ULTRAtab Coated APAP 325mg Bulk Container Recall: CGMP Deviations

Take action

Contact the company & request your remedy

Recalling firmULTRAtab Laboratories, Inc.50 Toc Dr, N/A · Highland, NY 12528-1506

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

ULTRAtab Laboratories is recalling a bulk container of 325mg acetaminophen tablets (NDC 62959-202-00) because of manufacturing quality control issues. This recall affects specific production lots and may pose risks related to product safety standards.

Why it’s dangerous

CGMP deviations refer to failures in the manufacturing process that could lead to unsafe products. While the exact nature of the deviation isn't specified, such issues may compromise product quality and safety standards.

Who’s affected

This recall affects healthcare facilities or institutions that use bulk acetaminophen tablets for medical purposes. Individuals using these tablets in a clinical setting are most at risk.

How to tell if you have this one

Check for the product code L202L on the container. Affected lots include 18K013 through 19H074. The NDC number 62959-202-00 identifies this specific product.

Brand
ULTRAtab Laboratories
Category
Drug

Based on the official FDA remedy

What to do — step by step

Contact Manufacturer
ULTRAtab Laboratories should be contacted for specific instructions on handling the recalled product.

✎ GovInfoNow

Questions people ask

What is the product code for the recalled tablets?

The product code is L202L.

Which lots are affected by this recall?

Affected lots include 18K013, 18K014, 18K015, 19A040, 18M076, 19A041, 19H072, 19H073, and 19H074.

Is there a specific remedy for this recall?

The recall record does not specify a remedy.

Take action

Contact ULTRAtab Laboratories

We’ve drafted a message you can send ULTRAtab Laboratories to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0532-2022 — ULTRAtab Laboratories ULTRAtab Laboratories

Hello,

I own a ULTRAtab Laboratories that is covered by recall D-0532-2022 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-0532-2022 (January 26, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0532-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
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.

ULTRAtab Laboratories, Inc. recalls Coated APAP 325mg (Acetaminophen 325 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY NDC 62959-202-00

Recall notice