Device manufacturer, as written on reports

Becton Dickinson Medical Systems: medical device reports filed with FDA

9,920 reports name it as the manufacturer of the device involved, 2004–2026.

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.

9,920
reports naming it as manufacturer: 0% of all MAUDE reports; 697
reports, 12 months to August 2026: 1,020 in the 12 months before; 96.1%
classified as malfunction: 62.3% across all reports; 0.2%
classified as death, as reported: 0.9% across all reports

9,920 medical device reports received by FDA give Becton Dickinson Medical Systems as the manufacturer of the device involved, 0% of the MAUDE database, from May 2004 to August 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

697 reports arrived in the 12 months to August 2026, down 32% from 1,020 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 (96.1%), injury (3.6%) and death (0.2%). Manufacturers are required to report events they learn of, so a large manufacturer with many products in use files many reports. 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 named most often

Brand	Device type	Reports	Latest 12 months	Classified as death
Bd Safetyglide Needle	Needle, hypodermic, single lumen	1,171	3	0%
BD Luer-Lok	Syringe, piston	696	333	0%
BD SafetyGlide	Needle, hypodermic, single lumen	420	127	0%
Bd Syringe Luer-Lok Tip	Syringe, piston	373	0	0%
Bd Safetyglide Needle Only 25 G	Needle, hypodermic, single lumen	306	0	0%
Bd Integra Syringe With Detachable Needle	Syringe, antistick	252	0	0%
Bd Luer-Lok Syringe	Syringe, piston	220	0	0%
Bd Luer-Lok Tip Syringe	Syringe, piston	189	0	0%
Luer-Lok	Syringe, piston	184	256	0%
Bd Luer-Lok Disposable Syringe With Bd Luer-Lok Tip	Syringe, piston	153	0	0%
Bd Luer-Lok Syringe Bulk Sterile Pharmacy Convenience Tray	Syringe, piston	96	0	0%
3 Ml Bd Luer-Lok Luer-Lok Tip	Syringe, piston	89	0	0%
Syringe 3ml Ll 200 S/C	Syringe, piston	77	0	0%
Bd Plastipak Luer-Lok Syringe	Syringe, piston	33	0	0%
Bd 60ml Syringe Luer-Lok Tip	Syringe, piston	30	0	0%
Bd Plastipak Syringes	Syringe, piston	7	0	0.5%
BD Syringe	Syringe, piston	7	117	0.4%

Brands with a page on this site, 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."

Device types

Product code	Device type	Reports	Share
FMF	Syringe, piston	6,179	62.3%
FMI	Needle, hypodermic, single lumen	2,758	27.8%
MEG	Syringe, antistick	642	6.5%
FOZ	Catheter, intravascular, therapeutic, short-term less than 30 days	130	1.3%
FPA	Set, administration, intravascular	23	0.2%
JKA	Tubes, vials, systems, serum separators, blood collection	20	0.2%
KNT	Tubes, gastrointestinal (and accessories)	14	0.1%
NGT	Saline, vascular access flush	3	0%
DXT	Injector and syringe, angiographic	1	0%
FCM	Tray, catheterization, sterile urethral, with or without catheter (kit)	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

Death0.2%22

Injury3.6%360

Malfunction96.1%9,536

Other0%1

Not given0%1

Grey bar: all 26,136,888 MAUDE reports. Event type is the filer's classification and is not verified by FDA.

Questions about Becton Dickinson Medical Systems reports

How many FDA device reports name Becton Dickinson Medical Systems as manufacturer?

9,920 reports through August 2026, 697 of them in the latest 12 months.

Which of its brands appear most often?

Bd Safetyglide Needle (1,171), BD Luer-Lok (696), BD SafetyGlide (420), Bd Syringe Luer-Lok Tip (373) and Bd Safetyglide Needle Only 25 G (306).

Which device types does it report on?

syringe, piston (62.3%), needle, hypodermic, single lumen (27.8%), syringe, antistick (6.5%) and catheter, intravascular, therapeutic, short-term less than 30 days (1.3%).

Does a high count say something about the manufacturer?

Not by itself. Manufacturers must file a report for every event they become aware of, so report volume follows the number of devices in use. 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."

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. Manufacturer names are pooled after company suffixes (Inc., LLC, GmbH and similar) are dropped; names that read as a person rather than an organisation are never published. 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.