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 2017-04-12 for POSEY BED 8060 manufactured by J.t. Posey Company.

Event Text Entries

[72804909] Pt identifier: ni. Evaluation of the return canopy found the slider body is open in a patient access area. The damaged slider was repaired and returned back to the customer for use. Posey beds are multi-use, serviceable items. As such, it is anticipated that the units may occasionally require repair, and as part of standard care the beds should be inspected prior to use. If damage is noted during these routine bed inspections, the unit should not put into use with a patient and should be returned to posey for servicing. If the slider is opened it can potentially leave an unsecured area. Applying pressure directly to the unsecured area would cause the elements to separate, which is why the user manual advises caregivers to apply direct pressure along the entire length of the zipper. If the elements do not have a secure fit when engaged the bed would be render unusable. In order for an open slider to potentially contribute to a patient egress, the following must occur: the open body slider is not noticed, the caregiver does not properly check the elements to ensure there is a secure fit prior to leaving the patient unattended, and 3) the patient identifies the unsecured area, applies pressure against the elements and exits the bed. Following the ifu and standard servicing protocols, the user can identify these issues prior to use and return the bed for repair. In this case, there was no impact or consequence to the patient and the canopy was returned for servicing when the zipper issues were identified. Although it cannot be confirmed, it is possible that routine wear-and-tear from repeated use contributed to the open slider body. Of note, the canopy was 38 months old since its last service. Service issues are trended and reviewed by management on a monthly basis. As part of this monthly review, trends and excursions above control limits will be assessed, documented and acted upon as warranted. No corrective or preventative actions are necessary at this time. Note: the instructions for use warns the user to never use the posey bed if there is damage to the canopy, damage to the accuses panels, or if the entire zipper does not close completely. A failure to follow this warning may lead to serious injury or death from a fall. Always check the canopy and make sure the entire zipper is completely closed before leaving the patient alone to help reduce the risk of a fall or unassisted bed exit. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[72804910] Customer reported the zipper teeth are not aligned on the u side panel. The customer did not specify the date the issue was discovered. No patient or incident reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020362-2017-00011
MDR Report Key6487869
Date Received2017-04-12
Date of Report2017-03-24
Date Mfgr Received2017-03-23
Device Manufacturer Date2013-04-01
Date Added to Maude2017-04-12
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
Manufacturer G1POSEY, S. DE R.L. DE C.V.
Manufacturer StreetAVE FERROCARRILL NO. 16901. BO COLONIAL RIO TIJUANA,3RA. ETAP
Manufacturer CityTIJUANA 22664
Manufacturer CountryMX
Manufacturer Postal Code22664
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 Received2017-04-12
Returned To Mfg2017-03-23
Model Number8060
Catalog Number8060
Lot NumberNA
OperatorOTHER CAREGIVERS
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerJ.T. POSEY COMPANY
Manufacturer Address5635 PECK RD ARCADIA CA 91006 US 91006


Patients

Patient NumberTreatmentOutcomeDate
10 2017-04-12

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.