FLEXITIME LIGHT FLOW 1 X (2 X 50 ML) 40005040Recalls & reported problems
Kulzer GmbH · Material, Impression · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI J014400050400), received between Oct 19, 2023 and Oct 19, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method1
Patient problems
- Dyspnea1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 19, 2023Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
PATIENT WAS REPORTED TO HAVE AN ALLERGIC TYPE REACTION OF MILD RESPIRATORY DIFFICULTY APPROXIMATELY 1 HOUR AFTER EXPOSURE TO 2 PRODUCTS.
Patient problems: Dyspnea
MAUDE report 17963202 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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