Skip to content
Recall Observatory FDA recall evidence

Drug product

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

D-007-2013

October 03, 2012

Class II

Product summary

Firm
Paddock Laboratories, LLC
Event
Event 63354
Status
Terminated
Classification
Class II
Quantity
2267 bottles
Official record key
drug-enforcement:D-007-2013

Official wording

Reason: 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.

Code information: 2012028142 exp. 1/2014

Distribution pattern: Nationwide

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    dissolution failure