Dermacarriers 00-7716-000-10Recalls & reported problems
Zimmer Orthopaedic Surgical Products, Inc. · ZIMMER SKIN GRAFT CARRIER 16 inch LENGTH · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00889024375499), received between Dec 19, 2024 and Jul 16, 2025 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Delivered as Unsterile Product” (6 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Delivered as Unsterile Product6
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 16, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
IT WAS REPORTED THAT DURING INCOMING INSPECTION A HAIR LIKE SUBSTANCE WAS FOUND IN THE PACKAGE OF TWO DEVICES. NO HARM OR SURGICAL DELAY OCCURRED AS THERE WAS NO PATIENT INVOLVEMENT. DUE DILIGENCE IS COMPLETE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22519969 ↗MalfunctionJul 16, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
IT WAS REPORTED THAT DURING INCOMING INSPECTION A HAIR LIKE SUBSTANCE WAS FOUND IN THE PACKAGE OF TWO DEVICES. NO HARM OR SURGICAL DELAY OCCURRED AS THERE WAS NO PATIENT INVOLVEMENT. DUE DILIGENCE IS COMPLETE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22519933 ↗MalfunctionJul 16, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
IT WAS REPORTED THAT DURING INCOMING INSPECTION AN UNKNOWN FOREIGN SUBSTANCE WAS FOUND IN THE PACKAGE. NO HARM OR SURGICAL DELAY OCCURRED AS THERE WAS NO PATIENT INVOLVEMENT. DUE DILIGENCE IS COMPLETE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22519929 ↗MalfunctionJan 30, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
UPON RECEIPT OF ADDITIONAL INFORMATION, IT WAS DETERMINED THIS PRODUCT SHOULD NOT HAVE BEEN REPORTED SINCE THE DEBRIS WAS WITHIN SPECIFICATION AND THE PACKAGE WAS CONFORMING. THIS MEDWATCH IS BEING VOIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277519 ↗MalfunctionJan 30, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
IT WAS REPORTED DURING THE INCOMING INSPECTION, A TEAM MEMBER FOUND FOREIGN SUBSTANCE. THERE WAS NO PATIENT INVOLVEMENT. DUE DILIGENCE IS COMPLETE, THERE IS NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277509 ↗MalfunctionDec 19, 2024Delivered as Unsterile Product; Delivered as Unsterile Product
THERE IS NO ADDITIONAL INFORMATION REGARDING THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20983353 ↗
Other Expander, Surgical, Skin Graft devices
- N/A 00-7701-000-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft521 reports
- N/A 00-7703-015-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft206 reports
- N/A 00-7703-020-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft103 reports
- MeshgraftTM II Tissue Expansion System 00-2195-013-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft1 recall30 reports
- MESHGRAFT™ 00-2195-000-00Zimmer Orthopaedic Surgical Products, Inc. · EXPANDER, SURGICAL, SKIN GRAFT41 reports
- N/A 00-7703-030-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft33 reports
- N/A 00-7703-040-00Zimmer Orthopaedic Surgical Products, Inc. · Expander, Surgical, Skin Graft27 reports
- MESHGRAFT™ 00-2195-001-00Zimmer Orthopaedic Surgical Products, Inc. · EXPANDER, SURGICAL, SKIN GRAFT25 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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