FDA Drug Recalls

Recalls / Class II

Class IID-1430-2016

Product

5 mcg/mL HYDROmorphone HCl and 0.1% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride, 200 mL in 250 mL Hospira LifeCare Bag, Service Code 2H8233, Rx Only, Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC 61553-233-54

Affected lot / code info
Lot Number 160730064M , Exp. Date 6/2/2016 ; Lot Number 160800057M , Exp. Date 6/9/2016 ; Lot Number 160820113M , Exp. Date 6/11/2016 ; Lot Number 160960142M , Exp. Date 6/26/2016 ;

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
90 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-1430-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls