Gabapentin Tablets, USP 600 mg, 500 tablets per bottle, RX Only, Manufactured by ScieGen Pharmaceuticals Inc., Hauppauge, NY 11788, NDC: 50228-177-05.
Reported: March 8, 2023 Initiated: February 17, 2023 #D-0354-2023
Product Description
Gabapentin Tablets, USP 600 mg, 500 tablets per bottle, RX Only, Manufactured by ScieGen Pharmaceuticals Inc., Hauppauge, NY 11788, NDC: 50228-177-05.
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.
Details
- Recalling Firm
- Sciegen Pharmaceuticals Inc
- Units Affected
- 4,392 bottles
- Distribution
- Nationwide in the USA and Puerto Rico
- Location
- Hauppauge, NY
Frequently Asked Questions
What product was recalled? ▼
Gabapentin Tablets, USP 600 mg, 500 tablets per bottle, RX Only, Manufactured by ScieGen Pharmaceuticals Inc., Hauppauge, NY 11788, NDC: 50228-177-05.. Recalled by Sciegen Pharmaceuticals Inc. Units affected: 4,392 bottles.
Why was this product recalled? ▼
Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 8, 2023. Severity: Low. Recall number: D-0354-2023.
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