--- title: "Stryker Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Stryker Corporation 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-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Stryker Corporation recall records **85** reported ongoing 95 records in this archive. Latest source date Jun 8, 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 Jun 8, 2026 FDA device enforcement ### [STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600](https://isitonrecall.com/recall/fda-device-z-2862-2026-stryker-ahto-tube-set-packaging-catalog-number-0250070600/) There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, S... [Official source for STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2862-2026%22) Jun 8, 2026 FDA device enforcement ### [STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620](https://isitonrecall.com/recall/fda-device-z-2863-2026-stryker-ahto-tube-set-with-tip-packaging-catalog-number-0250070620/) There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, S... [Official source for STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2863-2026%22) Jun 8, 2026 FDA device enforcement ### [STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640](https://isitonrecall.com/recall/fda-device-z-2864-2026-stryker-ahto-dual-spike-tube-set-packaging-catalog-number-0250070640/) There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, S... [Official source for STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2864-2026%22) Jun 8, 2026 FDA device enforcement ### [STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530](https://isitonrecall.com/recall/fda-device-z-2865-2026-stryker-pkg-single-spike-tube-set-catalog-number-0250070530/) There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, S... [Official source for STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2865-2026%22) Jun 8, 2026 FDA device enforcement ### [STRYKER PKG., STRYKEFLOW SUCTION/IRRIGATOR PS, Catalog Number 0250070540](https://isitonrecall.com/recall/fda-device-z-2866-2026-stryker-pkg-strykeflow-suction-irrigator-ps-catalog-number-0250070540/) There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Chile, France, Germany, Indonesia, Italy, Mexico, Netherlands, New Zealand, Philippines, S... [Official source for STRYKER PKG., STRYKEFLOW SUCTION/IRRIGATOR PS, Catalog Number 0250070540](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2866-2026%22) May 6, 2026 FDA device enforcement ### [Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System](https://isitonrecall.com/recall/fda-device-z-2282-2026-neptune-smart-docking-station-120v-catalog-number-0770-100-000-part-of-the-neptune-waste-management/) It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to th... Class II Reported ongoing Distribution: US Nationwide distribution in the state of Indiana. [Official source for Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Mana...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2282-2026%22) Apr 9, 2026 FDA device enforcement ### [Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the FluidSmart Fluid Management System, which i...](https://isitonrecall.com/recall/fda-device-z-2166-2026-thermedx-fluidsmart-urology-tube-set-ref-ll0006-udi-di-code-00860936000365-the-fluidsmart-tube-sets/) Due to nonconforming products being inadvertently distributed. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the state of GA. [Official source for Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube S...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2166-2026%22) Jan 21, 2026 FDA device enforcement ### [MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN): 00850024195028 MS-00009 (Pack of 10) - MOLLI Introducer (12cm, 14G...](https://isitonrecall.com/recall/fda-device-z-1427-2026-molli-2-system-system-includes-mm1000-pack-of-10-molli-introducer-8cm-14g-and-molli-marker-udi-gtin/) Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AL, AK, AZ, AR, CA, CO, CT, DC, FL, GA, HI ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH... [Official source for MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marke...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1427-2026%22) Oct 31, 2025 FDA device enforcement ### [NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAA...](https://isitonrecall.com/recall/fda-device-z-0599-2026-nico-myriad-handpiece-product-number-product-name-nn-8000-15x10-mhp-nn-8001-15x-13-mhp-nn-8002-15x-2/) Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, England, Ireland, Italy, Kuwait, Singapore, Slovenia, Spain, and the Netherlands. [Official source for NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0599-2026%22) Oct 31, 2025 FDA device enforcement ### [NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber](https://isitonrecall.com/recall/fda-device-z-0600-2026-nico-myriad-illumination-pack-product-no-nn-1000-11g-illumination-sleeve-fiber-product-no-nn-1001-13/) Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, England, Ireland, Italy, Kuwait, Singapore, Slovenia, Spain, and the Netherlands. [Official source for NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0600-2026%22) Oct 31, 2025 FDA device enforcement ### [NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde;...](https://isitonrecall.com/recall/fda-device-z-0601-2026-nico-brainpath-product-number-product-name-nn-8024-brainpath-shephard-s-hook-greenberg-nn-8025-brain/) Tape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Canada, England, Ireland, Italy, Kuwait, Singapore, Slovenia, Spain, and the Netherlands. [Official source for NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-802...