Pantoprazole Sodium Delayed-Release Tablets, USP, 20 mg, Rx Only, 90 tablets per bottle, Manufactured by: Torrent Pharma
Summary
The FDA issued a Class II for Pantoprazole Sodium Delayed-Release Tablets, USP, 20 mg, Rx Only, 90 tablets per by Torrent Pharma Inc. Reason: CGMP deviations: tablets cracking.
Details
Source
Drug Recall
External ID
D-0852-2022
Action Date
2022-05-11
Status
Terminated
Category
drug
Product Description
Pantoprazole Sodium Delayed-Release Tablets, USP, 20 mg, Rx Only, 90 tablets per bottle, Manufactured by: Torrent Pharmaceuticals Ltd., Indrad-382 721, India, Manufactured for: Torrent Pharma Inc., Levittown, PA 19057, NDC# 13668-096-90.
Lot/Code Info: Lot #s: BA34G021, BA34G022, Exp. 09/2022
Quantity Affected: 24,888 bottles
Reason for Recall
CGMP deviations: tablets cracking
Distribution
Nationwide in the U.S.A
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-11
Company
Levittown, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 81 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Torrent Pharma Inc has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Torrent Pharma Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Torrent Pharma Inc have FDA actions?
Torrent Pharma Inc has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0852-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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