Device manufacturer, as written on reports

Becton Dickinson De Mexico: medical device reports filed with FDA

1,212 reports name it as the manufacturer of the device involved, 2017–2026.

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.

1,212
reports naming it as manufacturer: 0% of all MAUDE reports; 92
reports, 12 months to August 2026: 130 in the 12 months before; 98.9%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

1,212 medical device reports received by FDA give Becton Dickinson De Mexico as the manufacturer of the device involved, 0% of the MAUDE database, from August 2017 to August 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

92 reports arrived in the 12 months to August 2026, down 29% from 130 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 (98.9%) and injury (1.1%). 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 Luer-Lok Disposable Syringe With Bd Luer-Lok Tip	Syringe, piston	107	0	0%
BD Luer-Lok	Syringe, piston	94	333	0%
3 Ml Bd Luer-Lok Luer-Lok Tip	Syringe, piston	83	0	0%
Bd Plastipak Syringe	Syringe, piston	56	25	0%
Syringe 3ml Ll 200 S/C	Syringe, piston	52	0	0%
Bd Luer-Lok Tip Syringe	Syringe, piston	29	0	0%
Bd Ultra-Fine Insulin Syringe	Syringe, piston	23	0	0%
Bd Plastipak Luer-Lok Syringe	Syringe, piston	15	0	0%
Bd Luer-Lok Syringe	Syringe, piston	12	0	0%
Bd 60ml Syringe Luer-Lok Tip	Syringe, piston	11	0	0%
Bd Precisionglide Needle	Needle, hypodermic, single lumen	11	0	0%
Bd Syringe With Needle	Syringe, piston	9	0	0%
Bd Plastipak Syringes	Syringe, piston	6	0	0.5%
Bd Syringe Luer-Lok Tip	Syringe, piston	6	0	0%
BD Syringe	Syringe, piston	4	117	0.4%
Luer-Lok	Syringe, piston	4	256	0%
Bd Ultra-Fine Pen Needle	Needle, hypodermic, single lumen	2	0	0%
Bd Microtainer Contact-Activated Lancet	Single use only blood lancet with an integral sharps injury prevention feature	1	10	0%
Bd Nano 2nd Gen Pen Needle	Needle, hypodermic, single lumen	1	0	0%

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	1,084	89.4%
FMI	Needle, hypodermic, single lumen	91	7.5%
GAA	Needle, aspiration and injection, disposable	10	0.8%
JSG	Culture media, non-selective and non-differential	7	0.6%
JSJ	Culture media, selective and non-differential	6	0.5%
NGT	Saline, vascular access flush	2	0.2%
FMK	Single use only blood lancet with an integral sharps injury prevention feature	1	0.1%
FPA	Set, administration, intravascular	1	0.1%
JKA	Tubes, vials, systems, serum separators, blood collection	1	0.1%
JQP	Calculator/data processing module, for clinical use	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

Death0%0

Injury1.1%13

Malfunction98.9%1,199

Other0%0

Not given0%0

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 De Mexico reports

How many FDA device reports name Becton Dickinson De Mexico as manufacturer?

1,212 reports through August 2026, 92 of them in the latest 12 months.

Which of its brands appear most often?

Bd Luer-Lok Disposable Syringe With Bd Luer-Lok Tip (107), BD Luer-Lok (94), 3 Ml Bd Luer-Lok Luer-Lok Tip (83), Bd Plastipak Syringe (56) and Syringe 3ml Ll 200 S/C (52).

Which device types does it report on?

syringe, piston (89.4%), needle, hypodermic, single lumen (7.5%), needle, aspiration and injection, disposable (0.8%) and culture media, non-selective and non-differential (0.6%).

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.