Lower risk Medical device recall · FDA · Published October 9, 2019

Stryker Zimmer Tourniquet Cuff 30" Blue: Mislabeling Risk

Stryker recalls blue 30" Zimmer tourniquet cuffs with potential mislabeling that could cause improper use or inadequate limb compression during procedures.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1802-2020Medical device Stryker ›

Lower-risk recall

Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device misuse during procedure (2) Inadequate Limb Compression Force.

Take action

Contact the company

Recalling firmStryker Sustainability Solutions1810 W Drake Dr · Tempe, AZ 85283-4327

✎ GovInfoNow plain-language explainer

Stryker is recalling blue 30-inch Zimmer tourniquet cuffs that may be mislabeled. This could lead to improper use or insufficient limb compression during medical procedures, risking patient safety. Read more at govinfonow.com/recall/66858-stryker-zimmer-tourniquet-cuff-30-blue-mislabeling-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/66858-stryker-zimmer-tourniquet-cuff-30-blue-mislabeling-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1802-2020

Cite this page

“Stryker Zimmer Tourniquet Cuff 30" Blue: Mislabeling Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/66858-stryker-zimmer-tourniquet-cuff-30-blue-mislabeling-risk. Based on FDA recall #Z-1802-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1802-2020%22&limit=1).

The FDA announced on 2019-10-09 that Stryker Sustainability Solutions is recalling Zimmer Tourniquet Cuff 30" (Blue) PLC Dual Port, Single Bladder units due to potentially mislabeled cuffs. The mislabeling could lead to device misuse during procedures or inadequate limb compression force.

How to tell if you have it

Brand: Stryker
Product: Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder
Item Number: 60-7070-105
UDI: 00885825013868
Lot Number: 10237165

The hazard

The recall involves tourniquet cuffs that are potentially mislabeled. If used, this defect may lead to device misuse during a procedure or inadequate limb compression force.

Context

GovInfoNow's records show Stryker Sustainability Solutions has 22 other recalls on record since 2017-12-01. Recent brand recalls include the Stryker XCEL Bladeless Trocar W/Optiview (2026-08-19) and the Bard EP XT Decapolar Catheter (2026-08-18). Other recent recalls of similar products include Zimmer Sterile Tourniquet Hoses (2026-06-09) and Expressaire Disposable Tourniquet Cuff (2026-08-24).

How to tell if you have this one

Check for the blue color, 30-inch size, PLC Dual Port, Single Bladder, and item number 60-7070-105. The unique device identifier (UDI) 00885825013868 also identifies this specific model.

Brand
Stryker
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the blue color, 30-inch size, PLC Dual Port, Single Bladder, and item number 60-7070-105 on the cuff.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 5 states.

FDA distribution: “US Nationwide distribution including the states of SC, TX, UT, NY, AR” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Arkansas, New York, South Carolina, Texas, Utah.

Recall timeline

FDA terminated this recall 15 months after the firm started it.

Oct 9, 2019Firm started the recall
Apr 27, 2020FDA classified it Class II
May 6, 2020Published in FDA’s Enforcement Report
Jan 14, 2021FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/66858-stryker-zimmer-tourniquet-cuff-30-blue-mislabeling-risk">Stryker Zimmer Tourniquet Cuff 30" Blue: Mislabeling Risk (GovInfoNow)</a>

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-1802-2020 (October 9, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1802-2020 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.