Z-2331-2012 Class II Terminated

Recalled by Custom Medical Specialties, Inc. — Pine Level, NC

FDA device recall Z-2331-2012 was initiated by Custom Medical Specialties, Inc. on September 30, 2011 and is designated Class II. Reason for recall: The firm saw on the FDA web site a recall by the manufacturer due to no microbial testing in place at the manufacturer and product did not meet proper finished goods specifications. The recall status is terminated (terminated September 10, 2012). Affected quantity: 15 cases.

Recall Details

Product Type
Devices
Report Date
September 19, 2012
Initiation Date
September 30, 2011
Termination Date
September 10, 2012
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
15 cases

Product Description

CMS-2981-R3 Arthrogram Tray containing 2 oz. bottle PVP Prep Solution CMS-2981-R3 Arthrogram Tray containing 2 oz. bottle PVP Prep Solution

Reason for Recall

The firm saw on the FDA web site a recall by the manufacturer due to no microbial testing in place at the manufacturer and product did not meet proper finished goods specifications.

Distribution Pattern

Nationwide Distribution including GA, MI, NY, and PA.

Code Information

14327-0902, 19929-1006