PlainRecalls
FDA Drug Moderate Class II Terminated

PREGABALIN CAPSULES 300MG 90 ; NDC 43598-298-90; RX; CAPSULES

Reported: June 2, 2021 Initiated: March 15, 2021 #D-0469-2021

Product Description

PREGABALIN CAPSULES 300MG 90 ; NDC 43598-298-90; RX; CAPSULES

Reason for Recall

CGMP Deviations: Intermittent exposure to temperature excursion during storage.

Details

Recalling Firm
Cardinal Health Inc.
Units Affected
6 CONTAINERS
Distribution
FL, GA, SC
Location
Dublin, OH

Frequently Asked Questions

What product was recalled?
PREGABALIN CAPSULES 300MG 90 ; NDC 43598-298-90; RX; CAPSULES. Recalled by Cardinal Health Inc.. Units affected: 6 CONTAINERS.
Why was this product recalled?
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 2, 2021. Severity: Moderate. Recall number: D-0469-2021.