ASSISTARM AA-PSN100Recalls & reported problems
Conmed Corporation · AssistArm Surgical Positioner · Class 1
- 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 10845854043578), received between Nov 30, 2023 and Nov 30, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Mechanical Jam” (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.
Reports received per month
Most reported problems
Device problems
- Mechanical Jam1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 30, 2023Mechanical Jam; Mechanical Jam
THE CUSTOMER REPORTED THAT THE DEVICE, AA-PSN100, ASSISTARM SURGICAL POSITIONER, WAS BEING PRE-OP TESTED FOR A SHOULDER ORIF PROCEDURE ON 1NOV23 WHEN IT WAS REPORTED, ¿POSITIONER WAS STUCK WHEN TRYING TO USE PEDAL TO ADJUST. USER ADJUSTED MANUALLY AND POSITIONER MOVED AND CAUGHT USERS FINGER. TUFTS FRACTURE ON LEFT HAND RING FINGER OF USER.¿. THERE WAS NO REPORT OF MEDICAL INTERVENTION OR HOSPITALIZATION FOR THE USER. FURTHER ASSESSMENT QUESTIONS HAVE NOT BEEN ANSWERED TO DATE. THE PROCEDURE WAS COMPLETED AS PLANNED WITH NO DELAY BEING REPORTED. THIS REPORT IS BEING RAISED DUE TO THE REPORTED INJURY OF USER LEFT HAND RING FINGER BEING FRACTURED.
Patient problems: Bone Fracture(s)
MAUDE report 18236051 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.