FDA Drug Recalls

Recalls / Class II

Class IID-1014-2013

Product

B-12 REJUV 25 MG/ML INJECTABLE, all configurations, FOR INTRAVENO AND SQ USE ONLY, STERILE, RX ONLY, Compounded by Beacon Hill Medical Pharmacy PC, dba Rxtra Solutions, Southfield, MI

Affected lot / code info
01112013@18, 02112013@8, 03052013@11, 04032013@19, 04122013@34, 05132013@18, 06052013@37, 06212013@14 and 06292013@7

Why it was recalled

Lack of Assurance of Sterility; FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility assurance

Recalling firm

Firm
Beacon Hill Medical Pharmacy, P.C.
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
18161 W 13 Mile Rd, Suite A1, Southfield, Michigan 48076-1113

Distribution

Quantity
N/A
Distribution pattern
USA nationwide

Timeline

Recall initiated
2013-07-26
FDA classified
2013-09-10
Posted by FDA
2013-09-18
Terminated
2014-07-18
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1014-2013. 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