ULTRAtab Laboratories recalls caffeine tablets due to manufacturing deviations. Consumers should check product codes and NDC numbers for affected lots.
CGMP Deviations
ULTRAtab Laboratories is recalling caffeine tablets that may have manufacturing deviations. This could affect product safety, though the specific risk isn't detailed in the recall notice.
The recall mentions CGMP (Current Good Manufacturing Practices) deviations, which are regulatory standards for safe production. However, the specific nature of the deviation and its potential impact on safety are not described in the notice.
Anyone who owns or uses ULTRAtab's caffeine tablets with the listed NDC numbers and product codes. People who consume these tablets regularly are most at risk.
Check for NDC number 62959-941-00 and product codes M941L or M940LA on the packaging. Affected lots include 19C065, 19F081, 19H083, and 17D088.
Look for NDC number 62959-941-00 and product codes M941L or M940LA on the packaging.
The recall is due to CGMP deviations, but the specific nature of the deviation and its safety impact are not detailed in the notice.
The recall notice does not specify a remedy, so check the product details and contact ULTRAtab Laboratories if you have concerns.
Affected lots include 19C065, 19F081, 19H083, and 17D088.
We’ve drafted a message you can send ULTRAtab to request your refund or repair — edit it as you like.
Subject: Recall D-0554-2022 — ULTRAtab ULTRAtab Hello, I own a ULTRAtab that is covered by recall D-0554-2022 from ULTRAtab. 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.