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0601-2026%22) Jul 2, 2025 FDA device enforcement ### [Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-018-135; DISP 18X3,1BLA,2PRT QUICK / 5921-018-235; DISP 24X4,1BLA, 2PRT QUICK / 59...](https://isitonrecall.com/recall/fda-device-z-2277-2025-stryker-smartpump-tourniquet-disposable-sterile-single-use-disp-18x3-1bla-1prt-quick-5921-018-135-di/) 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 hypotension and cardiovascular collapse an... Class II Reported ongoing Distribution: Domestic US distribution nationwide. International distribution to Australia Canada Hong Kong India Malaysia Netherlands New Zealand Singapore Sweden Thailand United Kingdom [Official source for Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-01...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2277-2025%22) Jun 18, 2025 FDA device enforcement ### [Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip](https://isitonrecall.com/recall/fda-device-z-2170-2025-stryker-strykeflow-ref-0250070500-2-disposable-suction-irrigator-without-disposable-tip/) Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida,... [Official source for Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2170-2025%22) Jun 18, 2025 FDA device enforcement ### [Stryker, StrykeFlow REF: 0250070520 / 2, Disposable Suction/Irrigator with Disposable Tip](https://isitonrecall.com/recall/fda-device-z-2171-2025-stryker-strykeflow-ref-0250070520-2-disposable-suction-irrigator-with-disposable-tip/) Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida,... [Official source for Stryker, StrykeFlow REF: 0250070520 / 2, Disposable Suction/Irrigator with Disposable Tip](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2171-2025%22) Feb 25, 2025 FDA device enforcement ### [Otopore Cylinder Standard outer ear dressings, Catalog Numbers 5400-010-000 and 5400-010-000ITL](https://isitonrecall.com/recall/fda-device-z-1469-2025-otopore-cylinder-standard-outer-ear-dressings-catalog-numbers-5400-010-000-and-5400-010-000itl/) There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Otopore Cylinder Standard outer ear dressings, Catalog Numbers 5400-010-000 and 5400-010-000ITL](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1469-2025%22) Feb 25, 2025 FDA device enforcement ### [Nasopore Standard 4cm fragmentable nasal dressing, Catalog Numbers 5400-010-004 and 5400-010-004ITL](https://isitonrecall.com/recall/fda-device-z-1470-2025-nasopore-standard-4cm-fragmentable-nasal-dressing-catalog-numbers-5400-010-004-and-5400-010-004itl/) There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Nasopore Standard 4cm fragmentable nasal dressing, Catalog Numbers 5400-010-004 and 5400-010-004ITL](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1470-2025%22) Feb 25, 2025 FDA device enforcement ### [Nasopore Standard 8cm fragmentable nasal dressing, Catalog Numbers 5400-010-008 and 5400-010-008ITL](https://isitonrecall.com/recall/fda-device-z-1471-2025-nasopore-standard-8cm-fragmentable-nasal-dressing-catalog-numbers-5400-010-008-and-5400-010-008itl/) There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Nasopore Standard 8cm fragmentable nasal dressing, Catalog Numbers 5400-010-008 and 5400-010-008ITL](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1471-2025%22) Feb 25, 2025 FDA device enforcement ### [Otopore Cylinder outer ear wound dressing, Firm Catalog Number 5400-020-000 and Forte Catalog Number 5400-020-000TL](https://isitonrecall.com/recall/fda-device-z-1472-2025-otopore-cylinder-outer-ear-wound-dressing-firm-catalog-number-5400-020-000-and-forte-catalog-number/) There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Otopore Cylinder outer ear wound dressing, Firm Catalog Number 5400-020-000 and Forte Catalog Num...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1472-2025%22) Feb 25, 2025 FDA device enforcement ### [Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITL](https://isitonrecall.com/recall/fda-device-z-1473-2025-nasopore-8cm-fragmentable-nasal-dressing-firm-catalog-number-5400-020-008-and-forte-catalog-number-5/) There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Numb...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1473-2025%22) Feb 25, 2025 FDA device enforcement ### [Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL](https://isitonrecall.com/recall/fda-device-z-1474-2025-nasopore-4cm-fragmentable-nasal-dressing-firm-catalog-number-5400-020-004-and-forte-catalog-number-5/) There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Numb...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1474-2025%22) ## Reasons in these listed records - There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use. - It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety te... - Due to nonconforming products being inadvertently distributed. - Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue removal procedures. These examples come from this result page and are not a ranking of every recall reason. ## Checking Stryker Corporation ### Is there a recall on stryker corporation right now? This archive contains 95 records, including 85 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 Corporation](https://isitonrecall.com/check/?q=Stryker%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)