MAUDE Adverse Event Report: STRYKER MEDICAL-KALAMAZOO M-1 COT KNEE GATCH LITTER; STRETCHER, WHEELED

Model Number	6100
Medical Device Problem Code	Device Fell (4014)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/01/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This record is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program.1 device is pending evaluation.There was no remedial action taken.  this device is not labeled for single use.
Event or Problem Description
This report summarizes 1 malfunction event, where it was reported there was a fowler collapse.There was no patient involvement.
Event or Problem Description
It was originally reported that 1 event occurred where there was a fowler collapse; however, upon completion of the final investigation, the device was experiencing a gatch collapse, which is not reportable.There was no patient involvement.
Additional Manufacturer Narrative
Upon evaluation, it was determined the device experienced a gatch collapse, which is not reportable.

• Brand Name: M-1 COT KNEE GATCH LITTER
• Common Device Name: STRETCHER, WHEELED
• Manufacturer (Section D): STRYKER MEDICAL-KALAMAZOO; 3800 east centre avenue; portage MI 49002
• MDR Report Key: 11710779
• Report Number: 0001831750-2021-00706
• Device Sequence Number: 17117269
• Product Code: FPO
• UDI-Device Identifier: 07613327261561
• UDI-Public: 07613327261561
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): Y
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 05/26/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: No Information
• Device Model Number: 6100
• Device Catalogue Number: 6100031000
• Was Device Available for Evaluation?: Yes
• Initial Date Received by Manufacturer: 04/01/2021
• Supplement Date Received by Manufacturer: 04/01/2021
• Initial Report FDA Received Date: 04/22/2021
• Supplement Report FDA Received Date: 05/26/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1