Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to Chemical contamination; Unknown brown residue adhering to the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teva Pharmaceuticals USA directly.
Affected Products
Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 25x2mL Single Dose Vials, Rx only, Distributed by Teva Pharmaceuticals, USA, Inc., Parsippany, NJ Vial NDC 0703-4502-01 (vial) NDC# 0703-4502-04 (tray)
Quantity: 9,452 cartons
Why Was This Recalled?
Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA
Teva Pharmaceuticals USA has 196 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report