2026 data FDA MAUDE openFDA

Colorimeter, Photometer, Spectrophotometer For Clinical Use

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 MAUDE casebook

openFDA event book Colorimeter LIGHT-BOOK · MAUDE

#995 of 1000 · 348 reports · 1999–2026

  • BOOK 348 reports
  • RANK #995 of 1000
  • DEATH 1 death-typed
  • INJ 8 injury-typed
  • MALF 294 malfunction
  • SPAN 1999–2026
  • PEAK 2014: 69
  • PHOTO Light

Nearest event-volume peer: Light, Surgical, Accessories (1 report gap)

Colorimeter, Photometer, Spectrophotometer For Clinical Use sits #995 of 1000 among tracked device types with 348 MAUDE reports spanning 1999–2026. 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 →

Event-type mix vs corpus

Shares of FDA event_type codes on this device type, compared with the mean across 1,000 device types that have ≥100 MAUDE reports. Codes are report labels, not adjudicated causation.

  • DEATH 0.3% corpus 1.5% · below corpus mean (-1.2 pp)
  • INJ 2.3% corpus 30.4% · below corpus mean (-28.1 pp)
  • MALF 84.5% corpus 64.5% · above corpus mean (+20.0 pp)

Lead product-problem code Incorrect, Inadequate or Imprecise Result or Readings is 27% of coded problems · Lead manufacturer SIEMENS HEALTHCARE DIAGNOSTICS INC. accounts for 46% of manufacturer-tagged reports · Top event location is 89% of location-tagged rows .

Colorimeter in the event-volume neighbourhood

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

reports

What this shows Colorimeter, Photometer, Spectrophotometer For Clinical Use carries 348 MAUDE reports, ranked #995 of 1000.

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

Event Types

Malfunction 294 (84.5%)
Other 39 (11.2%)
Injury 8 (2.3%)
6 (1.7%)
Death 1 (0.3%)

Patient Outcomes

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

328 (94.0%)
Other 12 (3.4%)
Required Intervention 6 (1.7%)
Death 2 (0.6%)
O 1 (0.3%)

Top Product Problems

Incorrect, Inadequate or Imprecise Result or Readings 28
False Positive Result 18
False Negative Result 11
Fire 6
Smoking 6
Adverse Event Without Identified Device or Use Problem 4
Calibration Problem 4
Low Readings 4
Mechanical Problem 3
Use of Device Problem 3
Device Operates Differently Than Expected 2
Electrical /Electronic Property Problem 2
Electrical Shorting 2
Excessive Heating 2
Insufficient Information 2
Low Test Results 2
Noise, Audible 2
High Readings 1
Material Integrity Problem 1
Melted 1

Yearly Trend

99
1999: 3
00
2000: 2
01
2001: 7
02
2002: 6
03
2003: 7
04
2004: 7
05
2005: 6
06
2006: 2
07
2007: 1
08
2008: 4
09
2009: 10
10
2010: 46
11
2011: 6
12
2012: 3
13
2013: 63
14
2014: 69
15
2015: 13
16
2016: 9
17
2017: 10
18
2018: 2
19
2019: 1
21
2021: 3
22
2022: 22
23
2023: 14
24
2024: 7
25
2025: 21
26
2026: 4

Related Entities for Colorimeter, Photometer, Spectrophotometer For Clinical Use

Event Locations

311 (89.4%)
I 27 (7.8%)
NOT APPLICABLE 5 (1.4%)
OTHER 2 (0.6%)
INVALID DATA 1 (0.3%)
OUTPATIENT TREATMENT FACILITY 1 (0.3%)
UNKNOWN 1 (0.3%)

Compare SIEMENS HEALTHCARE DIAGNOSTICS INC. vs BECTON, DICKINSON & CO. (SPARKS) →

Nationwide devices with similar MAUDE profiles

Two openFDA-derived peer sets for Colorimeter, both floored at ≥100 reports so the neighborhoods stay in the advertised mass.

Similar report volume

Nearest other device types by FDA MAUDE report count (348 here).

Similar death-typed counts

Nearest other device types by death-typed report count (1 here), distinct from the volume row.

Disclaimer: MAUDE figures for Colorimeter 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 Colorimeter; 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.