FDA Adverse Event Malfunction Summary report: N

PRIME CARE (R) TRANSCEND MATTRESS

MDR report key: 4190178 · Received September 18, 2014

Report

Report Number
3007538326-2014-00085
Event Type
Malfunction
Date Received
September 18, 2014
Date of Event
August 22, 2014
Report Date
September 16, 2014
Manufacturer
PRIMUS MEDICAL LLC
Product Code
IKY
Removal / Correction Number
Z-2596-2014
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

UPON INSPECTION OF THIS MATTRESS, THE URETHANE COVER BUBBLED THROUGHOUT THE ENTIRE MATTRESS COVER EXPOSING THE INSIDE OF THE TOP COVER OF THE MATTRESS. THE FIRM IS IN THE PROCESS OF DELIVERING NEW MATTRESSES TO THE FACILITY. THIS PROBLEM HAS BEEN ASSIGNED TO CAPA #(B)(4), AND A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE CORRECTIVE ACTION.

Description of Event or Problem · 1

UPON RECEIPT OF THE RECALL PACKET, THE CUSTOMER NOTIFIED THE FIRM THEY HAD A DELAMINATED MATTRESS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
578151 PRIME CARE (R) TRANSCEND MATTRESS IKY PRIMUS MEDICAL LLC TCM4280 053013

Patients

Seq Age Sex Outcome Treatment
1