PlainRecalls
FDA Drug Moderate Class II Terminated

Phendimetrazine Yellow Tabs 35mg, packaged in a) 10-count bags (NDC 69543-0410-11) and b) 28-count bags (NDC 69543-0410-11), and c) 56-count bags (NDC 69543-0410-11) Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Virtus Pharm, LLC.

Reported: August 26, 2020 Initiated: July 27, 2020 #D-1522-2020

Product Description

Phendimetrazine Yellow Tabs 35mg, packaged in a) 10-count bags (NDC 69543-0410-11) and b) 28-count bags (NDC 69543-0410-11), and c) 56-count bags (NDC 69543-0410-11) Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Virtus Pharm, LLC.

Reason for Recall

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

Details

Units Affected
N/A
Distribution
Nationwide within the United States
Location
Albuquerque, NM

Frequently Asked Questions

What product was recalled?
Phendimetrazine Yellow Tabs 35mg, packaged in a) 10-count bags (NDC 69543-0410-11) and b) 28-count bags (NDC 69543-0410-11), and c) 56-count bags (NDC 69543-0410-11) Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Virtus Pharm, LLC.. Recalled by Calvin Scott & Company, Inc.. Units affected: N/A.
Why was this product recalled?
CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 26, 2020. Severity: Moderate. Recall number: D-1522-2020.