PlainRecalls
FDA Drug Moderate Class II Terminated

Quetiapine Tablets USP 400 mg, 100 tablet bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India. Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 --- NDC 67877-248-01, UPC code: 3 67877-248-01 1

Reported: December 5, 2018 Initiated: November 14, 2018 #D-0287-2019

Product Description

Quetiapine Tablets USP 400 mg, 100 tablet bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India. Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 --- NDC 67877-248-01, UPC code: 3 67877-248-01 1

Reason for Recall

Presence of Foreign Substance; metal shard found in tablet

Details

Recalling Firm
Ascend Laboratories LLC
Units Affected
N/A
Distribution
Nationwide
Location
Parsippany, NJ

Frequently Asked Questions

What product was recalled?
Quetiapine Tablets USP 400 mg, 100 tablet bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India. Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 --- NDC 67877-248-01, UPC code: 3 67877-248-01 1. Recalled by Ascend Laboratories LLC. Units affected: N/A.
Why was this product recalled?
Presence of Foreign Substance; metal shard found in tablet
Which agency issued this recall?
This recall was issued by the FDA Drug on December 5, 2018. Severity: Moderate. Recall number: D-0287-2019.