American Pharmaceutical Ingredients LLC recalls Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000
CGMP Deviations: Lack of quality assurance at the API manufacturer.
Recall notice
CGMP Deviations: Lack of quality assurance at the API manufacturer.
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We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
Source Page by GovInfoNow · govinfonow.com/recall/41594-american-pharmaceutical-ingredients-llc-recalls-methocarbamol-usp-packaged-in-a · Recall date May 26, 2017 · FDA enforcement record: FDA #D-0937-2017
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“American Pharmaceutical Ingredients LLC recalls Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000.” GovInfoNow, recall dated May 26, 2017. https://govinfonow.com/recall/41594-american-pharmaceutical-ingredients-llc-recalls-methocarbamol-usp-packaged-in-a. Based on FDA recall #D-0937-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0937-2017%22&limit=1).
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Contact American Pharmaceutical Ingredients LLC
We’ve drafted a message you can send American Pharmaceutical Ingredients LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0937-2017 — American Pharmaceutical Ingredients LLC American Pharmaceutical Ingredients LLC recalls Methocarbam Hello, I own a American Pharmaceutical Ingredients LLC recalls Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 that is covered by recall D-0937-2017 from American Pharmaceutical Ingredients LLC. 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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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-0937-2017 (May 26, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0937-2017 to see it in context.
- 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.