Acid, hyaluronic, intraarticular: medical device reports filed with FDA

8,423 reports carry this product code, 1997–2026; 11 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.

8,423
reports with this product code: 0% of all MAUDE reports; 139
reports, 12 months to August 2026: 245 in the 12 months before; 8.1%
classified as malfunction: 62.3% across all reports; 3.7%
classified as death, as reported: 0.9% across all reports

Product code MOZ is FDA's classification for "Acid, hyaluronic, intraarticular" (unknown panel), a class 3 device. 8,423 medical device reports carry this product code, 0% of the MAUDE database, from July 1997 to August 2026.

139 reports arrived in the 12 months to August 2026, down 43% from 245 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 (66.3%), other (17.1%) and malfunction (8.1%). 11 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
Synvisc One	1,916	13	1.4%	26.5%
Synvisc	1,389	12	1.6%	0.6%
Synvisc Hylan G-F 20 Injection	1,154	0	0.2%	0%
Euflexxa	670	26	18.2%	0.3%
Synvisc One Hylan G-F 20 Injection	400	0	0.3%	0%
Orthovisc	259	4	6.8%	9.8%
Hyalgan	258	0	3%	0.4%
Synvisc One Synvisc One	222	0	1.8%	0%
Synvisc Synvisc	185	0	1.1%	0%
Hydrelle	2	0	0%	0.6%
Restylane	1	6	0%	1.8%

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
Genzyme Biosurgery Ridgefield	3,295	39.1%
Genzyme Ridgefield	1,052	12.5%
Q-Med	32	0.4%
Lifecore Biomedical	4	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

Death3.7%310

Injury66.3%5,588

Malfunction8.1%679

Other17.1%1,439

Not given4.8%407

Who filed

Manufacturer report77.6%6,539

Voluntary report18.2%1,533

User facility report0%0

Distributor report4%335

Not given0.2%16

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

Device problems coded

Device problem (FDA code)	Reports	Share
Insufficient device problem information	1,980	23.5%
Patient-device incompatibilitythe device did not suit the patient	772	9.2%
Device contamination with biological material	536	6.4%
Device operates differently than expectedthe device behaved unexpectedly	242	2.9%
Device remains implanted	219	2.6%
Microbial contamination of device	179	2.1%
Reactiona reaction, type not specified	146	1.7%
Off-label use	119	1.4%
Nonstandard device	98	1.2%
Improper or incorrect procedure or method	73	0.9%
Breakthe device broke	47	0.6%
Patient device interaction problem	41	0.5%
Therapeutic or diagnostic output failure	41	0.5%
Unexpected therapeutic results	22	0.3%
Contamination	20	0.2%
Other (for use when an appropriate device code cannot be identified)	18	0.2%
Leak/splashthe device leaked	10	0.1%
Manufacturing, packaging or shipping problem	10	0.1%
Detachment of device or device componentpart of the device came off	8	0.1%
Lack of effect	8	0.1%

Questions about acid, hyaluronic, intraarticular reports

What is product code MOZ?

FDA's classification code for "Acid, hyaluronic, intraarticular", class 3, reviewed by the unknown panel. Every device report carries the product code of the device involved.

How many reports carry this code?

8,423 reports through August 2026, 139 of them in the latest 12 months.

Which brands appear most often?

Synvisc One (1,916), Synvisc (1,389), Synvisc Hylan G-F 20 Injection (1,154), Euflexxa (670) and Synvisc One Hylan G-F 20 Injection (400). 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.