Lower risk Medical device recall · FDA · Published July 25, 2019

Stry: Endotrig ETF Hook Blade Recall - Sterile Bag Seal Risk

Stryker recalls Endotrig ETF Hook Blade (Catalog 1052-1) due to potential compromised sterile bag seals. This could risk infection during surgery. Affected lots: 01406, 01475.

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

🇺🇸 FDA recall #Z-2412-2019Medical device Stryker ›

Lower-risk recall

The seal integrity of the sterile bag containing the kits may be compromised.

Take action

Contact the company

Recalling firmStryker GmbHBohnackerweg 1 · Selzach, Switzerland

✎ GovInfoNow plain-language explainer

Stryker is recalling Endotrig ETF Hook Blade surgical kits because the sterile packaging might not stay sealed properly. This could lead to infections if the kit is used without a clean seal. Read more at govinfonow.com/recall/67323-stry-endotrig-etf-hook-blade-recall-sterile-bag-seal-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/67323-stry-endotrig-etf-hook-blade-recall-sterile-bag-seal-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2412-2019

Cite this page

“Stry: Endotrig ETF Hook Blade Recall - Sterile Bag Seal Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67323-stry-endotrig-etf-hook-blade-recall-sterile-bag-seal-risk. Based on FDA recall #Z-2412-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2412-2019%22&limit=1).

The FDA announced on July 25, 2019, that Stryker GmbH voluntarily recalled Endotrig ETF Hook Blade kits due to compromised sterile bag seal integrity. The agency issued recall number Z-2412-2019 for the Class II device distributed nationwide in the United States.

How to tell if you have it

Brand: Stryker
Product: Endotrig ETF Hook Blade
Catalog Number: 1052-1
Lot Numbers: 01406, 01475

The hazard

The FDA stated that the seal integrity of the sterile bag containing the kits may be compromised. The EPF system is designed for the treatment of plantar fasciosis.

Context

GovInfoNow's records show Stryker GmbH has 20 other recalls on record since March 12, 2018. Recent brand recalls include the Stryker Hoffmann II Connecting Rod Micro 3 x 120mm (July 1, 2026) and the Stryker Gamma4 Right Long Nail (May 28, 2025). Other recent recalls of similar products include the Stryker BARD EP XT Decapolar Steerable Catheter (April 10, 2026), the Stryker BARD EP XT Steerable Catheter (April 10, 2026), and the Stryker Daig Livewire Steerable Catheter (April 10, 2026).

How to tell if you have this one

Check the lot number on the packaging. The affected items have lot numbers 01406 or 01475. The product is the Endotrig ETF Hook Blade with catalog number 1052-1.

Brand
Stryker
Category
Medical device

FDA recall event · 13 products

All 13 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Terminated
Distribution
US Nationwide Distribution

Recall number	Product, codes & lots	Quantity
Z-2412-2019	Endotrig ETF Hook Blade, Catalog Number 1052-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Numbers 01406, 01475	35
Z-2413-2019	Endotrac ECTR Push Blade, Catalog Number 2053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Number 01400	476
Z-2414-2019	Endotrac ECTR Triangle Blade, Catalog Number 2054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Number 01407	53
Z-2415-2019	Endotrac ECTR Hook Blade, Catalog Number 2055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Numbers 01409, 01476	1959
Z-2416-2019	Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Numbers 01399, 01464, 01477	251
Z-2417-2019	Endotrac EPF/EGR Triangle Blade, Catalog Number 3054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Numbers 01398, 01465, 01481	1533
Z-2418-2019	Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Numbers 01403, 01466, 01483	2248
Z-2419-2019	Endintrak 2 Hook Blade, Catalog Number 4058-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Number 01412	76
Z-2420-2019	Endotrac ECTR Triangle Blade, Angled, Catalog Number 2054A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Number 01408	94
Z-2421-2019	Endotrac ECTR Hook Blade, Angled, Catalog Number 2055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Number 01401	28
Z-2422-2019	Endotrac EPF/EGR Triangle Blade, Angled, Catalog Number 3054A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Number 01411	21
Z-2423-2019	Endotrac EPF/EGR Hook Blade, Angled, Catalog Number 3055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Number 01402	110
Z-2424-2019	Endintrak¿ 2 Hook Blade, Angled, Catalog Number 4058A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.; Lot Number 01405, 01479	259

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for lot numbers 01406 or 01475 on the packaging.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “US Nationwide Distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

Jul 25, 2019Firm started the recall
Aug 27, 2019FDA classified it Class II
Sep 4, 2019Published in FDA’s Enforcement Report
Sep 24, 2020FDA terminated the recall

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

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Is there a risk of serious injury?

The recall is for potential infection risk, not direct injury. The hazard does not involve death or serious injury in normal use.

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Link to this recall

<a href="https://govinfonow.com/recall/67323-stry-endotrig-etf-hook-blade-recall-sterile-bag-seal-risk">Stry: Endotrig ETF Hook Blade Recall - Sterile Bag Seal 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-2412-2019 (July 25, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2412-2019 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.