RemedyRepack Inc. recalls 180-count Ropinirole 2mg tablets (NDC 70518-2750-00) due to cGMP deviations. This medication is prescription-only and may be unsafe if improperly handled.
cGMP Deviations
RemedyRepack Inc. is recalling 180-count Ropinirole 2mg tablets (prescription-only) because of manufacturing quality control issues. This recall affects people who have these specific tablets and may pose safety risks if the product was not handled properly during production.
The recall is due to cGMP deviations, which means the manufacturing process did not meet quality standards. This could potentially lead to unsafe medication if the tablets were not handled correctly during production. However, the exact risk level is not clearly described in the recall notice.
People with a prescription for Ropinirole 2mg tablets who received this specific packaging from RemedyRepack Inc. in Indiana, PA. Those who have the tablets with the lot number B1630017-040122 and expiration date 04/30/2023 are most at risk.
Check for Ropinirole 2mg tablets in 180-count bottles with the lot number B1630017-040122 and expiration date 04/30/2023. These tablets are prescription-only and repackaged by RemedyRepack Inc. in Indiana, PA.
Look for the lot number B1630017-040122 and expiration date 04/30/2023 on the packaging.
The recall states there were cGMP deviations, but the exact safety risk is not clearly described. The manufacturer recommends checking the specific lot number and expiration date.
Check for Ropinirole 2mg tablets in 180-count bottles with the lot number B1630017-040122 and expiration date 04/30/2023.
The recall does not specify a remedy, so you should check with your healthcare provider or the manufacturer for further instructions.
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0499-2023 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0499-2023 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.
