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Class II Recall Active for Hydromorphone
05/09/2019
The recall affect bags of the compounded drug from lot 01/14/19 0215 22110P (Exp. 04/29/2019). The recalled bags were distributed throughout the United States.
Advanced Pharma voluntarily issued the recall April 26, 2019. On April 29, 2019, the FDA designated it Class II, signaling use of the product could cause temporary or medically reversible adverse health consequences. A remote possibility of serious harm also exists.
Hydromorphone is a narcotic medication used to relieve pain.
—Jolynn Tumolo
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