inforMED
MalfunctionFMP

WEDGIE - 3"X4"X5"

Received Sep 24, 2014

Report 1218950-2014-07330 · MDR key 4309731

Device

Model number

91014

Lot number

LOT CODE NOT PROVIDED - NO

Product problems

  • Device Contamination with Chemical or Other Material

Patient

Not reported

  • No Known Impact Or Consequence To Patient

Narrative

Description of Event or Problem

THE CUSTOMER REPORTED MOLD ON THE WEDGIE PRODUCT. NO PT INCIDENT/INJURY WAS REPORTED.

Additional Manufacturer Narrative

(B)(4). THE CUSTOMER REPORTED MOLD ON THE WEDGIE PRODUCT. NO PT INCIDENT/INJURY WAS REPORTED. THIS COMPLAINT IS BEING REPORTED, AS NO MATERIAL IS AVAILABLE FOR EVAL TO CONFIRM THAT THERE IS NO MOLD IN/ON THE PRODUCT. THERE IS NO CURRENT EVIDENCE THAT MOLD WILL GROW INSIDE THE WEDGIE PRODUCT (GEL MATRIX). THERE IS NO EVIDENCE OF GEL "SWEATING" THROUGH THE BLADDER FOR MOLD TO GROW ON THE OUTSIDE OF THE BLADDER. THE BLADDER IS MADE OF VINYL, WHICH IS A DIFFERENT MATERIAL FROM THAT USED FOR THE GEL-E DONUT PRODUCT. NO PRODUCT MALFUNCTION CAN BE CONFIRMED/DETERMINED, AS NO MATERIAL IS AVAILABLE FOR EVAL/TESTING.