Stryker Corporation recalls Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-018-135; DISP 18X3,1BLA,2PRT QUICK /…
Tourniquet cuff flange may become detached from the bladder. If leak occurs during the procedure, there may be risk of hemorrhage, resulting in blood loss greater than expected. Other serious risks include cerebral…
Read the official notice →- Date
- 2025-08-13
- Country
- United States
- Brand
- Stryker
- Product
- Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-018-135; DISP 18X3,1BLA,2PRT QUICK /…
- Classification
- Class II
- Units
- Domestic US distribution nationwide. International distribution to Australia…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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FDA · DeviceStryker CorporationWorldwide - U.S. Nationwide distribution including in the states of AL, AK,…Official notice → - 2025-12-03
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FDA · DeviceStryker CorporationWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - 2025-07-30
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Other drugs & medical recalls in the United States
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Glenmark Pharmaceuticals Inc., USA recalls Carvedilol Tablets, USP, 12.5 mg, 500-count bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd, Colvale-Bardez,…
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Ascend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/ 40 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA;…
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Intersurgical Inc recalls One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.
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FDA · DeviceIntersurgical IncUS distribution to AZ, CA, CT, FL, FL, HI, MA, MI, OH, UT, VA.Official notice → - US
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