Safecor Recalls Metoclopramide Tablets Due to Co-mingled Tablets
Safecor Health recalls specific lots of 5 mg Metoclopramide tablets due to co-mingled tablets. Check your bottle's lot number and expiry date.
Use caution until it’s fixed
Manufacturer is recalling batches due to co-mingled tablet.
What happened, in plain English
Safecor Health, LLC is recalling batches of Metoclopramide Tablets, USP, 5 mg because the tablets were co-mingled. This means different types or strengths of tablets may have been mixed together in the same bottle. The recall affects products manufactured for Teva Pharmaceuticals. Read more at govinfonow.com/recall/2084747-safecor-health-llc-recalls-metoclopramide-tablets-usp-5-mg-100.
Source Summary by GovInfoNow · govinfonow.com/recall/2084747-safecor-health-llc-recalls-metoclopramide-tablets-usp-5-mg-100 · Published November 10, 2026 · Updated November 11, 2026 · FDA enforcement record: FDA #D-0075-2027
Cite this page
“Safecor Recalls Metoclopramide Tablets Due to Co-mingled Tablets.” GovInfoNow, updated November 11, 2026. https://govinfonow.com/recall/2084747-safecor-health-llc-recalls-metoclopramide-tablets-usp-5-mg-100. Based on FDA recall #D-0075-2027 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0075-2027%22&limit=1).
Why it’s dangerous
Co-mingled tablets can result in patients receiving a different strength or type of medication than prescribed. This could lead to ineffective treatment or adverse effects from taking the wrong dose of Metoclopramide.
Who’s affected
Patients who have purchased Metoclopramide Tablets, USP, 5 mg from nationwide distribution channels between the manufacturing date and the recall announcement. Individuals taking this prescription medication are at risk of receiving incorrect dosages due to the co-mingling.
How to tell if you have this one
Check your bottle for NDC 51079-886-20 and Lot # 3116509 with an expiry date of 07/31/2027. The product is labeled as Rx Only and manufactured for Teva Pharmaceuticals, Parsippany, NJ.
- Brand
Safecor Health- Category
Drug
What to do — step by step
Check Your Bottle
Verify if your bottle matches NDC 51079-886-20 and Lot # 3116509 with expiry 07/31/2027.
Contact Your Pharmacist
Speak with your pharmacist or healthcare provider immediately to determine if you have the recalled product and what steps to take next.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 29 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0075-2027 (October 6, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0075-2027 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on November 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.