Recalls / Class II
Class IID-007-2013
Product
Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,
- Affected lot / code info
- 2012028142 exp. 1/2014
Why it was recalled
Paddock Laboratories, LLC are recalling one lot (2012028142) of Moexipril HCl Tablets 7.5mg (expiration 1/2014) because of a non-conformity dissolution failure result found during routine stability testing at the 6 month test interval.
Recalling firm
- Firm
- Paddock Laboratories, LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 3940 Quebec Ave N, N/A, Minneapolis, Minnesota 55427-1244
Distribution
- Quantity
- 2267 bottles
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2012-10-03
- FDA classified
- 2012-10-09
- Posted by FDA
- 2012-10-17
- Terminated
- 2013-11-12
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-007-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.