MalfunctionNZD
MEDLINE STRETCHER
Received Nov 21, 2023
Report MW5148409 · MDR key 18194232
Device
Generic name
Stretcher, Patient Restraint
Manufacturer
Medline Industries, Lp - NorthfieldPatient
Unknown
- Insufficient Information
- Insufficient Information
Narrative
Description of Event or Problem
(B)(6) WAS NOTIFIED OF A POTENTIALLY REPORTABLE COMPLAINT INVOLVING A PRODUCT FOR WHICH (B)(6) IS NOT THE ORIGINAL EQUIPMENT MANUFACTURER OF THE REPORTED DEVICE. THE CUSTOMER ALLEGED A MANUFACTURER MEDLINE STRETCHER, SERIAL NUMBER (B)(6) THAT HAD A FOOTREST THAT WOULD NOT SUPPORT WEIGHT AND A COSMETICALLY DAMAGED CALF SUPPORT. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).