Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60
Reported: August 9, 2017 Initiated: July 24, 2017 #D-1056-2017
Product Description
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60
Reason for Recall
Failed Tablet/Capsule Specification; out of specification for tablet weight
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 28,188 bottles
- Distribution
- Nationwide
- Location
- North Wales, PA
Frequently Asked Questions
What product was recalled? ▼
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60. Recalled by Teva Pharmaceuticals USA. Units affected: 28,188 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsule Specification; out of specification for tablet weight
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 9, 2017. Severity: Moderate. Recall number: D-1056-2017.
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