Rubicon Research recalls 50mg tramadol tablets (1000-count) with foreign baclofen tablets found in some bottles. This Rx-only medication was distributed by Advagen Pharma in the US. Consumers should contact the manufacturer for details.
Presence of Foreign Tablets: Pharmacist reported a tablet of baclofen in a bottle of 1000-count tramadol
Rubicon Research is recalling 50mg tramadol hydrochloride tablets (1000-count) because a pharmacist found baclofen tablets inside some bottles. This is a serious safety issue as the foreign medication could cause unintended effects if taken.
The hazard involves foreign baclofen tablets being present in some bottles of tramadol. Baclofen is a different medication that could interact with tramadol or cause unintended side effects if taken together. This is a serious safety issue because the foreign tablets were not intended to be in the product.
People who have the 1000-count tramadol tablets with NDC 72888-080-00 and lot number 230774Hl from the US distribution by Advagen Pharma are affected. Those who have taken the foreign baclofen tablets could be at risk.
Check for the product name 'traMADol Hydrochloride Tablets, USP 50 mg, 1000-count bottle' with NDC 72888-080-00 and lot number 230774Hl. The product was distributed by Advagen Pharma in the US and manufactured by Rubicon Research in India.
Look for the NDC code 72888-080-00 and lot number 230774Hl on the bottle label.
A pharmacist reported finding baclofen tablets inside some bottles of tramadol, which could cause unintended effects if taken.
The recall record does not specify a remedy, so consumers should contact the manufacturer for details.
Check for the NDC code 72888-080-00 and lot number 230774Hl on the bottle label.
We’ve drafted a message you can send Rubicon Research to request your refund or repair — edit it as you like.
Subject: Recall D-0487-2024 — Rubicon Research Rubicon Research Hello, I own a Rubicon Research that is covered by recall D-0487-2024 from Rubicon Research. 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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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.
