CUB PEDIATRIC CRIB- HYD BASE FL19H

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-12 for CUB PEDIATRIC CRIB- HYD BASE FL19H manufactured by Stryker Medical-kalamazoo.

Event Text Entries

[123806360] It was reported that the siderail assist cable was broken. No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: 0001831750-2018-01096
• MDR Report Key: 7962626
• Date Received: 2018-10-12
• Date of Report: 2018-10-12
• Date of Event: 2018-09-18
• Date Mfgr Received: 2018-09-18
• Device Manufacturer Date: 2009-04-02
• Date Added to Maude: 2018-10-12
• 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. BRIAN THOMPSON
• 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: 0

Device Details

• Brand Name: CUB PEDIATRIC CRIB- HYD BASE
• Generic Name: BED, PEDIATRIC OPEN HOSPITAL
• Product Code: FMS
• Date Received: 2018-10-12
• Catalog Number: FL19H
• 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		2018-10-12