ETHEX Corporation Initiated Nationwide Voluntary Recall of a Sin...

Courtesy Food and Drug Administration--Recalls  Tue, 12/23/2008 - 17:36

ETHEX Corporation announced today that it has voluntarily recalled to the consumer level, a single production lot of Hydromorphone HCl 2 mg tablets (Lot #90219, Exp: 03/2010; NDC #58177-0620-04), as a precaution, due to the possibility it may contain oversized tablets.

Hydromorphone is a drug used for pain management and is packaged under the ETHEX label in 100-count bottles.

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