Pregabalin Capsules 300mg 90 recall: CGMP Deviations
PREGABALIN CAPSULES 300MG 90 ; NDC 43598-298-90; RX; CAPSULES
Why was Pregabalin Capsules 300mg 90 recalled?
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
T2000309
- Product
- PREGABALIN CAPSULES 300MG 90 ; NDC 43598-298-90; RX; CAPSULES
- Recalling firm
- Cardinal Health Inc.
- Quantity
- 6 CONTAINERS
- Distribution
- FL, GA, SC
- Recall date
- June 2, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)