Carisoprodol Tablets, USP, 350 mg, packaged in a) 500-count tablets per bottle (NDC 0143-1176-05) and b) 1000-count tablets per bottle (NDC 0143-1176-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.
Reported: February 13, 2013 Initiated: December 7, 2012 #D-150-2013
Product Description
Carisoprodol Tablets, USP, 350 mg, packaged in a) 500-count tablets per bottle (NDC 0143-1176-05) and b) 1000-count tablets per bottle (NDC 0143-1176-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.
Reason for Recall
Presence of Foreign Substance: Uncharacteristic blacks spots on tablets.
Details
- Recalling Firm
- West-ward Pharmaceutical Corp.
- Units Affected
- 8,585 bottles
- Distribution
- Nationwide
- Location
- Eatontown, NJ
Frequently Asked Questions
What product was recalled? ▼
Carisoprodol Tablets, USP, 350 mg, packaged in a) 500-count tablets per bottle (NDC 0143-1176-05) and b) 1000-count tablets per bottle (NDC 0143-1176-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.. Recalled by West-ward Pharmaceutical Corp.. Units affected: 8,585 bottles.
Why was this product recalled? ▼
Presence of Foreign Substance: Uncharacteristic blacks spots on tablets.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 13, 2013. Severity: Moderate. Recall number: D-150-2013.
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