Teva Pharmaceuticals USA recalls Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories,
Failed Dissolution Specifications: Low out of specification results for dissolution.
Recall notice
Failed Dissolution Specifications: Low out of specification results for dissolution.
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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/41136-teva-pharmaceuticals-usa-recalls-methylphenidate-hydrochloride-tablets-usp-20-mg · Recall date October 17, 2017 · FDA enforcement record: FDA #D-0052-2018
Cite this page
“Teva Pharmaceuticals USA recalls Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories,.” GovInfoNow, recall dated October 17, 2017. https://govinfonow.com/recall/41136-teva-pharmaceuticals-usa-recalls-methylphenidate-hydrochloride-tablets-usp-20-mg. Based on FDA recall #D-0052-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0052-2018%22&limit=1).
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Teva Pharmaceuticals USA- Category
Drug
Contact Teva Pharmaceuticals USA
We’ve drafted a message you can send Teva Pharmaceuticals USA to request your refund or repair — edit it as you like.
Subject: Recall D-0052-2018 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA recalls Methylphenidate Hydrochloride Tablets USP Hello, I own a Teva Pharmaceuticals USA recalls Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, that is covered by recall D-0052-2018 from Teva Pharmaceuticals USA. 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-0052-2018 (October 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0052-2018 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.
