POSEY BED 8060

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-01-25 for POSEY BED 8060 manufactured by Posey Products Llc.

Event Text Entries

[98436701] Product is scheduled to be returned but has not been received in for evaluation at the time of this report. Therefore, this report is based solely on the information provided by the customer. At this time there is not evidence that a manufacturing non-conformity contributed to the reported complaint and the instructions for use were reviewed and determined to provide adequate instructions and warning for the safe and effective use of the device. Therefore, no corrective or preventative actions are necessary. All complaints are trended and reviewed by management on a monthly basis. As part of this monthly review, any excursion above the control limits for this failure mode will be assessed, documented and acted upon as warranted. (b)(4). No product returned at this time.
Patient Sequence No: 1, Text Type: N, H10


[98436702] Customer reported the patient was found on the floor and the zipper was found open. The nurse believes the patient fell due to the equipment not being zipped up. No patient injuries and no medical attention required.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020362-2018-00005
MDR Report Key7220111
Date Received2018-01-25
Date of Report2018-03-08
Date of Event2018-01-14
Date Mfgr Received2018-03-08
Device Manufacturer Date2014-08-14
Date Added to Maude2018-01-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactWILLIAM HINCY
Manufacturer StreetPOSEY COMPANY 5635 PECK ROAD
Manufacturer CityARCADIA CA 91006
Manufacturer CountryUS
Manufacturer Postal91006
Manufacturer Phone6264433143
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report0

Device Details

Brand NamePOSEY BED 8060
Generic NamePATIENT BED WITH CANOPY/RESTRAINTS
Product CodeOYS
Date Received2018-01-25
Model Number8060
Catalog Number8060
Lot NumberNA
OperatorNURSE
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerPOSEY PRODUCTS LLC
Manufacturer Address5635 PECK RD ARCADIA CA 91006 US 91006


Patients

Patient NumberTreatmentOutcomeDate
10 2018-01-25

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