FDA Drug Recalls

Recalls / Class II

Class IID-1196-2016

Product

L-CARNITINE 250MG/ML (PF), 10ML Vials, MEDAUS PHARMACY

Affected lot / code info
Lot #: 151123-72, BUD: 05/21/16; Lot #: 151124-33, BUD: 05/22/16; Lot #: 151217-18, BUD: 06/14/16; Lot #: 151217-22, BUD: 06/14/16; Lot #: 151221-3, BUD: 06/18/16; Lot #: 160303-64, BUD: 08/30/16

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Medaus, Inc.
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
6801 Cahaba Valley Rd Ste 116, Birmingham, Alabama 35242-9609

Distribution

Quantity
2250 mL in Vials
Distribution pattern
U.S. Nationwide, Japan, and New Zealand.

Timeline

Recall initiated
2016-05-13
FDA classified
2016-07-08
Posted by FDA
2016-07-20
Terminated
2017-06-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1196-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.