POSEY 8282WLRecalls & reported problems
Posey Products, LLC · Wireless Nurse Call Adapter · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00190676007646), received between Dec 13, 2023 and Jan 31, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “No Audible Alarm” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- No Audible Alarm2
- Loss of Power1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 31, 2025No Audible Alarm; No Audible Alarm
CUSTOMER REPORTING A COMPLAINT ON PRODUCT 8645WL QTY 3, 8282WL WE DO NOT HAVE LOT #'S. ALARM #1 DID NOT ALARM WHEN PATIENT GOT UP. UNKNOWN IF SENSOR WAS PAIRED CORRECTLY. PATIENT FALL. NEW ALARM SWAPPED AND 2ND ALARM FAILED TO SOUND TOO WHICH IS ALARM #2. THESE WERE BOTH IN RM 478. NO INJURY FROM 2ND OR 1ST FALL. PRODUCT 8282WL KEPT TRIGGERING THE NURSE CALL SYSTEM FALSELY. COULD NOT BE CORRECTED UNTIL A DIFFERENT 8282WL WAS TESTED. 3RD ALARM GAVE AUDIBLE WARNING THAT MAINT WAS REQ'D. IT WOULD NOT ALARM WHEN PATIENT GOT OUT OF CHAIR. NO FALLS. TRIGGERED CHAIR EXIT ALARM WHILE PATIENT WAS LYING IN BED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21288905 ↗MalfunctionMay 22, 2024No Audible Alarm; No Audible Alarm
CUSTOMER REPORTING A COMPLAINT ON PRODUCT #'S 8645WL, 8282WL, & 8309WL. CUSTOMER STATES THAT A FALL OCCURRED WITH NO ALARM SOUNDING. WHEN THE STAFF TESTED THE ALARM THEY NOTICED THAT IT WOULD PAIR AND THEN DETACH WITHOUT SOUNDING AN ALARM OR VOICE/NOISE SOUNDING. THE PAD WAS NOT KEPT & WAS DISCARDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19370586 ↗MalfunctionDec 13, 2023Loss of Power; Loss of Power
A CUSTOMER REPORTED THAT THEY HAVE EXPERIENCED AN INCREASE IN FALL RATES OVER THE LAST THREE MONTHS DUE TO BATTERIES IN THE ALARM BECOMING DEPLETED. STAFF STATED THEY COULD NOT CHANGE THE BATTERIES DUE TO THE BATTERY DOORS BEING TOO DIFFICULT TO OPEN. THE CUSTOMER ALSO STATED THAT FAIL RATES HAVE INCREASED TOO DUE TO THE NURSE CALL ADAPTER NOT ALERTING THE NURSE CALL SYSTEM. ALSO, THEY STATED THAT THEY WERE NOT GETTING LOW BATTERY NOTIFICATION DUE TO NOT BEING ABLE TO REPLACE THE BATTERIES. THE CUSTOMER STATED THAT THERE HAVE BEEN MULTIPLE PATIENT INCIDENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18320016 ↗
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- POSEY 8399Posey Products, LLC · Monitor, Bed Patient19 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.