Tool · Post-Market Surveillance

PSUR Report

The vigilance database section of your PSUR, generated in seconds: FDA MAUDE adverse event trends, recalls, and enforcement classifications for your device and similar devices — with the documented, reproducible methodology auditors ask for.

Period
from
to
Leave empty for the last 24 months

Reporting period 2024-072026-06 · FDA data refreshed ~monthly

Product Code: JAK FDA class 2

System, X-Ray, Tomography, Computed

View full classification →
Adverse events in period
410
-22% vs. prior period (523)
Deaths reported
2
Recalls in period
75
Class I enforcement
0

Adverse events per month

2024-07 – 2026-06
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Events by type

Period vs. prior period
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Event type
Period
Prior
Death
2
10
Injury
123
202
Malfunction
270
303
Not specified
15
8

Most reported coded problems

Top 15
Product problems
Count
Device Displays Incorrect Message
109
Application Program Problem
39
Adverse Event Without Identified Device or Use Problem
38
Patient Data Problem
37
Use of Device Problem
24
No Apparent Adverse Event
23
Improper or Incorrect Procedure or Method
18
Computer Software Problem
17
Appropriate Device Problem Term/Code Not Available
17
Device Operational Issue
15
Connection Problem
15
Failure to Advance
14
Material Fragmentation
12
Insufficient Device Problem Information
12
Application Network Problem
12
Patient problems
Count
No Clinical Signs, Symptoms or Conditions
267
Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
38
Pneumothorax
26
Insufficient Information
26
Laceration(s)
12
Limb Fracture
10
Abrasion
9
Hemorrhage/Blood Loss/Bleeding
8
Unintended Radiation Exposure
5
Respiratory Failure
3
Pain
3
Limb Pain
3
Fistula
3
Fever
3
Crushing Injury
3

Recalls in period

75 total
FDA enforcement classification: Class II: 81
Date
Recalling firm
Status
2026-03-26
Open, Classified
2026-03-26
Open, Classified
2026-03-26
Open, Classified
2026-03-26
Open, Classified
2026-03-26
Open, Classified
2026-03-26
Open, Classified
2026-03-26
Open, Classified
2026-03-07
Open, Classified
2026-02-03
Open, Classified
2026-01-07
Open, Classified
2026-01-07
Open, Classified
2026-01-07
Open, Classified
2026-01-07
Open, Classified
2025-12-19
Open, Classified
2025-12-19
Open, Classified
2025-12-19
Open, Classified
2025-12-19
Open, Classified
2025-12-04
Open, Classified
2025-12-04
Open, Classified
2025-12-03
Open, Classified
2025-10-29
Open, Classified
2025-10-29
Open, Classified
2025-09-25
Open, Classified
2025-09-25
Open, Classified
2025-09-25
Open, Classified
2025-09-12
Open, Classified
2025-09-12
Open, Classified
2025-09-12
Open, Classified
2025-09-12
Open, Classified
2025-09-12
Open, Classified
2025-09-12
Open, Classified
2025-09-12
Open, Classified
2025-09-12
Open, Classified
2025-09-12
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-08-13
Open, Classified
2025-05-29
Open, Classified
2025-05-23
Open, Classified
2025-04-01
Open, Classified
2025-02-28
Open, Classified
2025-02-18
Open, Classified
2025-02-18
Open, Classified
2025-02-18
Open, Classified
2025-02-18
Open, Classified
2025-02-18
Open, Classified
2025-02-18
Open, Classified
2025-02-18
Open, Classified
2024-11-16
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-11-05
Open, Classified
2024-08-08
Open, Classified
2024-08-05
Completed

Adverse events by year

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Methodology & data provenance

For your PSUR appendix

Search protocol: FDA MAUDE adverse event reports, FDA device recalls, and FDA enforcement reports (openFDA datasets) were queried for product code JAK, reporting period 2024-07 to 2026-06 (prior comparison period 2022-07 to 2024-06).

Data coverage: adverse event data for these product codes extends through 2026-05. Source openFDA export dated 2026-06-30. Recall records with missing or implausible initiation dates (0 for these codes) are excluded from period counts.

Generated: 2026-07-05 22:07 UTC by BEUDAMED (beudamed.com/fda/psur-report). Dataset sizes: 25,039,198 adverse events, 58,607 recalls, 39,365 enforcement reports.

PSUR database searches, explained

Under the EU MDR, manufacturers must produce a Periodic Safety Update Report (PSUR) (Class IIa and above; a PMS report for Class I) on a defined schedule. A required part of that report is a survey of publicly available vigilance data — most importantly the FDA's MAUDE adverse event database and FDA recall records — covering both your own device and similar devices on the market (the "state of the art").

Doing this by hand means repeated MAUDE queries, manual export, deduplication, and trending — hours of work per report, repeated every reporting period. This tool runs the same search protocol in seconds and documents it: which datasets were queried, with which filters, when, and with what coverage — so the search is reproducible, which is exactly what a Notified Body auditor wants to see.

Event counts are grouped by the FDA's reported event type (death, injury, malfunction). Name-based device matching is clearly labeled as indicative: only you can confirm whether a specific MAUDE report concerns your device. Recall records with implausible dates are excluded and the exclusion is disclosed. All data is from the official openFDA datasets and refreshed approximately monthly.