RecallDepth
Class III Terminated

Gabapentin Tablets, USP 600 mg, 500 tablets per bottle, RX Only, Manufactured by ScieGen Pharmaceuticals Inc., Hauppauge, NY 11788, NDC: 50228-177-05.

Company
Sciegen Pharmaceuticals Inc
Recall Initiated
February 17, 2023
Posted
March 8, 2023
Recall Number
D-0354-2023
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
4,392 bottles
Firm Location
Hauppauge, NY, United States

Reason for Recall

Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.

Distribution

Nationwide in the USA and Puerto Rico

Lot / Code Info

Lot # G177092, Exp. 11/24

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