RECALL DATABASE

Metoclopramide Recall: Teva 5 mg bottles

Announced 2026-10-21 · FDA

The recall affects Metoclopramide tablets (5 mg) produced for Teva Pharmaceuticals USA, distributed nationwide in 100- or 500-count bottles (Rx Only). It is due to the presence of foreign tablets/capsules and is classified as moderate severity, involving 240,448 cartons. Specific lots affected include 100-tablet Lots 8634085, 8635085, 8636085 exp 07/2027; and 500-tablet Lot 8633085 exp 07/2027.

BrandTeva Pharmaceuticals USA, Inc
ProductMetoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC 100 Tablets: 0093-2204-01; NDC 500 Tablets: 0093-2204-05
ReasonPresence of Foreign Tablets/Capsules
Severitymoderate
Units affected240448
DistributionUS Nationwide.
AgencyFDA

WHAT YOU SHOULD DO

  1. Check your bottle's lot number and expiry date against the listed lots and dates.
  2. Do not use affected product; set it aside.
  3. Contact Teva or your pharmacist for guidance on replacement or refund and return instructions.
  4. If you have concerns or experience adverse effects, consult your healthcare provider.

How to identify the recalled item

Lot / date codesLot, expiry: [100 Tablets] Lots 8634085, 8635085, 8636085, exp 07/2027; [500 Tablets] Lot 8633085, exp 07/2027
Lot / date codesLot, expiry: [100 Tablets] Lots 8634085, 8635085, 8636085, exp 07/2027; [500 Tablets] Lot 8633085, exp 07/2027

These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.

Other Teva Pharmaceuticals USA, Inc recalls

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This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.