PlainRecalls
FDA Drug Moderate Class II Terminated

Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,

Reported: October 17, 2012 Initiated: October 3, 2012 #D-007-2013

Product Description

Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,

Reason for Recall

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.

Details

Recalling Firm
Paddock Laboratories, LLC
Units Affected
2267 bottles
Distribution
Nationwide
Location
Minneapolis, MN

Frequently Asked Questions

What product was recalled?
Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,. Recalled by Paddock Laboratories, LLC. Units affected: 2267 bottles.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 17, 2012. Severity: Moderate. Recall number: D-007-2013.