ATS4000TS WITH HOSES N/A 60-4000-101-00

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-29 for ATS4000TS WITH HOSES N/A 60-4000-101-00 manufactured by Zimmer Surgical, Inc..

Event Text Entries

[177147866] This event has been recorded by zimmer biomet under (b)(4). The investigation is still in progress. Once the investigation is complete a follow up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[177147867] It was reported that the right arm tourniquet was inflated at 1240 and deflated at 1305. At 1416, the tourniquet was noted to be inflated to 250 mm/hg. The tourniquet was not inflated by any team member, but had been inflated for 17 minutes. The tourniquet was removed and taken out of service.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001526350-2020-00115
MDR Report Key9644753
Report SourceUSER FACILITY
Date Received2020-01-29
Date of Report2020-01-29
Date of Event2019-12-28
Date Mfgr Received2020-01-03
Date Added to Maude2020-01-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. CHRISTINA ARNT
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745273773
Manufacturer G1ZIMMER SURGICAL, INC.
Manufacturer Street200 WEST OHIO AVENUE
Manufacturer CityDOVER OH 44622
Manufacturer CountryUS
Manufacturer Postal Code44622
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameATS4000TS WITH HOSES
Generic NameTOURNIQUET, PNEUMATIC
Product CodeKCY
Date Received2020-01-29
Model NumberN/A
Catalog Number60-4000-101-00
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerZIMMER SURGICAL, INC.
Manufacturer Address200 WEST OHIO AVENUE DOVER OH 44622 US 44622


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-29

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