Class II · Moderate risk Ongoing
Oxycodone Hydrochloride Tablets
Reason Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
Oxecta
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Failed Impurities/Degradation Specifications
What was recalled
Oxecta(TM) (oxycodone HCl) tablets, 7.5 mg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc. Bristol, TN, NDC 60793-526-01
- Recalling firm
- Pfizer Inc.
- NDC code
- 60793-526-01
- Origin
- NY, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0404-2015
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Oxycodone recalls
See all
Class II · Moderate risk Ongoing
Oxycodone and Acetaminophen CII Tablets USP
Reason Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Class II · Moderate risk Ongoing
Oxycodone and Acetaminophen CII Tablets USP
Reason Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Class III · Low risk Ongoing
Oxaydo
Reason Sub-potent Drug: Lower potency than labeled.
Class II · Moderate risk Terminated
Oxycodone Hydrochloride Oral Solution
Reason Impurity failure at 0-time of the repackaged lot.
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