FDA Drug Recalls

Recalls / Class II

Class IID-0090-2015

Product

Hydromorphone HCl (PF) 1 mg/mL injectable packaged in 30 mL or 60 mL syringes, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.

Affected lot / code info
Lot Number: 08182014@41, Exp 11/16/2014

Why it was recalled

Lack of Assurance of Sterility: Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all compounded sterile preparations within expiry. The recall is being initiated in connection with a recent FDA inspection due to observations associated with certain quality control procedures that present a risk to sterility assurance.

Recalling firm

Firm
Martin Avenue Pharmacy, Inc.
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
1247 Rickert Dr, N/A, Naperville, Illinois 60540-1008

Distribution

Quantity
20 mL
Distribution pattern
Nationwide

Timeline

Recall initiated
2014-08-27
FDA classified
2014-10-29
Posted by FDA
2014-11-05
Terminated
2018-05-31
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0090-2015. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.