Safety Alerts & Recalls

What does this mean?

This recall for Percocet (oxycodone and acetaminophen tablets, USP) 10 mg/325 mg was issued at a warehouse and pharmacy level only. The FDA and the manufacturer have determined that any recalled product that may have been dispensed to patients does not pose a significant health risk. If you take Percocet (oxycodone and acetaminophen tablets, USP) 10 mg/325 mg and your prescription bottle contains different tablets, it's a good idea to take your bottle to your pharmacy and speak to your pharmacist. If you have other concerns about your medicine or think you are experiencing side effects, please follow up with your doctor or other healthcare provider.

Endo Pharmaceuticals Recalls Single Lot of Percocet 10 mg/325 mg

Endo Pharmaceuticals has recalled a single lot of Percocet (oxycodone and acetaminophen tablets, USP) 10 mg/325 mg. Lot number 402243NV is being recalled because a different tablet with the same active ingredients (Endocet 10/325 mg) was found in a bottle from this lot.

Percocet contains the active ingredients oxycodone and acetaminophen and is commonly used in the treatment of pain. Oxycodone and acetaminophen is also sold under the brand name Endocet, Oxycet, and Roxicet. This recall alert only applies to the single lot of Percocet (oxycodone and acetaminophen tablets, USP) 10 mg/325 mg. No other oxycodone and acetaminophen products were involved in this recall.

To view the FDA notice about this recall, please visit: more information here

Source: FDA
Publication Date: 2011-06-14
Last Updated: 2011-06-14

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