DermatomeRecalls & reported problems across all models
Zimmer Orthopaedic Surgical Products, Inc. · 5 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one Dermatome model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1,597
- Deaths reported
- 0
- Injuries reported
- 197
- Recalls
- 2
We found 5 models of Dermatome by Zimmer Orthopaedic Surgical Products, Inc. in the FDA's device registry (GUDID). Together they are named in 1,597 adverse event reports in the FDA's MAUDE database, received between Jul 2, 2019 and Sep 30, 2026 — classified as 197 injuries, 1,400 malfunctions.
The most frequently reported specific device problem is “Failure to Cut” (559 reports).
2 FDA recall records name at least one of these models by its device identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Dermatome recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Nov 24, 2025Open, Classified
The devices may have a misaligned thickness control bar.
Z-0924-2026 · Root cause: Process control · Recall details · FDA record ↗
- Sep 5, 2023Open, Classified
Skin grafts thin and non-uniform when using the affected blades. The issue would be identified at the time of use and may result in the need for additional harvests to adequately cover the area
Z-0069-2024 · Root cause: Process control · Recall details · FDA record ↗
Most reported Dermatome problems
Device problems
- Failure to Cut559
- Unstable234
- Patient Device Interaction Problem182
- Appropriate Device Problem Term/Code Not Available170
- Power Problem128
- Calibration Problem80
- Intermittent Loss of Power79
- Material Deformation69
Patient problems
- No Clinical Signs, Symptoms or Conditions1,253
- Laceration(s)181
- Insufficient Information149
- Skin Tears38
- Abrasion33
- Unspecified Tissue Injury30
- Graft failure18
- No Consequences Or Impact To Patient7
Dermatome models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Dermatome 00-8801-001-00Dermatome1 recall631 reports
- Dermatome 00-8821-001-00Dermatome614 reports
- Dermatome 88710100DERMATOME242 reports
- Dermatome 00-8800-000-10Dermatome1 recall109 reports
- Dermatome 00-8821-006-00Dermatome1 report
Recent Dermatome adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Corroded; Material Deformation; Naturally Worn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950525 ↗MalfunctionSep 28, 2026Calibration Problem
It was reported that outside of surgery, a corrective repair was initiated under a recall after the device was found to cut beyond the intended depth due to a misaligned thickness control bar. There was no patient involvement. During device evaluation, it was discovered that it was missing two Phillips screws. Due diligence is complete; there is no additional information available.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50923818 ↗MalfunctionSep 23, 2026Malposition of Device; Calibration Problem; Material Deformation; Naturally Worn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872921 ↗MalfunctionSep 21, 2026Insufficient Device Problem Information
Patient problems: Insufficient Information
MAUDE report 50840778 ↗MalfunctionSep 18, 2026Corroded; Device Contamination with Chemical or Other Material; Material Deformation; Naturally Worn
It was reported that outside of surgery, the unit had a corroded motor, contaminated insulation and damaged part like plug harness assembly, worn screws and worn reciprocation arm. Inconsistent speed was confirmed after final investigation. There was no patient involvement. Due diligence is complete as no further information is available.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50820425 ↗MalfunctionSep 8, 2026Calibration Problem
It was reported that outside of surgery issue identified during Recall HHE-2025-00141. The issue is related to receiving multiple complaints where the devices were cutting beyond the proper depth due to a misaligned thickness control bar. Proactively carry out maintenance and repair. There was no patient involvement. Upon evaluation it was identified that the widthplate was damaged. Due diligence is complete Attempts have been made and no further information has been provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50666706 ↗MalfunctionSep 1, 2026Mechanical Problem
It was reported that a fault was found at flex during PM. During product evaluation, it was found that width plate was damaged. No patient involvement. Diligence is complete.There was no adverse event associated with this malfunction.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50548002 ↗MalfunctionAug 26, 2026Appropriate Device Problem Term/Code Not Available
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50459174 ↗MalfunctionAug 25, 2026Calibration Problem
It was reported that, outside of surgery, a device issue was identified during a recall in which the device could cut beyond the intended depth due to a misaligned thickness control bar.During device evaluation, it was discovered that the RPMs were unable to be taken due to the reciprocating arm was jumping erratically and would not settle for a reading. There was no patient involvement. Attempts have been made and no further information has been provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437085 ↗MalfunctionAug 25, 2026Appropriate Device Problem Term/Code Not Available
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50435342 ↗MalfunctionAug 21, 2026Calibration Problem
The device was sent in for evaluation due to a recall. There was no patient involvement. During the investigation, it was determined that the motor speeds were out of specification on the low end. Due diligence is complete.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50374762 ↗MalfunctionAug 18, 2026Calibration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50307487 ↗MalfunctionAug 18, 2026Key or Button Unresponsive/not Working
Patient problems: Insufficient Information
MAUDE report 50298989 ↗MalfunctionAug 17, 2026Mechanical Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50283152 ↗MalfunctionAug 14, 2026Appropriate Device Problem Term/Code Not Available
IIt was reported that outside of surgery the unit was sent in for preventative maintenance and later discovered to need repair. Investigation results found device had inconsistent speed. There was no patient involvement. Due diligence is complete.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50252680 ↗
Other Zimmer Orthopaedic Surgical Products, Inc. products
All Zimmer Orthopaedic Surgical Products, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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