RemedyRePack recalls Metformin 750mg Extended Release tablets with NDMA levels above safe limits. Consumers should check product lot numbers and contact the company for a replacement.
CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.
RemedyRePack is recalling Metformin 750 mg Extended Release tablets due to detected N-Nitrosodimethylamine (NDMA) levels exceeding safe limits. This could pose a health risk with long-term use, though the recall does not specify immediate harm.
NDMA is a potential carcinogen that can form in some medications during manufacturing. The recall indicates levels of this chemical were higher than the acceptable limit for safe use in this product.
People who own or use Metformin 750 mg Extended Release tablets with the specified lot numbers. Those with diabetes who take this medication are most at risk.
Check the product label for the lot numbers: J0511265-021121 (exp. 02/28/2022), J0499451-122220 (exp. 01/31/2022), J0496563-120820 (exp. 12/31/2021), or J0495111-120120 (exp. 12/31/2021).
Look for the lot numbers listed in the recall: J0511265-021121, J0499451-122220, J0496563-120820, or J0495111-120120.
Reach out to RemedyRePack for a replacement or refund if you have the recalled product.
The recall indicates NDMA levels exceed safe limits, but the company does not specify immediate health risks. Long-term use could pose a health risk.
Check the product label for the lot numbers: J0511265-021121 (exp. 02/28/2022), J0499451-122220 (exp. 01/31/2022), J0496563-120820 (exp. 12/31/2021), or J0495111-120120 (exp. 12/31/2021).
Contact RemedyRePack for a replacement or refund. The recall does not specify a deadline for action.
We’ve drafted a message you can send RemedyRePack to request your refund or repair — edit it as you like.
Subject: Recall D-0366-2022 — RemedyRePack RemedyRePack Hello, I own a RemedyRePack that is covered by recall D-0366-2022 from RemedyRePack. 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.
