ULTRAtab Laboratories recalls Cystex tablets with CGMP deviations. Affected lots include 18J072 to 19H098. Consumers should check product codes and contact for details.
CGMP Deviations
ULTRAtab Laboratories is recalling Cystex tablets due to manufacturing quality control issues. This recall is for specific lots and product codes, but no immediate danger to users has been identified.
The recall is due to CGMP (Current Good Manufacturing Practices) deviations, which means the tablets were produced without following standard quality control procedures. This could potentially lead to inconsistent medication strength or safety issues, though the exact risk is not specified in the recall.
People who purchased Cystex tablets with the specific product codes listed (M945) from the affected lots (18J072 to 19H098) are likely affected. Those using the product for medical purposes may be at slightly higher risk due to the manufacturing issue.
Check the product code (M945) and lot numbers on the packaging (18J072 to 19H098). The product is sold as a bulk container with specific labeling from ULTRAtab Laboratories in Highland, NY.
Look for product code M945 and lot numbers 18J072 through 19H098 on the packaging.
The recall is due to CGMP deviations, but the official notice does not specify immediate danger to users.
Check the product code (M945) and lot numbers 18J072 to 19H098 on the packaging.
The recall does not specify a remedy, so contact ULTRAtab Laboratories for further instructions.
We’ve drafted a message you can send ULTRAtab Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0555-2022 — ULTRAtab Laboratories ULTRAtab Laboratories Hello, I own a ULTRAtab Laboratories that is covered by recall D-0555-2022 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.
