ULTRAtab Laboratories recalls acetaminophen 500mg caplets due to CGMP deviations. Affected lots from Highland, NY NDC 62959-206-00. No specific remedy stated in recall notice.
CGMP Deviations
ULTRAtab Laboratories is recalling acetaminophen 500mg caplets from specific bulk lots due to manufacturing quality control issues. This recall does not include consumer products but affects bulk containers used by pharmacies.
CGMP deviations refer to failures in manufacturing quality control processes. This could mean the caplets may not meet safety standards, though the specific risk is not detailed in the recall notice.
Pharmacies and healthcare facilities that received the bulk container with NDC 62959-206-00 from ULTRAtab Laboratories in Highland, NY. Healthcare workers handling these caplets are most at risk.
Check for the NDC code 62959-206-00 on the bulk container label. The product was manufactured in Highland, NY with lot number 19B002.
Identify the NDC code 62959-206-00 and lot number 19B002 on the bulk container.
No, this recall applies to bulk containers used by pharmacies, not consumer products.
The recall notice does not specify a remedy, so contact ULTRAtab Laboratories for guidance.
The recall mentions CGMP deviations but does not describe specific hazards or injuries.
We’ve drafted a message you can send ULTRAtab Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0534-2022 — ULTRAtab Laboratories ULTRAtab Laboratories Hello, I own a ULTRAtab Laboratories that is covered by recall D-0534-2022 from ULTRAtab Laboratories. 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.