MAUDE Adverse Event Report: STRYKER MEDICAL-KALAMAZOO ULTRA COMFORT, SE 3 X 30; MATTRESS, FLOTATION THERAPY, NON-POWERED

Catalog Number 1703034300

Device Problem Device Slipped (1584)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Date 11/09/2017

Event Type  malfunction  

Event Description

It was reported that the mattress was sliding off from the stretcher surface during patient transfers.The patient was not affected and no adverse consequence or clinically relevant delay in treatment was reported.

Manufacturer Narrative

Information provide by the user facility identified that the user facility was using a one person transfer method.This may be attributed to customer preference as the customer was dissatisfied with the movement of the mattress during patient transfers during this transfer method.The user facility was provided instructions on properly securing the mattresses.

Event Description

It was reported that the mattress was sliding off from the stretcher surface during patient transfers.The patient was not affected and no adverse consequence or clinically relevant delay in treatment was reported.

Manufacturer Narrative

Supplemental submitted to include udi.

Event Description

It was reported that the mattress was sliding off from the stretcher surface during patient transfers.The patient was not affected and no adverse consequence or clinically relevant delay in treatment was reported.

• Brand Name: ULTRA COMFORT, SE 3 X 30
• Type of Device: MATTRESS, FLOTATION THERAPY, NON-POWERED
• Manufacturer (Section D): STRYKER MEDICAL-KALAMAZOO; 3800 east centre avenue; portage MI 49002
• Manufacturer (Section G): STRYKER MEDICAL-KALAMAZOO; 3800 east centre avenue; portage MI 49002
• Manufacturer Contact: kristen canter ; 3800 east centre avenue; portage, MI 49002 ; 2693292100
• MDR Report Key: 7114648
• MDR Text Key: 95074522
• Report Number: 0001831750-2017-00563
• Device Sequence Number: 1
• Product Code: IKY
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: user facility
• Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date: 03/23/2018

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
• Device Operator: No Information
• Device Catalogue Number: 1703034300
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 12/13/2017
• Initial Date FDA Received: 12/13/2017
• Supplement Dates Manufacturer Received: 12/13/2017; 12/13/2017
• Supplement Dates FDA Received: 02/01/2018; 03/23/2018
• Was Device Evaluated by Manufacturer?: No
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1