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PositionPRO 2920 (REF 2920-500-000)Recalls & reported problems

Stryker Corporation · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327277746), received between May 23, 2018 and May 23, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Bent” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Bent1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 23, 2018Bent

    IT WAS REPORTED THE POWER CORD HAD BENT POWER PRONGS. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7537326 ↗

Other MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE devices

All MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.