Z-1093-2015 Class II Terminated
FDA device recall Z-1093-2015 was initiated by Stryker Craniomaxillofacial Division on December 17, 2014 and is designated Class II. Reason for recall: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained article #81035 MEDPOR Titan Max OFW - MTB - Left. The appropriate articles were actually included in the shipment. However, the… The recall status is terminated (terminated November 6, 2015). Affected quantity: 1051.
Recall Details
- Product Type
- Devices
- Report Date
- February 18, 2015
- Initiation Date
- December 17, 2014
- Termination Date
- November 6, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1051
Product Description
Reason for Recall
Distribution Pattern
Worldwide Distribution - US Nationwide in the states of PA, KY, VA, CT, UT, MD, AR, FL, TX, AL, DE, IL, IA, MI, CO, OH, GA, CA, DC, MO, LA, WI, ID, SC, NC, NY, MA, NH, CA, OK, MN, KY, IN, OR, TN and the countries of: Argentina, Australia, Canada, Chile, China, Netherlands, France, Spain, South Korea, Colombia, Switzerland, Singapore, and South Africa.