FDA Drug Recalls

Recalls / Class II

Class IID-1361-2016

Product

0.05 mg/mL Morphine Sulfate and 0.0625% Bupivacaine HCI (Preservative Free) in 0.9% Sodium Chloride, 250 mL Hospira LifeCare bag, Rx Only, Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC 61553-995-54 ,

Affected lot / code info
Lot # 160420165M; Exp. 05/16 Lot # 160540128M; Exp. 05/16 Lot # 160630117M; Exp. 06/16 Lot # 160770157M; Exp. 06/16 Lot # 160870055M; Exp. 06/16 Lot # 160890153M; Exp. 06/16 Lot # 160950340M; Exp. 07/16

Why it was recalled

Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.

Recalling firm

Firm
Pharmedium Services, LLC
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
150 N Field Dr Ste 350, N/A, Lake Forest, Illinois 60045-2506

Distribution

Quantity
80 bags
Distribution pattern
Nationwide

Timeline

Recall initiated
2016-05-05
FDA classified
2016-07-16
Posted by FDA
2016-07-27
Terminated
2018-03-06
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1361-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.