Teva Pharmaceuticals USA recalls Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 25x2mL Single Dose Vials, Rx only, Distributed by Teva
Teva recalls Metoclopramide injection vials with unknown brown residue inside. Consumers should check vial lot numbers and contact Teva for details.
Stop using this now
Chemical contamination; Unknown brown residue adhering to the inside of one vial.
Contact the company & request your remedy
What happened, in plain English
Teva is recalling Metoclopramide injection vials that may have brown residue inside. This could cause chemical contamination if injected, so affected users should stop using the product and contact Teva for instructions. Read more at govinfonow.com/recall/36513-teva-metoclopramide-injection-recall-brown-residue-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/36513-teva-metoclopramide-injection-recall-brown-residue-risk · Updated October 4, 2026 · FDA enforcement record: FDA #D-0297-2021
Cite this page
“Teva Metoclopramide Injection Recall: Brown Residue Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36513-teva-metoclopramide-injection-recall-brown-residue-risk. Based on FDA recall #D-0297-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0297-2021%22&limit=1).
Why it’s dangerous
The vials may contain an unknown brown residue that could cause chemical contamination when injected. This residue might lead to health issues if the medication is used as intended.
Who’s affected
People with prescriptions for Metoclopramide injection vials with NDC 0703-4502-01 (vial) or 0703-4502-04 (tray). Those who have the vials from lot #31325335B, expiring July 2021, are most at risk.
How to tell if you have this one
Check for vials labeled NDC 0703-4502-01 (vial) or 0703-4502-04 (tray). Look for lot number 31325335B with an expiration date of July 2021.
- Brand
Teva- Category
Drug
What to do — step by step
Stop Using It Now
Immediately stop using the recalled Metoclopramide injection vials if you have them.
Questions people ask
Is this product safe to use?
No, the vials may contain chemical contamination with an unknown brown residue that could cause harm if injected.
How do I check if I have the recalled product?
Check the vial's NDC number: 0703-4502-01 (vial) or 0703-4502-04 (tray), and lot number 31325335B with expiration date July 2021.
What should I do if I have the recalled vials?
Stop using the vials immediately and contact Teva Pharmaceuticals for instructions on disposal.
Contact Teva
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0297-2021 — Teva Teva Hello, I own a Teva that is covered by recall D-0297-2021 from Teva. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-0297-2021 (February 15, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0297-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.