Prosthesis, elbow, constrained, cemented: medical device reports filed with FDA

3,077 reports carry this product code, 1992–2026; 4 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.

3,077
reports with this product code: 0% of all MAUDE reports; 180
reports, 12 months to August 2026: 219 in the 12 months before; 6.4%
classified as malfunction: 62.3% across all reports; 0.4%
classified as death, as reported: 0.9% across all reports

Product code JDC is FDA's classification for "Prosthesis, elbow, constrained, cemented" (orthopedic panel), a class 2 device. 3,077 medical device reports carry this product code, 0% of the MAUDE database, from July 1992 to August 2026.

180 reports arrived in the 12 months to August 2026, down 18% from 219 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 (92.9%), malfunction (6.4%) and death (0.4%). 4 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
Discovery Elbow	444	0	0%	1.1%
Unknown Humeral Stem	15	15	1.2%	0.6%
Unknown Extremity	12	0	1.9%	1.9%
Unk Liner	1	121	0%	3.2%

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
Encore Medical L P	760	24.7%
Zimmer	513	16.7%
Biomet Orthopedics	92	3%
Tornier	73	2.4%
Biomet	37	1.2%
Limacorporate	25	0.8%
Stanmore Implants Worldwide	15	0.5%
Biomet UK	10	0.3%
Dow Corning	2	0.1%
Sulzer Orthopedics	2	0.1%
Acumed	1	0%
Zimmer Biomet	1	0%

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

Death0.4%13

Injury92.9%2,860

Malfunction6.4%198

Other0.1%4

Not given0.1%2

Who filed

Manufacturer report99%3,045

Voluntary report0.5%15

User facility report0%0

Distributor report0.1%4

Not given0.4%13

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

Device problems coded

Device problem (FDA code)	Reports	Share
Insufficient device problem information	510	16.6%
Fracturea broken bone	280	9.1%
Explanted	210	6.8%
Loosening of implant not related to bone-ingrowth	204	6.6%
Loose or intermittent connection	183	5.9%
Naturally worn	145	4.7%
Migration or expulsion of device	138	4.5%
Device dislodged or dislocated	115	3.7%
Breakthe device broke	101	3.3%
Device slipped	81	2.6%
Failure to adhere or bond	80	2.6%
Loose	76	2.5%
Unstable	71	2.3%
Implant, removal of	68	2.2%
Component(s), worn	65	2.1%
Replace	55	1.8%
Disassembly	45	1.5%
Detachment of device or device componentpart of the device came off	38	1.2%
Migrationthe device moved from where it was placed	32	1%
Patient device interaction problem	27	0.9%

Questions about prosthesis, elbow, constrained, cemented reports

What is product code JDC?

FDA's classification code for "Prosthesis, elbow, constrained, cemented", class 2, reviewed by the orthopedic panel. Every device report carries the product code of the device involved.

How many reports carry this code?

3,077 reports through August 2026, 180 of them in the latest 12 months.

Which brands appear most often?

Discovery Elbow (444), Unknown Humeral Stem (15), Unknown Extremity (12) and Unk Liner (1). 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.