Air+ 2863-000-000Recalls & reported problems
Stryker Corporation · Class 2
All models of AIR+ (4)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613327499735), received between Feb 12, 2021 and Apr 23, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (5 reports).
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
- Electrical /Electronic Property Problem5
- Sharp Edges1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2026Electrical /Electronic Property Problem
THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. EVENTS OCCURRED BETWEEN JANUARY 1- MARCH 31, 2026. THIS REPORT SUMMARIZES 1 MALFUNCTION EVENTS(S), WHERE IT WAS REPORTED THE DEVICES EXPERIENCED ACCESSIBLE AC CURRENT. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24966488 ↗MalfunctionApr 28, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED ACCESSIBLE AC CURRENT. NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21919250 ↗MalfunctionOct 28, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED ACCESSIBLE AC CURRENT. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20544807 ↗MalfunctionJul 19, 2023Sharp Edges; Sharp Edges
THIS REPORT SUMMARIZES 0 MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE EXPERIENCED SHARP METAL EDGES. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17350416 ↗MalfunctionFeb 12, 2021Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
IT WAS REPORTED THE DEVICE HAD ACCESSIBLE AC CURRENT. NO ADVERSE CONSEQUENCES RELATED TO THE EVENT WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11322352 ↗MalfunctionFeb 12, 2021Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
IT WAS REPORTED THE DEVICE HAD ACCESSIBLE AC CURRENT. NO ADVERSE CONSEQUENCES RELATED TO THE EVENT WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11322341 ↗
Other BED, FLOTATION THERAPY, POWERED devices
- Compella™Bariatric Bed P7800AHill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED1 recall1 death362 reports
- pro+ P7924A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED4 recalls3 reports
- pro+ P7924ARENT01Hill-Rom, Inc. · Bed, Flotation Therapy, Powered3 recalls1 death15 reports
- pro+ P3255A02Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls8 reports
- pro+ P7924A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls4 reports
- pro+ P3255A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls3 reports
- pro+ P7923A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls2 reports
- pro+ P7923A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls0 reports
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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