FDA Drug Recalls

Recalls / Class II

Class IID-1526-2016

Product

Senna Syrup (sennosides) 8.8 mg, 8 fl. oz. (237 mL) bottle, Distributed by: Major Pharmaceuticals, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0904-6289-09.

Affected lot / code info
Lot #: 20391517, Exp 09/17; 20391518, Exp10/17; 20391519, Exp 11/17; 20391601, Exp 01/18; 20391602, Exp 02/18; 20391604, 20391605, Exp 03/18; 20391608, Exp 06/18

Why it was recalled

CGMP Deviations: Recall initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia.

Recalling firm

Firm
Pharmatech LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
4131 Sw 47th Ave, Suite 1403, Davie, Florida 33314-4026

Distribution

Quantity
68,908 bottles
Distribution pattern
Nationwide

Timeline

Recall initiated
2016-08-08
FDA classified
2016-09-27
Posted by FDA
2016-10-05
Terminated
2024-09-23
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1526-2016. 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