Lisinopril and Hydrochlorothiazide Tablets, 20 mg/25 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1264-01) and b) 1000-count tablets per bottle (NDC 0143-1264-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.
Reported: January 30, 2013 Initiated: November 30, 2012 #D-132-2013
Product Description
Lisinopril and Hydrochlorothiazide Tablets, 20 mg/25 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1264-01) and b) 1000-count tablets per bottle (NDC 0143-1264-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.
Reason for Recall
Presence of Foreign Substance: Reports of gray smudges identified as minute stainless steel particulates were found in the recalled tablets.
Details
- Recalling Firm
- West-ward Pharmaceutical Corp.
- Units Affected
- 43,478 bottles
- Distribution
- Nationwide and Puerto Rico
- Location
- Eatontown, NJ
Frequently Asked Questions
What product was recalled? ▼
Lisinopril and Hydrochlorothiazide Tablets, 20 mg/25 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1264-01) and b) 1000-count tablets per bottle (NDC 0143-1264-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.. Recalled by West-ward Pharmaceutical Corp.. Units affected: 43,478 bottles.
Why was this product recalled? ▼
Presence of Foreign Substance: Reports of gray smudges identified as minute stainless steel particulates were found in the recalled tablets.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 30, 2013. Severity: Moderate. Recall number: D-132-2013.
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