Washer, bolt nut: medical device reports filed with FDA

1,514 reports carry this product code, 1992–2026; 2 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.

1,514
reports with this product code: 0% of all MAUDE reports; 215
reports, 12 months to August 2026: 185 in the 12 months before; 51.9%
classified as malfunction: 62.3% across all reports; 0.1%
classified as death, as reported: 0.9% across all reports

Product code HTN is FDA's classification for "Washer, bolt nut" (orthopedic panel), a class 2 device. 1,514 medical device reports carry this product code, 0% of the MAUDE database, from December 1992 to August 2026.

215 reports arrived in the 12 months to August 2026, up 16% from 185 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 (51.9%), injury (46.4%) and other (1.3%). 2 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
Unknown Knee Femoral Adaptor Bolt	3	8	0%	3.6%
Unk - Nail Head Elements Fns Bolt	2	12	0%	8.1%

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
Arthrex	143	9.4%
Acumed	39	2.6%
Smith & Nephew Endoscopy Division	6	0.4%
Biomet Microfixation	3	0.2%
Synthes	3	0.2%
Conmed Linvatec	2	0.1%
Stryker Trauma Kiel	2	0.1%
Synthes USA	1	0.1%
Wright Medical Technology	1	0.1%

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

Death0.1%2

Injury46.4%703

Malfunction51.9%786

Other1.3%20

Not given0.2%3

Who filed

Manufacturer report97.8%1,481

Voluntary report1%15

User facility report0%0

Distributor report0.3%4

Not given0.9%14

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

Device problems coded

Device problem (FDA code)	Reports	Share
Breakthe device broke	487	32.2%
Device-device incompatibility	83	5.5%
Detachment of device or device componentpart of the device came off	64	4.2%
Insufficient device problem information	61	4%
Material split, cut or torn	51	3.4%
Device dislodged or dislocated	47	3.1%
Patient device interaction problem	47	3.1%
Positioning failure	44	2.9%
Device slipped	37	2.4%
Explanted	35	2.3%
Difficult to advance	27	1.8%
Migrationthe device moved from where it was placed	26	1.7%
Entrapment of device	22	1.5%
Device operates differently than expectedthe device behaved unexpectedly	20	1.3%
Fracturea broken bone	20	1.3%
Physical resistance/sticking	20	1.3%
Defective devicethe device was defective	18	1.2%
Failure to advance	16	1.1%
Migration or expulsion of device	15	1%
Detachment of device component	11	0.7%

Questions about washer, bolt nut reports

What is product code HTN?

FDA's classification code for "Washer, bolt nut", class 2, reviewed by the orthopedic panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,514 reports through August 2026, 215 of them in the latest 12 months.

Which brands appear most often?

Unknown Knee Femoral Adaptor Bolt (3) and Unk - Nail Head Elements Fns Bolt (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.