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Zimmer Surgical Inc recalls Zimmer¿ Air Dermatome II Width Plate, 1.5 inch. Part #00-8851-215-00. Width plate is packaged inside of a padded-foa
Recalled August 10, 2016 · FDA recall Z-2338-2016 · Zimmer Surgical
Hazard
The surface coating applied to the device is blistering, peeling and discoloring after usage over time · FDA Class II
Units
60 units
Sold at
US Nationwide Distribution including states of: AL, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, and WI.
Description
The surface coating applied to the device is blistering, peeling and discoloring after usage over time
Product
Zimmer¿ Air Dermatome II Width Plate, 1.5 inch. Part #00-8851-215-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or padded envelope. The Zimmer Air Dermatome II is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities.
Manufacturer(s)
Zimmer Surgical Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →