ULTRAtab Pain Aid PMF Caplets: CGMP Deviations Risk

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 is recalling bulk containers of Pain Aid PMF Caplets (Acetaminophen 500 mg, Pamabrom 25 mg) because of manufacturing quality control issues. This recall affects people who have the specific bulk container model from Highland, NY.

Why it’s dangerous

CGMP deviations refer to failures in the manufacturing process that could lead to unsafe products. While the exact risk isn't specified, such deviations might affect the product's safety and quality.

Who’s affected

People who have the bulk container of Pain Aid PMF Caplets with NDC 62959-710-00 from ULTRAtab Laboratories, Inc. in Highland, NY are affected. Those using the product for pain relief may be at risk due to the manufacturing issue.

How to tell if you have this one

Check for the NDC code 62959-710-00 on the bulk container. The product was manufactured in Highland, NY by ULTRAtab Laboratories, Inc. and sold in bulk lots labeled 19A071.

Brand
ULTRAtab
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the NDC code 62959-710-00 on the bulk container label.

✎ GovInfoNow

Questions people ask

What is the product name?

Pain Aid PMF Caplets (Acetaminophen 500 mg, Pamabrom 25 mg).

Why is this product being recalled?

Due to CGMP deviations in manufacturing.

How can I tell if I have the recalled product?

Check for the NDC code 62959-710-00 on the bulk container label.

Take action

Contact ULTRAtab

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

✉️ Open in email

Subject: Recall D-0550-2022 — ULTRAtab ULTRAtab

Hello,

I own a ULTRAtab that is covered by recall D-0550-2022 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.

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-0550-2022 (January 26, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0550-2022 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 Pain Aid PMF Caplet (Acetaminophen 500 mg, Pamabrom 25 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY

Recall notice