FDA Drug Recalls

Recalls / Class II

Class IID-1528-2020

Product

Phentermine HCL Blue/Clear capsules, 30mg, packaged in a) 10-count bags (NDC 10702-0028-10), b) 28-count bags (NDC 10702-0028-10) and c) 56-count bags (NDC 10702-0028-10), Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by KVK-Tech Newtown, PA 18940; NDC 10702-0028-10

Affected lot / code info
Lot #: a)19290, Exp. Date: 10/20; b) 19224; Exp. Date: 08/20; 19249, Exp. Date: 09/20; 19290, Exp. Date: 10/20; 19322, Exp. Date: 12/20; 20013, Exp. Date: 01/21; 20039, Exp. Date: 02/21 c) 19290, Exp. Date: 10/20

Why it was recalled

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Recalling firm

Firm
Calvin Scott & Company, Inc.
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
209 Eubank Blvd Ne, N/A, Albuquerque, New Mexico 87123-2745

Distribution

Quantity
N/A
Distribution pattern
Nationwide within the United States

Timeline

Recall initiated
2020-07-27
FDA classified
2020-08-20
Posted by FDA
2020-08-26
Terminated
2024-04-11
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1528-2020. 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