Teva recalls Neomycin Sulfate 500mg tablets due to teflon contamination in the active ingredient. Affected lots expire 10/2024. Stop using immediately.
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.
Teva is recalling Neomycin Sulfate 500mg tablets because teflon was found in the active ingredient. This could cause serious injury if the tablets are taken as directed. The recall affects specific lots with expiration dates through October 2024.
Teflon particles in the active ingredient could cause serious injury if taken as directed. The foreign matter may not be visible to the eye and could be harmful when ingested.
People with prescriptions for Neomycin Sulfate 500mg tablets from the recalled lots. Those who have the specific lot numbers (3007830, 3007746, 3007829) and expiration date of 10/2024 are most at risk.
Check for the product name 'Neomycin Sulfate Tablets, USP 500 mg', 100-count bottles, and prescription label. Look for lot numbers 3007830, 3007746, or 3007829 with expiration date 10/2024.
Discard all recalled Neomycin Sulfate 500mg tablets with lot numbers 3007830, 3007746, or 3007829.
Teflon was found in the active ingredient used to make the Neomycin Sulfate Tablets, which could cause serious injury if taken as directed.
Lot numbers 3007830, 3007746, and 3007829 with expiration date 10/2024.
Check for Neomycin Sulfate Tablets, USP 500 mg, 100-count bottles with the specific lot numbers listed above and expiration date 10/2024.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-1473-2022 — Teva Teva Hello, I own a Teva that is covered by recall D-1473-2022 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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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.
