D-0750-2016 Class II Terminated

Recalled by Hartley Medical Center Pharmacy, Incorporated — Long Beach, CA

FDA drug recall D-0750-2016 was initiated by Hartley Medical Center Pharmacy, Incorporated on February 4, 2016 and is designated Class II. Reason for recall: Lack of Assurance of Sterility The recall status is terminated (terminated August 9, 2016). Affected quantity: 1 syringe.

Recall Details

Product Type
Drugs
Report Date
March 16, 2016
Initiation Date
February 4, 2016
Termination Date
August 9, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1 syringe

Product Description

Hydromorphone HCL 25 mg/ml, vol. 40 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA

Reason for Recall

Lack of Assurance of Sterility

Distribution Pattern

Nationwide. No foreign distribution.

Code Information

BUD: 5/3/2016