Device manufacturer, as written on reports
Becton Dickinson And: medical device reports filed with FDA
11,336 reports name it as the manufacturer of the device involved, 1992–2026.
- 11,336
- reports naming it as manufacturer
- 0% of all MAUDE reports
- 333
- reports, 12 months to August 2026
- 441 in the 12 months before
- 92%
- classified as malfunction
- 62.3% across all reports
- 0.1%
- classified as death, as reported
- 0.9% across all reports
11,336 medical device reports received by FDA give Becton Dickinson And as the manufacturer of the device involved, 0% of the MAUDE database, from April 1992 to August 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.
333 reports arrived in the 12 months to August 2026, down 24% from 441 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 (92%), injury (6.7%) and other (0.7%). 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 Nano 2nd Gen Pen Needle | Needle, hypodermic, single lumen | 712 | 0 | 0% |
| Bd Ultra Fine Pen Needles | Needle, hypodermic, single lumen | 610 | 0 | 0% |
| Bd Ultra Fine Pen Needle | Needle, hypodermic, single lumen | 339 | 0 | 0% |
| Bd Ultra-Fine Pen Needle | Needle, hypodermic, single lumen | 267 | 0 | 0% |
| BD Insyte Autoguard | Catheter, intravascular, therapeutic, short-term less than 30 days | 229 | 55 | 0% |
| Bd Ultra-Fine Nano Pen Needles 4mm 5/32 32g | Needle, hypodermic, single lumen | 217 | 0 | 0% |
| Pen Ndl 32g 4mm Hp 100 Box 1200 Us | Needle, hypodermic, single lumen | 205 | 0 | 0% |
| Bd Nano 2nd Gen Pen Needles 32g X 4mm 100 Count | Needle, hypodermic, single lumen | 183 | 0 | 0% |
| Bd Autoshield Duo Safety Pen Needle | Needle, hypodermic, single lumen | 180 | 0 | 0% |
| Bd Micro-Fine Pro Pen Needle | Needle, hypodermic, single lumen | 166 | 0 | 0% |
| Bd Ultra-Fine Pro Pen Needle | Needle, hypodermic, single lumen | 142 | 0 | 0% |
| Bd Autoshield Duo Pen Needle | Needle, hypodermic, single lumen | 128 | 0 | 0% |
| Pen Ndl 32g 4mm 100bx 1200 Usa | Needle, hypodermic, single lumen | 113 | 10 | 0% |
| BD Luer-Lok | Syringe, piston | 83 | 333 | 0% |
| Pen Ndl 32g 4mm Pro 14 Bag 700 Case Jpx | Needle, hypodermic, single lumen | 78 | 19 | 0% |
| Bd Precisionglide Needle | Needle, hypodermic, single lumen | 51 | 0 | 0% |
| Bd Micro-Fine + Pen Needle | Needle, hypodermic, single lumen | 47 | 0 | 0% |
| BD Nexiva | Catheter, intravascular, therapeutic, short-term less than 30 days | 47 | 14 | 0% |
| Bd 60ml Syringe Luer-Lok Tip | Syringe, piston | 34 | 0 | 0% |
| 10 Ml Bd Posiflush Normal Saline Syringe | Saline, vascular access flush | 32 | 0 | 0% |
| Insyte AUTOGUARD | Catheter, intravascular, therapeutic, short-term less than 30 days | 24 | 1,050 | 0% |
| BD Vacutainer Push Button Blood Collection Set | Tubes, vials, systems, serum separators, blood collection | 18 | 324 | 0% |
| Bd | Syringe, piston | 15 | 0 | 1% |
| BD alaris pump infusion set | Set, administration, intravascular | 10 | 55 | 1.1% |
| Nexiva | Catheter, intravascular, therapeutic, short-term less than 30 days | 9 | 304 | 0% |
| BD Vacutainer Eclipse Blood Collection Needle | Needle, hypodermic, single lumen | 8 | 627 | 0% |
| BD Vacutainer Buffered Sodium Citrate (9NC) Blood Collection Tubes | Tubes, vials, systems, serum separators, blood collection | 7 | 211 | 0% |
| BD SafetyGlide | Needle, hypodermic, single lumen | 5 | 127 | 0% |
| BD Vacutainer Safety-Lok Blood Collection Set | Tubes, vials, systems, serum separators, blood collection | 5 | 144 | 0% |
| BD Vacutainer UltraTouch Push Button Blood Collection Set | Set, administration, intravascular | 5 | 581 | 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 |
|---|---|---|---|
| FMI | Needle, hypodermic, single lumen | 8,525 | 75.2% |
| FMF | Syringe, piston | 778 | 6.9% |
| FOZ | Catheter, intravascular, therapeutic, short-term less than 30 days | 751 | 6.6% |
| NGT | Saline, vascular access flush | 510 | 4.5% |
| JKA | Tubes, vials, systems, serum separators, blood collection | 227 | 2% |
| FPA | Set, administration, intravascular | 214 | 1.9% |
| GAA | Needle, aspiration and injection, disposable | 64 | 0.6% |
| FRN | Pump, infusion | 53 | 0.5% |
| NSC | Injector, pen | 37 | 0.3% |
| MEG | Syringe, antistick | 19 | 0.2% |
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
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 And reports
How many FDA device reports name Becton Dickinson And as manufacturer?
11,336 reports through August 2026, 333 of them in the latest 12 months.
Which of its brands appear most often?
Bd Nano 2nd Gen Pen Needle (712), Bd Ultra Fine Pen Needles (610), Bd Ultra Fine Pen Needle (339), Bd Ultra-Fine Pen Needle (267) and BD Insyte Autoguard (229).
Which device types does it report on?
needle, hypodermic, single lumen (75.2%), syringe, piston (6.9%), catheter, intravascular, therapeutic, short-term less than 30 days (6.6%) and saline, vascular access flush (4.5%).
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.