Golden State Medical Supply recalls 10mg Enalapril Maleate tablets (NDC 60429-185-90) due to CGMP deviations. Affected lots expire through 2024; contact for return instructions.
CGMP Deviations
Golden State Medical Supply is recalling 10mg Enalapril Maleate tablets (NDC 60429-185-90) because of manufacturing quality control issues. This recall affects specific production lots that may have been distributed through pharmacies or healthcare providers.
CGMP deviations refer to failures in the manufacturing process that could lead to unsafe medication. While the exact nature of the deviation isn't specified, such issues can potentially cause medication to be ineffective or harmful to patients.
People who have the specific lot numbers listed in the recall (NDC 60429-185-90) and were prescribed this medication. Those with high blood pressure or heart conditions are most at risk if the medication is unsafe.
Check the product label for the NDC code 60429-185-90 and the lot numbers listed (e.g., GS027890 through GS041656). The tablets expire through January 2024.
Look for the NDC code 60429-185-90 and lot numbers from GS027890 to GS041656 on the packaging.
The recall is due to CGMP deviations, but the official notice does not specify if the medication is safe to take. You should not use it until you contact the manufacturer.
Check the product label for the NDC code 60429-185-90 and lot numbers from GS027890 to GS041656.
The official recall notice does not specify a remedy; you should contact Golden State Medical Supply for instructions.
We’ve drafted a message you can send Golden State Medical Supply to request your refund or repair — edit it as you like.
Subject: Recall D-1179-2022 — Golden State Medical Supply Golden State Medical Supply Hello, I own a Golden State Medical Supply that is covered by recall D-1179-2022 from Golden State Medical Supply. 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.
