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..
[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
Report Number | 0001526350-2020-00115 |
MDR Report Key | 9644753 |
Report Source | USER FACILITY |
Date Received | 2020-01-29 |
Date of Report | 2020-01-29 |
Date of Event | 2019-12-28 |
Date Mfgr Received | 2020-01-03 |
Date Added to Maude | 2020-01-29 |
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 |
Reporter Occupation | RISK MANAGER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. CHRISTINA ARNT |
Manufacturer Street | 56 E. BELL DRIVE |
Manufacturer City | WARSAW IN 46582 |
Manufacturer Country | US |
Manufacturer Postal | 46582 |
Manufacturer Phone | 5745273773 |
Manufacturer G1 | ZIMMER SURGICAL, INC. |
Manufacturer Street | 200 WEST OHIO AVENUE |
Manufacturer City | DOVER OH 44622 |
Manufacturer Country | US |
Manufacturer Postal Code | 44622 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ATS4000TS WITH HOSES |
Generic Name | TOURNIQUET, PNEUMATIC |
Product Code | KCY |
Date Received | 2020-01-29 |
Model Number | N/A |
Catalog Number | 60-4000-101-00 |
Lot Number | N/A |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ZIMMER SURGICAL, INC. |
Manufacturer Address | 200 WEST OHIO AVENUE DOVER OH 44622 US 44622 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-01-29 |