RemedyRepack TraMADol HCl 50mg Tablets: Foreign Baclofen Risk
RemedyRepack recalls 30-count and 90-count blister packs of TraMADol HCl 50mg tablets due to potential presence of baclofen tablets. Consumers should check their product details and contact the manufacturer for guidance.
Lower-risk recall
Presence of Foreign Tablets: Manufacturer received a report from a Pharmacist who reported finding a tablet of baclofen in a bottle of 1000-count tramadol
Contact the company
What happened, in plain English
RemedyRepack is recalling specific packs of TraMADol HCl 50mg tablets after a pharmacist reported finding baclofen tablets in some bottles. This could lead to unintended medication intake and health risks. Read more at govinfonow.com/recall/32694-remedyrepack-tramadol-hcl-50mg-tablets-foreign-baclofen-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/32694-remedyrepack-tramadol-hcl-50mg-tablets-foreign-baclofen-risk · Updated September 23, 2026 · FDA enforcement record: FDA #D-0489-2024
Cite this page
“RemedyRepack TraMADol HCl 50mg Tablets: Foreign Baclofen Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32694-remedyrepack-tramadol-hcl-50mg-tablets-foreign-baclofen-risk. Based on FDA recall #D-0489-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0489-2024%22&limit=1).
Why it’s dangerous
The hazard involves foreign tablets of baclofen being present in some bottles of TraMADol HCl 50mg. This could cause unintended medication intake if someone takes the wrong tablet, potentially leading to health issues.
Who’s affected
People who have the 30-count or 90-count blister packs of TraMADol HCl 50mg tablets from RemedyRepack. Those with the product may be at risk if they accidentally take the foreign baclofen tablets.
How to tell if you have this one
Check for the product names: TraMADol HCl 50mg Tablets. Look for the specific blister pack counts: 30-count or 90-count. The NDC numbers are 70518-3824-00 or 70518-3824-02.
- Brand
RemedyRepack- Category
Drug
What to do — step by step
Check Product Details
Look for the 30-count or 90-count blister packs with NDC numbers 70518-3824-00 or 70518-3824-02.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest drug recalls
Keep exploring
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-0489-2024 (May 2, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0489-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.