Zimmer Inc. Zimmer Dermacarriers II skin graft carriers, 1.5 to 1 dermacarrier, Rx, latex free, sterile, Zimmer, Dover, Ohio; REF 00-2195-012-00. Single use device for use during skin grafting procedures. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zimmer Dermacarriers II skin graft carriers, 1.5 to 1 dermacarrier, Rx, latex free, sterile, Zimmer, Dover, Ohio; REF 00-2195-012-00. Single use device for use during skin grafting procedures.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
All lots.
Products Sold
All lots.
Zimmer Inc. is recalling Zimmer Dermacarriers II skin graft carriers, 1.5 to 1 dermacarrier, Rx, latex free, sterile, Zimmer, due to Sterility compromised. Lack of assurance of sterility, as the packages may not have been sealed on the manufacturer's end.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterility compromised. Lack of assurance of sterility, as the packages may not have been sealed on the manufacturer's end.
Recommended Action
Per FDA guidance
Consignees were notified via letter (Urgent: Medical Device Correction) dated 4/3/08 to identify their stocks on hand, verify package sealing, to discard any non-sealed packages, mail the Business Reply Card regardless if there are any remaining affected products.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026