POSEY BED 8070

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-10-26 for POSEY BED 8070 manufactured by Jt Posey Company.

Event Text Entries

[29872279] Inspection of the unit found an open zipper slider on the patient access window. 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 zipper slider body is bent open (i. E. , the mouth is wider than manufacturing specifications) it can prevent the slider from properly engaging the zipper teeth. In areas where the slider engages the teeth, the zipper is secure and cannot be opened. However, if the teeth do not engage it can potentially leave an unsecured area. Applying pressure directly to the unsecured area will reveal the breach, which is why the user manual advises caregivers to apply direct pressure along the entire length of the zipper. In order for an open slider to potentially contribute to patient egress, the following must occur: the slider does not engage the teeth, the caregiver does not properly check the zipper prior to leaving the patient unattended, and the patient identifies the unsecured area and exits the bed. Following the ifu and standard servicing protocols, the user can identify any open sliders 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 the cause of the open slider cannot be confirmed, it is possible that an excessive amount of force was applied to the pull tab, which could have bent the slider body open. Of note, the canopy was 30 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. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[29872280] Customer reported the teeth will not stay aligned when the zipper is closed. Customer reported damage to the teeth and slider. No patient incident or injury was reported and the date of the discovery is unknown.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020362-2015-00071
MDR Report Key5179065
Date Received2015-10-26
Date of Report2015-10-23
Date Mfgr Received2015-10-23
Device Manufacturer Date2010-10-04
Date Added to Maude2015-10-26
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. FERROCARRIL NO. 16901. BO COLONIA RIO TIJUANA, 3RA. ETAP
Manufacturer CityTIJUANA, MEXICO 22664
Manufacturer CountryMX
Manufacturer Postal Code22664
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePOSEY BED 8070
Generic NamePATIENT BED WITH CANOPY/RESTRAINTS
Product CodeOYS
Date Received2015-10-26
Returned To Mfg2015-10-15
Model Number8070
Catalog Number8070
Lot Number2010100401
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerJT POSEY COMPANY
Manufacturer Address5635 PECK ROAD ARCADIA CA 910060020 US 910060020


Patients

Patient NumberTreatmentOutcomeDate
10 2015-10-26

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