ULTRAtab Laboratories recalls Normed Fem Tablet (Acetaminophen 325 mg, Pamab: 25 mg) bulk containers due to CGMP deviations. Affected units include NDC 62959-701-00, lot 19G077.
CGMP Deviations
ULTRAtab Laboratories is recalling bulk containers of Normed Fem Tablet (Acetaminophen 325 mg, Pamabrom 25 mg) because of CGMP deviations. This means the product may not meet quality standards, though the recall does not specify a risk of injury or harm.
CGMP deviations refer to failures in the manufacturing process that could affect product quality. This means the tablets might not meet safety and quality standards, though the specific hazard is not detailed in the recall notice.
The recall affects bulk containers of Normed Fem Tablet sold by ULTRAtab Laboratories. Healthcare facilities or institutions using this product in bulk are most at risk.
Check for the product code M701L and NDC 62959-701-00 on the container. Bulk lots 19G077 are also affected.
Look for the product code M701L and NDC 62959-701-00 on the container.
The recall mentions CGMP deviations but does not specify any risk of injury or harm.
The recall does not provide specific action steps for consumers; only check product details for affected units.
Check for the product code M701L and NDC 62959-701-00 on the container, and ensure it is a bulk lot 19G077.
We’ve drafted a message you can send ULTRAtab Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0549-2022 — ULTRAtab Laboratories ULTRAtab Laboratories Hello, I own a ULTRAtab Laboratories that is covered by recall D-0549-2022 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.