Remb Handswitch: medical device reports filed with FDA

150 reports name it, 2015–2016. Manufacturer given most often on reports: Stryker Instruments-Kalamazoo. Product code ERL.

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.

150
device reports naming the brand: 0% of all MAUDE reports · about 13 a year; 0
reports, 12 months to August 2026: 0 in the 12 months before; 100%
classified as malfunction: 98.9% across the product code; 0%
classified as death, as reported: 0 reports · not verified by FDA

FDA's MAUDE database holds 150 reports that name the brand "Remb Handswitch" (drill surgical ent electric or pneumatic including handpiece), received between January 2015 and July 2016; the manufacturer given most often on reports is Stryker Instruments-Kalamazoo. Spellings of one product vary from report to report.

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 drill, surgical, ent (electric or pneumatic) including handpiece reports (product code ERL) death is recorded in 0% and malfunction in 98.9%. Event type is the reporter's classification of the report, not a verified outcome.

The device problems coded most often are positioning problem (48%), detachment of device or device component (26%) and device markings/labelling problem (20%). 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 Remb Handswitch was received in the five years to August 2026; the latest was received in July 2016.

Event type and report source

Event type, as classified on the report

Death0%0

Injury0%0

Malfunction100%150

Other0%0

Not given0%0

Who filed the report

Manufacturer report100%150

Voluntary report0%0

User facility report0%0

Distributor report0%0

Not given0%0

Grey bar: all 29,931 reports carrying product code ERL. 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
Positioning problem	72	48%	0.4%
Detachment of device or device componentpart of the device came off	39	26%	4%
Device markings/labelling problema problem with the device markings or label	30	20%	0.3%
Unintended power up	5	3.3%	2.5%
Breakthe device broke	2	1.3%	5.2%
Disassembly	1	0.7%	0.6%

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	138	92%

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

In context

Measure	Remb Handswitch	Product code ERL	All MAUDE reports
Reports	150	29,931	26,136,888
Share of that pool	—	0.5%	0%
Classified as death, per 1,000 reports	0	0	9
Classified as injury	0%	0.9%	36.2%
Classified as malfunction	100%	98.9%	62.3%
Filed by the manufacturer	100%	99.5%	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 ERL

Brand	Reports	Latest 12 months	Classified as death
Xmax Motor	4,447	0	0%
Remb Electric Sagittal Saw	1,693	4	0%
Core Impaction Drill	3,913	0	0%
S2 Drill	844	79	0%
Motor Assembly Xmax	893	14	0%
Ipc Handpiece - Xps Straightshot M5	711	124	0%
Remb Electric Micro Drill	660	9	0%
Xps Handpiece - Visao	649	12	0%
Ipc Handpiece - Xps Straightshot M4	607	45	0%
Pi Drive Plus Motor	564	0	0%
Micro Sagittal Saw	1,395	0	0%
Core Universal Driver	679	0	0%
ENT Mr8	622	538	0%
Pi Drive Motor	477	0	0%
Core Sumex Drill	522	0	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 Remb Handswitch reports

How many FDA reports name Remb Handswitch?

150 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?

positioning problem (48%), detachment of device or device component (26%), device markings/labelling problem (20%), unintended power up (3.3%) and break (1.3%). 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 Remb Handswitch 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.