Syringe, antistick: medical device reports filed with FDA

2,952 reports carry this product code, 2000–2026; 12 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.

2,952
reports with this product code: 0% of all MAUDE reports; 96
reports, 12 months to August 2026: 177 in the 12 months before; 88.1%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

Product code MEG is FDA's classification for "Syringe, antistick" (general Hospital panel), a class 2 device. 2,952 medical device reports carry this product code, 0% of the MAUDE database, from February 2000 to August 2026.

96 reports arrived in the 12 months to August 2026, down 46% from 177 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 (88.1%), injury (8.7%) and other (2%). 12 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
Bd Integra Syringe With Detachable Needle	247	0	0%	83.1%
VanishPoint	153	9	0%	95.7%
Sol-Millennium	56	5	0%	100%
BD SafetyGlide	42	127	0%	98.4%
Bd Insulin Syringe With The Bd Ultra-Fine Needle	6	0	0%	97.5%
Jelco	4	34	0%	84.3%
Monoject	3	14	0.2%	88.4%
Bd Precisionglide Needle	2	0	0%	95.9%
Magellan	2	20	0%	95.2%
Portex	2	8	0.6%	80.6%
Bd Insulin Syringes With Bd Ultra-Fine Needle	1	0	0%	99.2%
Spectrum Infusion Pump	1	15	0%	99.7%

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
Becton Dickinson Medical Systems	642	21.7%
Bd Medical - Diabetes Care	286	9.7%
Becton Dickinson	67	2.3%
Bd Medical Bd West Medical Surgical	33	1.1%
Bd	19	0.6%
Becton Dickinson And	19	0.6%
Terumo Medical	8	0.3%
Smiths Medical	6	0.2%
Mhc Medical Products	4	0.1%
Becton Dickinson Ind Cirurgicas Ltda	2	0.1%
Becton Dickinson Infusion Therapy Systems	2	0.1%
Becton Dickinson & Bd	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%0

Injury8.7%258

Malfunction88.1%2,600

Other2%58

Not given1.2%36

Who filed

Manufacturer report80.6%2,380

Voluntary report11.1%329

User facility report0%0

Distributor report0%1

Not given8.2%242

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

Device problems coded

Device problem (FDA code)	Reports	Share
Leak/splashthe device leaked	521	17.6%
Breakthe device broke	387	13.1%
Difficult or delayed activation	352	11.9%
Retraction problem	314	10.6%
Fluid/blood leak	114	3.9%
Detachment of device component	101	3.4%
Detachment of device or device componentpart of the device came off	93	3.2%
Fail-safe problem	90	3%
Device contamination with chemical or other material	75	2.5%
Failure to deliverthe device did not deliver the dose or item	68	2.3%
Activation problem	67	2.3%
Defective devicethe device was defective	66	2.2%
Activation failure	56	1.9%
Device operates differently than expectedthe device behaved unexpectedly	54	1.8%
Defective component	50	1.7%
Device contaminated during manufacture or shipping	46	1.6%
Material protrusion/extrusion	46	1.6%
Device markings/labelling problema problem with the device markings or label	37	1.3%
Material twisted/bent	35	1.2%
Bent	34	1.2%

Questions about syringe, antistick reports

What is product code MEG?

FDA's classification code for "Syringe, antistick", class 2, reviewed by the general Hospital panel. Every device report carries the product code of the device involved.

How many reports carry this code?

2,952 reports through August 2026, 96 of them in the latest 12 months.

Which brands appear most often?

Bd Integra Syringe With Detachable Needle (247), VanishPoint (153), Sol-Millennium (56), BD SafetyGlide (42) and Bd Insulin Syringe With The Bd Ultra-Fine Needle (6). 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.