2026 data FDA MAUDE openFDA FDA Class II

Syringe, Antistick

Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.

OpenFDA device adverse-event casebook.

FDA Class II (moderate risk, special controls required), regulated under 21 CFR §880.5860 (General Hospital panel).

FDA MAUDE casebook

openFDA event book Syringe, Antistick LIGHT-BOOK · MAUDE

#414 of 1000 · 2,941 reports · 2000–2026

  • BOOK 2,941 reports
  • RANK #414 of 1000
  • DEATH 0 death-typed
  • INJ 257 injury-typed
  • MALF 2,592 malfunction
  • SPAN 2000–2026
  • PEAK 2021: 541
  • PHOTO Assay

Nearest event-volume peer: Assay, Glycosylated Hemoglobin (2 report gap)

Syringe, Antistick sits #414 of 1000 among tracked device types with 2,941 MAUDE reports spanning 2000–2026. Rank counts report volume, not confirmed device fault. Event_type Death / Injury / Malfunction are one code per report — not the same population as patient-outcome rows ( methodology). Read with this device → · Lead manufacturer → · Similar-volume device →

Malfunction reports run above the device-type norm

Syringe, Antistick carries 88.1% MALFUNCTION-coded reports, 23.3pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.

  • DEATH 0.0% corpus 1.5% · below corpus mean (-1.5 pp)
  • INJ 8.7% corpus 30.3% · below corpus mean (-21.6 pp)
  • MALF 88.1% corpus 64.8% · above corpus mean (+23.3 pp)

Lead product-problem code Leak/Splash is 19% of coded problems · Lead manufacturer BECTON DICKINSON MEDICAL SYSTEMS accounts for 58% of manufacturer-tagged reports · Top event location I is 55% of location-tagged rows .

Syringe, Antistick in the event-volume neighbourhood

FDA MAUDE report totals among this device type and nearest nationwide peers

reports

What this shows Syringe, Antistick carries 2,941 MAUDE reports, ranked #414 of 1000.

Source FDA MAUDE via openFDA, aggregated by PlainHospital As of August 2026

Event Types

Malfunction 2,592 (88.1%)
Injury 257 (8.7%)
Other 56 (1.9%)
35 (1.2%)
No answer provided 1 (0.0%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

Other 1,435 (48.6%)
1,336 (45.3%)
Required Intervention 154 (5.2%)
R 10 (0.3%)
O 4 (0.1%)
Death 3 (0.1%)
Hospitalization 3 (0.1%)
Disability 2 (0.1%)
Life Threatening 2 (0.1%)
S 1 (0.0%)
Congenital Anomaly 1 (0.0%)

Top Product Problems

Leak/Splash 520
Break 385
Difficult or Delayed Activation 354
Retraction Problem 316
Fluid/Blood Leak 116
Detachment Of Device Component 101
Use of Device Problem 93
Detachment of Device or Device Component 92
Fail-Safe Problem 92
Device Contamination with Chemical or Other Material 76
Failure to Deliver 69
Defective Device 68
Activation Problem 67
Activation Failure 58
Device Operates Differently Than Expected 54
Defective Component 50
Material Protrusion/Extrusion 49
Device Contaminated During Manufacture or Shipping 47
Device Markings/Labelling Problem 38
Material Separation 38

Yearly Trend

00
2000: 8
01
2001: 17
02
2002: 8
03
2003: 11
04
2004: 13
05
2005: 41
06
2006: 28
07
2007: 21
08
2008: 20
09
2009: 26
10
2010: 34
11
2011: 34
12
2012: 22
13
2013: 27
14
2014: 36
15
2015: 51
16
2016: 94
17
2017: 181
18
2018: 269
19
2019: 497
20
2020: 353
21
2021: 541
22
2022: 170
23
2023: 120
24
2024: 112
25
2025: 148
26
2026: 59

Reports in 2025 (148) held close to the prior two-year average of 116.

Related Entities for Syringe, Antistick

Event Locations

I 1,617 (55.0%)
739 (25.1%)
HOSPITAL 278 (9.5%)
NO INFORMATION 169 (5.7%)
OTHER 54 (1.8%)
NURSING HOME 39 (1.3%)
OUTPATIENT TREATMENT FACILITY 30 (1.0%)
UNKNOWN 6 (0.2%)
HOME 5 (0.2%)
AMBULATORY SURGICAL FACILITY 1 (0.0%)
DIALYSIS CENTER 1 (0.0%)
INVALID DATA 1 (0.0%)
OUTPATIENT DIAGNOSTIC FACILITY 1 (0.0%)

Compare BECTON DICKINSON MEDICAL SYSTEMS vs BD MEDICAL - DIABETES CARE →

Nationwide devices with a comparable report-volume footprint

Syringe, Antistick carries zero death-typed MAUDE reports, so the peer set below compares report volume only; both axes are floored at ≥100 reports so the neighborhood stays in the advertised mass.

Disclaimer: MAUDE figures for Syringe, Antistick are informational only and are not clinical advice. Report codes do not prove device causation. Consult a qualified clinician before acting on this data.

Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. Event-type mix on this page is computed from FDA MAUDE codes for Syringe, Antistick; corpus means use device types with ≥100 reports. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.