Metoclopramide Tablets recall (Safecor Health, LLC)
DrugClass IIOngoing
Summary: Safecor Health, LLC is recalling Metoclopramide Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 51079-886-20.. Reason: Manufacturer is recalling batches due to co-mingled tablet.
What is being recalled
Metoclopramide Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 51079-886-20.
Why
Manufacturer is recalling batches due to co-mingled tablet.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide
How to tell if yours is affected
Lot # 3116509, Expiry: 07/31/2027.
What to do
Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.
Recall facts
| Recall number | D-0075-2027 |
| Category | Drug |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | October 6, 2026 |
| Reported | November 4, 2026 |
| Company | Safecor Health, LLC |
| Company location | Rockford, IL, United States |
| Initiated by | Voluntary: Firm initiated |
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