Tap, bone: medical device reports filed with FDA

1,316 reports carry this product code, 1992–2026; 8 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.

1,316
reports with this product code: 0% of all MAUDE reports; 163
reports, 12 months to August 2026: 95 in the 12 months before; 86.9%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

Product code HWX is FDA's classification for "Tap, bone" (orthopedic panel), a class 1 device. 1,316 medical device reports carry this product code, 0% of the MAUDE database, from June 1992 to August 2026.

163 reports arrived in the 12 months to August 2026, up 72% from 95 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 (86.9%), injury (11.9%) and other (0.8%). 8 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
Handle With Quick Coupling Small	217	16	0%	99.6%
Manual Orthopedic Surgical Instrument	68	0	0.1%	88%
Invictus	8	0	0%	74.3%
Orthopedic Manual Surgical Instrument	3	0	0.2%	85.9%
Level One	2	31	1.7%	45.9%
Depth Gauge For 2 0mm And 2 4mm Screws	1	68	0%	100%
T-Handle	1	17	0%	90.2%
Unk Reamer	1	71	0%	96.3%

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
Alphatec Spine	77	5.9%
Medos International S Rl Ch	38	2.9%
Stryker Spine Bordeaux	30	2.3%
Depuy Spine	21	1.6%
Medtronic Sofamor Danek	14	1.1%
Biomet Microfixation	13	1%
Synthes Brandywine	11	0.8%
Abbott Spine	10	0.8%
Medtronic Sofamor Danek USA	10	0.8%
Warsaw Orthopedic	7	0.5%
Warsaw Orthopedics	6	0.5%
Linvatec	4	0.3%
Synthes	4	0.3%
Synthes USA	4	0.3%
Zimmer Spine	3	0.2%

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

Injury11.9%157

Malfunction86.9%1,143

Other0.8%11

Not given0.4%5

Who filed

Manufacturer report98.1%1,291

Voluntary report1.3%17

User facility report0%0

Distributor report0.2%2

Not given0.5%6

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

Device problems coded

Device problem (FDA code)	Reports	Share
Breakthe device broke	699	53.1%
Device-device incompatibility	212	16.1%
Fracturea broken bone	80	6.1%
Contamination /decontamination problem	72	5.5%
Material deformation	47	3.6%
Detachment of device component	31	2.4%
Material fragmentation	28	2.1%
Failure to cut	24	1.8%
Crackthe device cracked	19	1.4%
Entrapment of device	19	1.4%
Device, or device fragments remain in patient	17	1.3%
Difficult to removethe device was hard to remove	17	1.3%
Material separation	16	1.2%
Tip breakage	15	1.1%
Device operates differently than expectedthe device behaved unexpectedly	14	1.1%
Mechanical jam	14	1.1%
Detachment of device or device componentpart of the device came off	12	0.9%
Bent	10	0.8%
Corrodedthe device corroded	9	0.7%
Failure to adhere or bond	9	0.7%

Questions about tap, bone reports

What is product code HWX?

FDA's classification code for "Tap, bone", class 1, reviewed by the orthopedic panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,316 reports through August 2026, 163 of them in the latest 12 months.

Which brands appear most often?

Handle With Quick Coupling Small (217), Manual Orthopedic Surgical Instrument (68), Invictus (8), Orthopedic Manual Surgical Instrument (3) and Level One (2). 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.