enforcement Report on October 23, 2026. The product was distributed nationwide in the US.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is your bottle affected?
Match the NDC and lot code listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
Metoclopramide Tablets, USP, 5 mg, 100 Tablets per bottle
- NDC
- 51079-886-20
- Lot code
- 3116509
Recall details
- Company began the recall
- Sold in
US Nationwide
- Company
- Safecor Health, LLC
- Hazard
- Foreign object
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 100075
- Recall number
- D-0075-2027
All recalls from Safecor Health, LLC
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
