POSEY 8282Recalls & reported problems
Posey Products, LLC · NURSE CALL CABLE · Class 1
- Adverse event reports
- 3
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10190676002044), received between Apr 10, 2024 and Jun 9, 2026 — classified as 1 death, 2 malfunctions.
The most frequently reported specific device problem is “No Audible Alarm” (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
Most reported problems
Device problems
- No Audible Alarm3
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
DeathJun 9, 2026No Audible Alarm
ON 5/13/2026, A COMPLAINT WAS REPORTED THAT A PATIENT WAS FOUND OUT OF A CHAIR AFTER AMBULATING TO THE BATHROOM AND HAD REMOVED A PICC LINE, RESULTING IN FLUID EXPOSURE. THE PATIENT WAS ALSO ATTEMPTING TO INSERT DENTURES. THE POSEY ALARM WAS ACTIVE (GREEN LIGHT ON) BUT DID NOT ALERT WHEN THE PATIENT EXITED THE CHAIR. STAFF CONFIRMED THE ALARM REMAINED ACTIVE DESPITE THE EVENT. THE PATIENT WAS LATER TRANSFERRED TO HOSPICE AND SUBSEQUENTLY PASSED AWAY.
Patient problems: Insufficient Information
MAUDE report 25443138 ↗MalfunctionAug 15, 2024No Audible Alarm; No Audible Alarm
CUSTOMER REPORTED ISSUE WITH NURSE CALL CORD NOT WORKING TO RING OUT TO NURSE CALL SYSTEM. THE ISSUE IS ISOLATED TO ONE UNIT REPORTING RANDOM OCCURRENCES. THE CUSTOMER AND FACILITY ENGINEER CONDUCTED INITIAL TESTING TO DETERMINE THAT THE NURSE CALL CORD WAS NOT WORKING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19997648 ↗MalfunctionApr 10, 2024No Audible Alarm; No Audible Alarm
CUSTOMER REPORTING A COMPLAINT ON PRODUCT # 8645 & 8282. CUSTOMER STATES THE PRODUCTS WERE IN USE AND DID NOT TRIGGER THE NURSE CALL SYSTEM WHEN A PATIENT GOT UP FROM THEIR CHAIR. THIS RESULTED IN A FALL. NO INJURIES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19083185 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.