Golden State Alprazolam Tablets Recall: Potential Cross-Contamination Risk
Golden State Medical Supply recalls 1mg Alprazolam tablets due to potential cross-contamination during manufacturing. Affected lots may contain other drugs; contact for return instructions.
Lower-risk recall
CGMP Deviation: Potential cross-contamination with other drug substance during the manufacturing process.
Contact the company
What happened, in plain English
Golden State Medical Supply is recalling 180-count Alpr: 1mg tablets that may have been contaminated during production. This could lead to unintended drug exposure if taken by someone with a sensitivity to other substances. Read more at govinfonow.com/recall/35203-golden-state-alprazolam-tablets-recall-potential-cross-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/35203-golden-state-alprazolam-tablets-recall-potential-cross-contamination-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0654-2022
Cite this page
“Golden State Alprazolam Tablets Recall: Potential Cross-Contamination Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35203-golden-state-alprazolam-tablets-recall-potential-cross-contamination-risk. Based on FDA recall #D-0654-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0654-2022%22&limit=1).
Why it’s dangerous
During manufacturing, the tablets might have been contaminated with other drugs. This could cause unintended reactions in people who are sensitive to those substances, but it's unlikely to cause serious harm.
Who’s affected
People with prescriptions for Alprazolam tablets who received this specific lot number (GS027852) from Golden State Medical Supply. Those with allergies to other medications may be at higher risk.
How to tell if you have this one
Check for the lot number GS027852 on the bottle. The product is 180-count Alprazolam tablets (1mg) with NDC 60429-504-18, sold by Golden State Medical Supply.
- Brand
Golden State Medical Supply- Category
Drug
What to do — step by step
Check Product Details
Look for the lot number GS027852 on the bottle label.
How this recall unfolded
Recall timeline
FDA terminated this recall 6 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #D-0654-2022 (March 2, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0654-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.