Status
Terminated
Drug Enforcement D-007-2013
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.
Classification
Class II
Report Date
October 17, 2012
Termination Date
November 12, 2013
Product Information
- Product description
- Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,
- Product quantity
- 2267 bottles
- 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.
- Recall initiation reason
- —
- Initial firm notification
- Letter
- Distribution pattern
- Nationwide
Location & Firm
- Recalling firm
- Paddock Laboratories, LLC
- Address
-
3940 Quebec Ave N, N/A
United States - Voluntary / Mandated
- Voluntary: Firm initiated
- Status date
- —
Codes & Dates
- Recall number
- D-007-2013
- Event ID
- 63354
- Recall initiation date
- October 3, 2012
- Center classification date
- October 9, 2012
- Code info
- 2012028142 exp. 1/2014
- More code info
- —