Golden State Medical Supply recalls 10mg Paroxetine tablets (NDC 60429-734-30, 90-count, 1000-count) manufactured by Apotex Inc. due to failed impurities testing. Rx-only medication.
Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine
Golden State Medical Supply is recalling 10mg Paroxetine tablets from specific bottle counts and lot numbers because the manufacturing process failed impurities tests. This could lead to unsafe drug levels in the medication.
The medication failed impurities testing, meaning the drug may contain unsafe levels of a chemical byproduct. This could cause adverse effects in patients taking the medication.
People with prescriptions for Paroxetine 10mg tablets from the recalled lot numbers and bottle counts. Those who have taken the medication without checking the lot numbers are at risk.
Check the bottle count (30-count, 90-count, or 1000-count) and lot numbers (GS041383, GS042141, etc.) on the packaging. The expiration date is August 31, 2024.
Verify the bottle count and lot numbers on the packaging to confirm if it's part of the recall.
The manufacturer Apotex Inc. found the medication failed impurities testing, which could lead to unsafe drug levels.
Check the bottle count and lot numbers to confirm if it's part of the recall. If it is, contact your healthcare provider for guidance.
The recall indicates potential safety issues, so it's recommended to check if you have the recalled product before using.
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-0128-2024 — Golden State Medical Supply Golden State Medical Supply Hello, I own a Golden State Medical Supply that is covered by recall D-0128-2024 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.
