ULTRAtab Back Relief II Tablets Recall: CGMP Deviations Risk

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Contact the company & request your remedy

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

ULTRAtab Laboratories is recalling Back Relief II tablets (Acetaminophen 200 mg, Magnesium Salicylate 200 mg) because of manufacturing quality control issues. This recall affects specific lots produced in Highland, NY, and may pose risks related to product safety.

Why it’s dangerous

CGMP deviations refer to failures in manufacturing quality control processes. This could mean the tablets may not meet safety standards, potentially leading to health risks if used improperly.

Who’s affected

People who purchased Back Relief II tablets from Highland, NY. Those with the specific NDC code 62959-740-00 or product codes M740LA are most at risk.

How to tell if you have this one

Check for the NDC code 62959-740-00 or product codes M740LA on the container. The affected lots are 19C022 and 19C023 from Highland, NY.

Brand
ULTRAtab
Category
Drug

Based on the official FDA remedy

What to do — step by step

Contact Manufacturer
ULTRAtab Laboratories will provide details on how to handle the recalled product through their official channels.

✎ GovInfoNow

Questions people ask

What is the product being recalled?

Back Relief II (Acetaminophen 200 mg, Magnesium Salicylate 200 mg) Bulk Container from ULTRAtab Laboratories, Inc.

What lots are affected?

Bulk Lots: 19C022, 19C023

How can I check if I have the recalled product?

Look for NDC code 62959-740-00 or product codes M740LA on the container.

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-0551-2022 — ULTRAtab ULTRAtab

Hello,

I own a ULTRAtab that is covered by recall D-0551-2022 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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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-0551-2022 (January 26, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0551-2022 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 Back Relief II (Acetaminophen 200 mg, Magnesium Salicylate 200 mg) Bulk Container, ULTRAtab Laboratories, Inc.,

Recall notice