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Posey 8060Recalls & reported problems

Tidi Products, LLC · BCS W/ SUPPORT SURFACE · Class 1

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00618125192250), received between Mar 6, 2025 and Apr 2, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (3 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 3 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Mechanical Problem3
  • Material Puncture/Hole1

Patient problems

  • No Clinical Signs, Symptoms or Conditions4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 2, 2026Material Puncture/Hole

    A PATIENT WAS ABLE TO EXIT THE ENCLOSURE BED BY MANIPULATING THE ZIPPERS FROM THE INSIDE OF THE CANOPY. NO INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24768997 ↗
  • MalfunctionMar 6, 2025Mechanical Problem; Mechanical Problem

    S/N (B)(6) HAS ZIPPER DAMAGE, ZIPPER SPLITTING RIGHT SIDE PANEL.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21536637 ↗
  • MalfunctionMar 6, 2025Mechanical Problem; Mechanical Problem

    S/N (B)(6) HAS ZIPPER DAMAGE, ZIPPER SPLIT ON THE LEFT SIDE PANEL.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21536609 ↗
  • MalfunctionMar 6, 2025Mechanical Problem; Mechanical Problem

    S/N (B)(6) HAS ZIPPER DAMAGE, ZIPPER SPLIT ON LEFT SIDE PANEL.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21536601 ↗

Other Patient Bed With Canopy/Restraints devices

All Patient Bed With Canopy/Restraints devices →

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