PD-Rx Pharmaceuticals, Inc. recalls PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets NDC 55289-673-24; b) 30 tablets NDC
PD-Rx Pharmaceuticals recalls 200mg ibuprofen tablets with NDC codes 55289-673-24, 55289-673-30, 55289-673-50, and 55289-673-60 due to CGMP deviations. Consumers should check their product labels.
Recall notice
CGMP deviations.
Contact the company & request your remedy
What happened, in plain English
PD-Rx Pharmaceuticals is recalling ibuprofen tablets that were manufactured with CGMP (current good manufacturing practice) deviations. This recall is for safety reasons to prevent potential quality issues with the medication. Read more at govinfonow.com/recall/40908-pd-rx-ibuprofen-200mg-tablets-recall-cgmp-deviations.
Source Summary by GovInfoNow · govinfonow.com/recall/40908-pd-rx-ibuprofen-200mg-tablets-recall-cgmp-deviations · Updated October 7, 2026 · FDA enforcement record: FDA #D-0341-2018
Cite this page
“PD-Rx Ibuprofen 200mg Tablets Recall: CGMP Deviations.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40908-pd-rx-ibuprofen-200mg-tablets-recall-cgmp-deviations. Based on FDA recall #D-0341-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0341-2018%22&limit=1).
Why it’s dangerous
CGMP deviations refer to failures in the manufacturing process that could affect the safety and quality of the medication. These deviations might result in the tablets not meeting the required standards for purity or potency, potentially causing health risks when taken.
Who’s affected
People who purchased PD-Rx Ibuprofen 200mg tablets with the listed NDC codes and expiration dates are affected. Those using these products for pain or inflammation relief may be at risk if the medication does not meet quality standards.
How to tell if you have this one
Check the product label for the NDC codes 55289-673-24, 55289-673-30, 55289-673-50, or 55289-673-60. Also look for expiration dates from the list provided in the recall notice.
- Brand
PD-Rx Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Label
Look for the NDC codes 55289-673-24, 55289-673-30, 55289-673-50, or 55289-673-60 on the packaging.
Questions people ask
Why is this product being recalled?
The recall is due to CGMP deviations, which are manufacturing process failures that could affect the safety and quality of the medication.
What should I do if I have these tablets?
The official recall notice does not specify a remedy, so you should check with PD-Rx Pharmaceuticals for further instructions.
Are there any specific expiration dates I should watch for?
Yes, the affected products have expiration dates listed in the recall, including 5/31/18 and 1/31/18.
Contact PD-Rx Pharmaceuticals
We’ve drafted a message you can send PD-Rx Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0341-2018 — PD-Rx Pharmaceuticals PD-Rx Pharmaceuticals Hello, I own a PD-Rx Pharmaceuticals that is covered by recall D-0341-2018 from PD-Rx Pharmaceuticals. 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-0341-2018 (January 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0341-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.