FDA Drug Recalls

Recalls / Class II

Class IID-0139-2018

Product

HYDROmorphone 10 mg in 0.9% Sodium Chloride 50 mL PCA, 50 mL Cartridge, Concentration: 0.2 mg/mL., This is a compounded injectable drug; Rx only; Hospital/office use only. SSM St. Clare Outsourcing Facility, Fenton, MO. --- NDC: 88883-0600-01

Affected lot / code info
Lot, exp: 170615-004, 9/13/2017; 170720-009, 10/18/2017

Why it was recalled

Lack of sterility assurance: Microbial growth detected during a routine simulation of the manufacturing process. No batches of distributed product have been identified as actually containing microorganisms.

Recalling firm

Firm
SSM Health Care St. Louis DBA SSM St. Clare Health Center
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
1015 Bowles Ave, N/A, Fenton, Missouri 63026-2394

Distribution

Quantity
N/A
Distribution pattern
SSM Health entities in the state of MO only

Timeline

Recall initiated
2017-08-10
FDA classified
2017-12-28
Posted by FDA
2018-01-03
Terminated
2018-03-22
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0139-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.