FDA Drug Recalls

Recalls / Class II

Class IID-1520-2016

Product

Sennazon (sennosides) Syrup, 8.8 mg, 8 fl. oz. (237 mL) bottle, Mfd. for: Bayshore Pharmaceuticals, Tampla, FL 33619, NDC 76518-100-08.

Affected lot / code info
Lot #: 20391519, Exp 11/17

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
1,008 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-1520-2016. 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