FDA Medical Device Recalls (openFDA)
Stryker Corporation: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4,1 BLA,1PRT QUICK Catalog number: 5921-218-135NS
- Recall number
- Z-1343-2023
- Recalling firm
- Stryker Corporation
- Product
- Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4,1 BLA,1PRT QUICK Catalog number: 5921-218-135NS
- Status
- Open, Classified
- Initiated
- 2023-03-01
- Posted
- 2023-04-04
- Terminated
- not on file
- 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
- Root cause
- Under Investigation by firm
- Action
- Stryker issued Urgent Medical Device Recall letter dated 2/27/23 via 2-day Fedex delivery. The purpose of this letter is to inform you of an increase in reported low pressure events for specific lots of Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuffs and to reiterate the steps in the Instructions For Use (IFU) to mitigate the risk to achieve or maintain pressure. Letter states reason for recall, health risk and action to take: Please review all action steps below and complete the acknowledgement section (pg.3) of this letter and return by email to Instruments.recalls@stryker.com. 1. Immediately review this notification and distribute this letter internally to all users of the Color Cuff Non-Sterile Disposable Tourniquet Cuffs. 2. Follow the subsequent steps from the Instructions For Use (IFU) to mitigate the risk of the cuff not being able to achieve or maintain pressure. Following these steps, you may continue to use the product as-is. a. Prior to using the Non-Sterile Tourniquet Cuffs, please review the Safety Directives, Inspection, and Instructions sections of the IFU. To view this IFU electronically, go to https://ifu.stryker.com/XHR/129532. b. Prior to connecting the Non-Sterile Disposable Tourniquet Cuffs to the Stryker SmartPump, please review the bullet points below from pages 18-20 of the IFU for the SmartPump Tourniquet System. For troubleshooting, please refer to page 28. To view this IFU electronically, go to https://ifu.stryker.com/XHR/129013. " ALWAYS monitor pneumatic connections during use, including the cuff(s) and cuff connector(s) with O-ring, the quick-lock connectors, and the fill line(s) and connectors. If leakage or damage is apparent, see Troubleshooting. " NOTE: If a cuff does not reach or maintain the target pressure value during initial inflation, discontinue using the cuff. See To Switch (or Backup) a Single Cuff. " ALWAYS respond to an alert condition before continuing to use the tourniquet pump. An ALERT symbol, a flashing
- Quantity
- 1730 units (packs of 10)
- Distribution
- US Nationwide distribution.
- Lot, serial or model codes
- GTIN: 07613327606133 Lot Numbers: 2022111801 2022112903 2022121201 2022121202 2022121203 2022121204 2022121205 2022121206
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KCY
- Firm FEI
- 3015967359
- Firm city
- Portage
- Firm state
- MI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28