Stryker Tourniquet Cuff 30" Blue: Mislabeling Risk
Stryker recalls blue 30" tourniquet cuffs labeled as dual port but contain single port. Check packaging for model number 60-7070-0:005 to avoid confusion.
Lower-risk recall
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
Contact the company
What happened, in plain English
Stryker is recalling blue 30-inch tourniquet cuffs that were mislabeled as having dual ports but actually have single ports. This could lead to confusion during medical use, though it does not pose a safety risk. Read more at govinfonow.com/recall/54953-stryker-tourniquet-cuff-30-blue-mislabeling-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/54953-stryker-tourniquet-cuff-30-blue-mislabeling-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2405-2024
Cite this page
“Stryker Tourniquet Cuff 30" Blue: Mislabeling Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54953-stryker-tourniquet-cuff-30-blue-mislabeling-risk. Based on FDA recall #Z-2405-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2405-2024%22&limit=1).
Why it’s dangerous
The tourniquet cuffs were labeled as having dual ports and single bladder but actually contain single ports and single bladder. This mislabeling could cause confusion during medical procedures, but it does not pose a safety risk.
Who’s affected
Healthcare professionals using these tourniquet cuffs for medical procedures may be affected. Patients receiving care with these cuffs could also be impacted.
How to tell if you have this one
Check for the model number 60-7070-005 on the packaging. The product is blue, 30 inches long, and labeled as Luer-Lock Dual Port, single Bladder, RxOnly.
- Brand
Stryker- Category
Medical device
What to do — step by step
Check Product Label
Look for the model number 60-7070-005 on the packaging to confirm it is the recalled item.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 6 states.
FDA distribution: “US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Colorado, Illinois, Michigan, Oregon, Wisconsin.
Recall timeline
FDA published this recall 54 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using this product?
No, the mislabeling does not require stopping use. The product is safe but may need to be re-labeled for clarity.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2405-2024 (May 31, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2405-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.