Devices › Endoscopic grasping/cutting instrument, non-powered

Device brand name · Endoscopic grasping/cutting instrument non-powered

Pkg 5mm Peek Monopolar Handle: medical device reports filed with FDA

406 reports name it, 2016–2018. Manufacturer given most often on reports: Stryker Endoscopy-San Jose. Product code OCZ.

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.

406
device reports naming the brand: 0% of all MAUDE reports · about 42 a year; 0
reports, 12 months to August 2026: 0 in the 12 months before; 100%
classified as malfunction: 96.2% across the product code; 0%
classified as death, as reported: 0 reports · not verified by FDA

406 medical device reports received by FDA name the brand "Pkg 5mm Peek Monopolar Handle" (endoscopic grasping/cutting instrument non-powered); the manufacturer given most often on reports is Stryker Endoscopy-San Jose; received from October 2016 to May 2018. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.

0 reports arrived in the 12 months to August 2026, and none in 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 (100%); across all endoscopic grasping/cutting instrument, non-powered reports (product code OCZ) death is recorded in 0% and malfunction in 96.2%. Event type is the reporter's classification of the report, not a verified outcome.

The device problems coded most often are device operates differently than expected (42.6%), device packaging compromised (35%) and break (17.7%). The patient problems coded most often are no patient involvement. 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."

Reports by month, five years

No report naming Pkg 5mm Peek Monopolar Handle was received in the five years to August 2026; the latest was received in May 2018.

By year received

Event type and report source

Event type, as classified on the report

Death0%0

Injury0%0

Malfunction100%406

Other0%0

Not given0%0

Who filed the report

Manufacturer report100%406

Voluntary report0%0

User facility report0%0

Distributor report0%0

Not given0%0

Grey bar: all 2,212 reports carrying product code OCZ. Event type is the filer's classification and is not verified by FDA.

Device problems coded

Device problem (FDA code)	Reports	Share	Share across product code
Device operates differently than expectedthe device behaved unexpectedly	173	42.6%	30.5%
Device packaging compromised	142	35%	25.9%
Breakthe device broke	72	17.7%	25.1%
Material integrity problema problem with the device material	12	3%	3.5%
Arcing	2	0.5%	0.4%
Device inoperablethe device could not be used	2	0.5%	0.3%
Bent	1	0.2%	0.1%
Defective component	1	0.2%	0.1%
Failure of device to self-test	1	0.2%	0.1%

FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.

Patient problems coded

Patient problem (FDA code)	Reports	Share
No patient involvement	12	3%

Patient problem codes are present mainly in reports filed since 2019 and are often blank.

In context

Measure	Pkg 5mm Peek Monopolar Handle	Product code OCZ	All MAUDE reports
Reports	406	2,212	26,136,888
Share of that pool	—	18.4%	0%
Classified as death, per 1,000 reports	0	0	9
Classified as injury	0%	3.6%	36.2%
Classified as malfunction	100%	96.2%	62.3%
Filed by the manufacturer	100%	97.4%	94.9%

Shares are of reports, not of devices in use. 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."

Other brands with product code OCZ

Brand	Reports	Classified as death
5mm 33cm Peek Monopolar Handle 33cm	927	0%
5mm Peek Multifunction Handle	394	0%
5mm Monopolar Handle 33cm	304	0%
5mm Ratcheted Handle 33cm	236	0%
10mm 33cm Peek Monopolar Handle	219	0%

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." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."

Questions about Pkg 5mm Peek Monopolar Handle reports

How many FDA reports name Pkg 5mm Peek Monopolar Handle?

406 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.

What kinds of events are reported?

malfunction (100%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.

What device problems are coded?

device operates differently than expected (42.6%), device packaging compromised (35%), break (17.7%), material integrity problem (3%) and arcing (0.5%). These are FDA's device problem codes as entered on the report.

Who files these reports?

manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.

Do these reports show that Pkg 5mm Peek Monopolar Handle was at fault?

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." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."

How do I report a problem with a medical device?

Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.

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. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. 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.