POWER PRO AMBULANCE COT 6506 6506000000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-01-28 for POWER PRO AMBULANCE COT 6506 6506000000 manufactured by Stryker Medical-kalamazoo.

Event Text Entries

[176869109] This mdr is part of the fda voluntary malfunction summary reporting program. One device was evaluated in the field but the issue was not confirmed; no defect or malfunction was found. 72 devices were evaluated in the field and the issue was confirmed; 49 devices had broken/damaged components, six had bent components, one had a pinched component, two had dirty components, two had loose components, one had an incorrect component, one had a detached component, one was missing a component, and one had an alignment issue, the devices were repaired and returned. One device was not made available for testing by the customer; no cause was established. One device was not evaluated, as the issue was identified and resolved during a troubleshooting call between the customer and stryker technical support. There was no remedial action taken. This device is not labeled for single use.
Patient Sequence No: 1, Text Type: N, H10

[176869110] This report summarizes 50 malfunction events, where it was reported the device was difficult to load/unload. There were 2 events with patient involvement; however, no adverse consequences or clinically significant delay in treatment were reported. There was also 1 instance with caregiver involvement in which the caregiver experienced pain as a result of the event.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: 0001831750-2020-00250
• MDR Report Key: 9637983
• Report Source: COMPANY REPRESENTATIVE
• Date Received: 2020-01-28
• Date of Report: 2020-01-28
• Date of Event: 2020-01-01
• Date Mfgr Received: 2020-01-01
• Date Added to Maude: 2020-01-28
• Event Key: 0
• Report Source Code: Manufacturer report
• Manufacturer Link: Y
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 3
• Reprocessed and Reused Flag: 3
• Health Professional: 3
• Initial Report to FDA: 3
• Report to FDA: 3
• Event Location: 3
• Manufacturer Contact: MR. KRISTEN CANTER
• Manufacturer Street: 3800 EAST CENTRE AVENUE
• Manufacturer City: PORTAGE MI 49002
• Manufacturer Country: US
• Manufacturer Postal: 49002
• Manufacturer Phone: 2693292100
• Manufacturer G1: STRYKER MEDICAL-KALAMAZOO
• Manufacturer Street: 3800 EAST CENTRE AVENUE
• Manufacturer City: PORTAGE MI 49002
• Manufacturer Country: US
• Manufacturer Postal Code: 49002
• Single Use: 3
• Previous Use Code: 3
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: POWER PRO AMBULANCE COT
• Generic Name: STRETCHER, WHEELED
• Product Code: FPO
• Date Received: 2020-01-28
• Model Number: 6506
• Catalog Number: 6506000000
• Device Availability: Y
• Device Eval'ed by Mfgr: Y
• Device Sequence No: 1
• Device Event Key: 0
• Manufacturer: STRYKER MEDICAL-KALAMAZOO
• Manufacturer Address: 3800 EAST CENTRE AVENUE PORTAGE MI 49002 US 49002

Patients

Patient Number	Treatment	Outcome	Date
1	0		2020-01-28