Stryker Corporation Recall 91849
Description: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4,1BLA,2PRT QUICK Catalog number: 5921-030-235NS Indicated for use in surgical procedures that require the temporary occlusion of blood flow in a patient s extremities
Stryker Corporation Recall 91849 Information
Status | Ongoing |
Mandated? | Voluntary: Firm initiated |
Recall Number | Z-1340-2023 |
Event ID | 91849 |
Event Description | Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4,1BLA,2PRT QUICK Catalog number: 5921-030-235NS Indicated for use in surgical procedures that require the temporary occlusion of blood flow in a patient s extremities |
Product Type | Devices |
Distribution | US Nationwide distribution. |
Quantity | 1206 units (packs of 10) |
Recall Reason | Not able to achieve desired pressure and not holding pressure result from two different causes which have been reported to occur during initial set-up of the cuff onto the patient, may lead to operative site blood loss, hemorrhage or, in exceedingly rare situations, other major complications |
Device Classification | 20230412 |
Device Code Info | GTIN: 07613327606195 Lot Numbers: 2022111804 2022112902 2022121909 2022121910 2022122603 2022122604 |
Center Classification Date | 20230404 |
Recall Initiation Date | 20230301 |
Recalling Firm | Stryker Corporation |
Initial Notification | Letter |
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