Expander, surgical, skin graft: medical device reports filed with FDA

5,270 reports carry this product code, 1992–2026; 9 brands with a page.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

5,270
reports with this product code: 0% of all MAUDE reports; 419
reports, 12 months to August 2026: 454 in the 12 months before; 94.9%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

Product code FZW is FDA's classification for "Expander, surgical, skin graft" (general, Plastic Surgery panel), a class 1 device. 5,270 medical device reports carry this product code, 0% of the MAUDE database, from July 1992 to August 2026.

419 reports arrived in the 12 months to August 2026, close to the 454 of the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (94.9%) and injury (5%). 9 brand names with a page on this site carry this code; the brands table is ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction
Zimmer Skin Graft Mesher	3,285	285	0%	96%
Z S G M Cutter 1 5 1 Ratio Caution Sharp	339	17	0%	99.7%
Z S G M Cutter 2 1 Ratio Caution Sharp	217	6	0%	99.5%
Padgett Model S Slimline Electric Dermatome	49	0	0%	75.7%
Zimmer Air Dermatome	5	372	0%	79.6%
Air Dermatome Handpiece	3	0	0%	67.3%
Dermatome AN Handpiece	1	117	0%	87.2%
Fan Spray Kit	1	173	0%	98.2%
Handpiece Electric Dermatome	1	174	0%	92.6%

Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Zimmer Surgical	5,012	95.1%
Integra Lifesciences Oh/USA	47	0.9%
Integra Lifesciences	16	0.3%
Smith & Nephew Medical	7	0.1%
Mcghan Medical	6	0.1%
Hill-Rom	1	0%
Mentor	1	0%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type and report source

Event type

Death0%0

Injury5%266

Malfunction94.9%5,000

Other0%2

Not given0%2

Who filed

Manufacturer report99.4%5,241

Voluntary report0.2%9

User facility report0%0

Distributor report0%1

Not given0.4%19

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Failure to cut	2,311	43.9%
Material twisted/bent	961	18.2%
Physical resistance/sticking	531	10.1%
Device operates differently than expectedthe device behaved unexpectedly	343	6.5%
Bent	228	4.3%
Breakthe device broke	138	2.6%
Material deformation	137	2.6%
Mechanical jam	122	2.3%
Mechanical problema mechanical problem	117	2.2%
Naturally worn	98	1.9%
Retraction problem	90	1.7%
Failure to advance	80	1.5%
Fitting problem	76	1.4%
Insufficient device problem information	71	1.3%
Patient device interaction problem	60	1.1%
Component missing	58	1.1%
Difficult to removethe device was hard to remove	57	1.1%
Dull, blunt	47	0.9%
Calibration problem	44	0.8%
Delivered as unsterile product	41	0.8%

Questions about expander, surgical, skin graft reports

What is product code FZW?

FDA's classification code for "Expander, surgical, skin graft", class 1, reviewed by the general, Plastic Surgery panel. Every device report carries the product code of the device involved.

How many reports carry this code?

5,270 reports through August 2026, 419 of them in the latest 12 months.

Which brands appear most often?

Zimmer Skin Graft Mesher (3,285), Z S G M Cutter 1 5 1 Ratio Caution Sharp (339), Z S G M Cutter 2 1 Ratio Caution Sharp (217), Padgett Model S Slimline Electric Dermatome (49) and Zimmer Air Dermatome (5). Widely used products collect more reports because more people use them.

Can the brands table be used to rank the devices?

No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." Brands differ in how many are in use, how long they have been sold and how reports are collected.

Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.