Screw, fixation, bone, non-spinal, metallic: medical device reports filed with FDA

1,381 reports carry this product code, 2001–2020; 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.

1,381
reports with this product code: 0% of all MAUDE reports; 0
reports, 12 months to August 2026: 0 in the 12 months before; 1.3%
classified as malfunction: 62.3% across all reports; 0.1%
classified as death, as reported: 0.9% across all reports

Product code NDJ is FDA's classification for "Screw, fixation, bone, non-spinal, metallic" (orthopedic panel), a class 2 device. 1,381 medical device reports carry this product code, 0% of the MAUDE database, from June 2001 to November 2020.

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 injury (98.4%), malfunction (1.3%) and death (0.1%). 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
Pinn Can Bone Screw 6 5mmx25mm	322	32	0%	2.3%
Pinn Can Bone Screw 6 5mmx30mm	294	22	0.3%	3.4%
Pinn Can Bone Screw 6 5mmx20mm	268	19	0.3%	2.4%
Pinn Can Bone Screw 6 5mmx35mm	144	21	0%	6.1%
Pinn Can Bone Screw 6 5mmx15mm	137	16	0.6%	2.7%
Pinn Can Bone Screw 6 5mmx40mm	79	3	0%	4.4%
Apex Hole Elim Positive Stop	1	20	0.4%	13.9%
Pfc Sigmarp Stb Tb In 4 12 5	1	0	0%	0.5%

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
Depuy Orthopaedics US	266	19.3%
Depuy-Raynham A Division Of Depuy Orthopaedics	156	11.3%
Depuy Raynham	98	7.1%
Depuy-Raynham A Div Of Depuy Orthopaedics	79	5.7%
1219655 Depuy-Raynham A Div Of Depuy Orthopaedic	64	4.6%
Depuy Orthopaedics 1818910	27	2%
Depuy Orthopaedic 1818910	4	0.3%
Johnson & Johnson Medical Suzhou	4	0.3%
Raynham	4	0.3%
Depuy Cmw	2	0.1%
Depuy International 8010379	1	0.1%
Depuy Intl 8010379	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

Injury98.4%1,359

Malfunction1.3%18

Other0%0

Not given0.1%2

Who filed

Manufacturer report99.6%1,376

Voluntary report0.3%4

User facility report0%0

Distributor report0%0

Not given0.1%1

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

Device problems coded

Device problem (FDA code)	Reports	Share
Insufficient device problem information	582	42.1%
Loss of osseointegration	367	26.6%
Implant, removal of	115	8.3%
Loose or intermittent connection	97	7%
Osseointegration problem	85	6.2%
Loss of or failure to bond	82	5.9%
Loose	57	4.1%
Malposition of device	46	3.3%
Metal shedding debris	38	2.8%
Breakthe device broke	34	2.5%
Device dislodged or dislocated	28	2%
Migration or expulsion of device	26	1.9%
Fracturea broken bone	18	1.3%
Other (for use when an appropriate device code cannot be identified)	17	1.2%
Explanted	11	0.8%
Noise, audible	10	0.7%
Dislocated	6	0.4%
Replace	6	0.4%
Disassembly	5	0.4%
Inadequacy of device shape and/or size	5	0.4%

Questions about screw, fixation, bone, non-spinal, metallic reports

What is product code NDJ?

FDA's classification code for "Screw, fixation, bone, non-spinal, metallic", class 2, reviewed by the orthopedic panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,381 reports through August 2026, 0 of them in the latest 12 months.

Which brands appear most often?

Pinn Can Bone Screw 6 5mmx25mm (322), Pinn Can Bone Screw 6 5mmx30mm (294), Pinn Can Bone Screw 6 5mmx20mm (268), Pinn Can Bone Screw 6 5mmx35mm (144) and Pinn Can Bone Screw 6 5mmx15mm (137). 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.