East Brunswick, NJ – A nationwide drug recall has been issued after a serious labeling mistake that could put some patients’ health at risk.
Unichem Pharmaceuticals, based in New Jersey, is recalling one batch of its Cyclobenzaprine 10mg tablets—a muscle relaxer—after discovering that the bottles were filled with Meloxicam 7.5mg, a medication used to treat arthritis. The two drugs are very different, and taking the wrong one can lead to dangerous side effects.
According to the company, the mix-up involves bottles labeled Cyclobenzaprine Hydrochloride Tablets USP, 10mg, with lot number GMML24026A and an expiration date of September 2027. Instead of the expected blue muscle relaxer pills, these bottles may contain light yellow tablets of Meloxicam.
For someone who isn’t expecting to take Meloxicam, the risks can be serious. Possible reactions include stomach bleeding, kidney damage, heart complications, or severe allergic responses—especially in people who are already taking other medications like blood thinners or NSAIDs.
So far, no injuries or illnesses have been reported, but the company and the FDA are urging caution. The product was shipped nationwide and may already be in the hands of consumers.
What You Should Do:
- If you have a prescription for Cyclobenzaprine 10mg, check the label for lot number GMML24026A.
- If it matches, do not take the medication.
- Return the bottle to the pharmacy where you got it and ask for a replacement.
- If you’ve already taken the pills and feel unwell, call your doctor immediately.
Pharmacies and distributors are being asked to stop selling or dispensing this lot and to notify any affected customers.
Questions about the recall can be directed to Inmar at 1-877-840-5109 or rxrecalls@inmar.com, Monday through Friday, 9 a.m. to 5 p.m. CST.
This article was produced by a journalist and may include AI‑assisted input. All content is reviewed for accuracy and fairness.
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