MAUDE Adverse Event Report: STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP COLOR CUFF NON-STERILE DISPOSABLE TOURNIQUET CUFF 30.0 INCH X 4.0 INCH; TOURNIQUET, PNEUMATIC

Catalog Number	5921-030-235NS
Medical Device Problem Code	Decrease in Pressure (1490)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/22/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Reported events: 8 events were reported for this quarter.Product return status: 3 devices were not available for evaluation.5 device investigation types have not yet been determined.Additional information: 8 devices were labeled for single-use.8 devices were not reprocessed or reused.
Event or Problem Description
This report summarizes 8 malfunction events in which the device reportedly had a decrease in pressure.1 event had no patient involvement; no patient impact.7 events had patient involvement; no patient impact.
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Supplemental rationale: 8 previously reported events are included in this follow-up record.Product return status: 1 device was received.3 devices were not available for evaluation.4 device investigation types have not yet been determined.
Event or Problem Description
This report summarizes 8 malfunction events in which the device reportedly had a decrease in pressure.1 event had no patient involvement; no patient impact.7 events had patient involvement; no patient impact.
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Supplemental rationale: 8 previously reported events are included in this follow-up record.Product return status 1 device was received.4 devices were not available for evaluation.3 devices were evaluated based on historical data analysis.
Event or Problem Description
This report summarizes 8 malfunction events in which the device reportedly had a decrease in pressure.1 event had no patient involvement; no patient impact.7 events had patient involvement; no patient impact.

• Brand Name: COLOR CUFF NON-STERILE DISPOSABLE TOURNIQUET CUFF 30.0 INCH X 4.0 INCH
• Common Device Name: TOURNIQUET, PNEUMATIC
• Manufacturer (Section D): STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP; 1941 stryker way; portage MI 49002
• Manufacturer (Section G): STRYKER INSTRUMENTS-PUERTO RICO; las palmas industrial park; highway #3, km 130.2; arroyo 00615 ; * 00615
• Manufacturer Contact: colette chung ; 1941 stryker way; portage, MI 49002 ; 2693237700
• MDR Report Key: 16500403
• Report Number: 3015967359-2023-00519
• Device Sequence Number: 3301743
• Product Code: KCY
• UDI-Device Identifier: 37613327606196
• UDI-Public: 37613327606196
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• Number of Events Summarized: 8
• Summary Report (Y/N): Y
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Remedial Action: Recall
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 07/27/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Catalogue Number: 5921-030-235NS
• Device Lot Number: VMSR
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/22/2023
• Supplement Date Received by Manufacturer: 02/22/2023; 02/22/2023
• Initial Report FDA Received Date: 03/07/2023
• Supplement Report FDA Received Date: 04/10/2023; 07/27/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: 3228500
• Patient Sequence Number: 1
• Patient Sex: Unknown