--- title: "Stryker Sustainability Solutions Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Stryker Sustainability Solutions recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/stryker-sustainability-solutions/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Stryker Sustainability Solutions recall records **40** reported ongoing 41 records in this archive. Latest source date Aug 19, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 19, 2026 FDA device enforcement ### [REF:2B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 100MM](https://isitonrecall.com/recall/fda-device-z-3182-2026-ref-2b5lt-ethicon-endo-surgery-inc-xcel-bladeless-trocar-w-optiview-technology-sleeve-5mm-x-100mm/) Reusable access port system may crack or seperate during use. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, ... [Official source for REF:2B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3182-2026%22) Aug 19, 2026 FDA device enforcement ### [REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM](https://isitonrecall.com/recall/fda-device-z-3183-2026-ref-2b5st-ethicon-endo-surgery-inc-xcel-bladeless-trocar-w-optiview-technology-sleeve-5mm-x-75mm/) Reusable access port system may crack or seperate during use. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, ... [Official source for REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3183-2026%22) Aug 19, 2026 FDA device enforcement ### [REF:B11LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 11X100MM](https://isitonrecall.com/recall/fda-device-z-3184-2026-ref-b11lt-ethicon-endo-surgery-inc-xcel-bladeless-trocar-w-stability-sleeve-11x100mm/) Reusable access port system may crack or seperate during use. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, ... [Official source for REF:B11LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 11X100MM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3184-2026%22) Aug 19, 2026 FDA device enforcement ### [REF:B12LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 12X100MM](https://isitonrecall.com/recall/fda-device-z-3185-2026-ref-b12lt-ethicon-endo-surgery-inc-xcel-bladeless-trocar-w-stability-sleeve-12x100mm/) Reusable access port system may crack or seperate during use. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, ... [Official source for REF:B12LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 12X100MM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3185-2026%22) Aug 19, 2026 FDA device enforcement ### [REF:B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 5X100MM](https://isitonrecall.com/recall/fda-device-z-3186-2026-ref-b5lt-ethicon-endo-surgery-inc-xcel-bladeless-trocar-w-stability-sleeve-5x100mm/) Reusable access port system may crack or seperate during use. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, ... [Official source for REF:B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 5X100MM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3186-2026%22) Aug 19, 2026 FDA device enforcement ### [REF:B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 5X75MM](https://isitonrecall.com/recall/fda-device-z-3187-2026-ref-b5st-ethicon-endo-surgery-inc-xcel-bladeless-trocar-w-stability-sleeve-5x75mm/) Reusable access port system may crack or seperate during use. Class II Reported ongoing Distribution: US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, ... [Official source for REF:B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY SLEEVE 5X75MM](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3187-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2174-2026-bard-dynamic-deca-steerable-product-number-201101-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2174-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2175-2026-bard-dynamic-tip-steerable-product-number-200131-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2175-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2176-2026-bard-dynamic-tip-steerable-product-number-200344-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2176-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD Dynamic Tip Steerable, Product Number 6DYNTP001;](https://isitonrecall.com/recall/fda-device-z-2177-2026-bard-dynamic-tip-steerable-product-number-6dyntp001/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD Dynamic Tip Steerable, Product Number 6DYNTP001;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2177-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2178-2026-bard-dynamic-xt-deca-steerable-product-number-201102-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2178-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2179-2026-bard-dynamic-xt-steerable-product-number-201103-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2179-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2180-2026-bard-dynamic-xt-steerable-product-number-201104-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2180-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2181-2026-bard-ep-xt-decapolar-steerable-product-number-201007-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2181-2026%22) Apr 10, 2026 FDA device enforcement ### [BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2182-2026-bard-ep-xt-steerable-product-number-200794-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2182-2026%22) Apr 10, 2026 FDA device enforcement ### [BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2183-2026-bw-webster-duo-decapolar-product-number-d728260rt-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2183-2026%22) Apr 10, 2026 FDA device enforcement ### [CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2184-2026-cs-uni-directional-w-auto-id-product-number-d135303-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2184-2026%22) Apr 10, 2026 FDA device enforcement ### [CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2185-2026-cs-uni-directional-w-auto-id-product-number-d135304-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2185-2026%22) Apr 10, 2026 FDA device enforcement ### [Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2186-2026-daig-livewire-steerable-product-number-401575-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2186-2026%22) Apr 10, 2026 FDA device enforcement ### [Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://isitonrecall.com/recall/fda-device-z-2187-2026-daig-livewire-steerable-product-number-401581-reprocessed-electrophysiology-catheter/) Incomplete seals on sterile product Class II Reported ongoing Distribution: US Nationwide and the countries of Israel and Canada. [Official source for Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2187-2026%22) ## Reasons in these listed records - Reusable access port system may crack or seperate during use. - Incomplete seals on sterile product These examples come from this result page and are not a ranking of every recall reason. ## Checking Stryker Sustainability Solutions ### Is there a recall on stryker sustainability solutions right now? This archive contains 41 records, including 40 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Stryker Sustainability Solutions](https://isitonrecall.com/check/?q=Stryker%20Sustainability%20Solutions) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)