PENDING MMPF1110TRecalls & reported problems
Medline Industries, Inc. · PIN, TEMP FIX, THREADED MINI, 1.1 X 10MM · Class 2
All models of PENDING (5)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196690886), received between Apr 20, 2022 and May 26, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (2 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 16, 2026.
Most reported problems
Device problems
- Break2
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 26, 2022Break
ACCORDING TO THE FACILITY DURING A PROCEDURE THE 'BB TAKS BROKE INSIDE THE PATIENT AND HAD TO REMOVED'.
Patient problems: Foreign Body In Patient
MAUDE report 14516214 ↗InjuryApr 20, 2022Break
ACCORDING TO THE FACILITY DURING A PROCEDURE THE 'BB TAKS BROKE INSIDE THE PATIENT AND THE DOCTOR HAD TO REMOVE THEM'.
Patient problems: Foreign Body In Patient
MAUDE report 14160651 ↗
Other Trousers, anti-shock devices
- Harmony 74016261Smith & Nephew, Inc. · Trousers, anti-shock2 reports
- PROPHECY INBONE PTA00050Wright Medical Technology, Inc. · Trousers, anti-shock1 report
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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