Stryker Neurovascular: 68 recalls on record

Recalls filed with 1 agency: FDA (68).

First recall on record: July 31, 2013. Most recent: July 1, 2026.

Risk classification: Class II: 68

Most recent recalls

DateAgencyProduct
July 1, 2026FDAINZONE DETACHMENT SYSTEM, REF: M00345100950Z-2552-2026
October 16, 2024FDAThe Trevo Trak 21 Microcatheter is a single-lumen, braided shaft, variable stiffness cath…Z-0021-2025
June 12, 2024FDAThe Synchro SELECT Guidewires are a steerable guidewire family with a shapeable tip and …Z-1940-2024
June 12, 2024FDAThe Synchro Neuro Guidewires are a steerable guidewire family with a shapeable tip. The o…Z-1939-2024
June 12, 2024FDAThe Synchro2 Guidewires are a steerable guidewire family with a shapeable tip and are ava…Z-1941-2024
June 5, 2024FDAFlowGate2 8F x 85cm, Catalog: 90485 FlowGate2 8F x 95cm, Catalog: 90495Z-1907-2024
June 5, 2024FDATrevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catal…Z-1902-2024
June 5, 2024FDATrevo ProVue, Catalog: 90184Z-1903-2024
June 5, 2024FDATrevo Pro 14 Microcatheter, Catalog: 90231; Trevo Pro 18 Microcatheter, Catalog: 90238Z-1904-2024
June 5, 2024FDASynchro .014"guide wire, 35 cm tip, Catalog: M00313010 Synchro .014 guide wire, 300 cm l…Z-1909-2024
June 5, 2024FDADAC 044 115cm, Catalog: 90760Z-1908-2024
June 5, 2024FDATrevo Trak 21 Microcatheter, Catalog: 90338Z-1906-2024
June 5, 2024FDATrevo NXT ProVue 3 x 32, US, Catalog: 90312 Kits: TREVO NXT 3X32+TRAK21 2-PACK - CE, …Z-1905-2024
May 8, 2024FDAThe Distal Access Catheter is a single-lumen, braided shaft, variable stiffness catheter …Z-1740-2024
November 6, 2019FDASynchro2, 0.014in x 200cm STANDARD Guidewire with Hydrophilic Coating, UPN Product No. M0…Z-0229-2020
November 6, 2019FDASynchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M003…Z-0225-2020
August 8, 2018FDAFlowGate2 Balloon Guide Catheter, UPN 90485 (8Fx85cm size) and 90495 (8Fx95cm size)Z-2569-2018
January 24, 2018FDATrevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo P…Z-0347-2018
December 27, 2017FDAStroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 6 mm, 25 mm; Excelsior…Z-0275-2018
December 27, 2017FDATrevo(TM) XP ProVue Procedure Pack, TREVO(TM) XP PROVUE RETRIEVER, 6 mm, 25 mm, .Excelsio…Z-0277-2018
December 27, 2017FDAStroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 4 mm, 20 mm, ; Trevo(T…Z-0276-2018
August 9, 2017FDAStroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20, Trevo Pro 14 Microcatheter, AXS Ca…Z-2799-2017
August 9, 2017FDAStroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS …Z-2800-2017
August 9, 2017FDAStroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30, Trevo Pro 18 Microcatheter, AXS …Z-2801-2017
November 9, 2016FDAGuider Softip XF; GUIDER/MP XF/6FR/90CM, Model number: H965100460. Cardiology: Bost…Z-0336-2017

Questions about this company

How many recalls does Stryker Neurovascular have?
Recalert has 68 U.S. recalls on record for Stryker Neurovascular, published between July 31, 2013 and July 1, 2026.
What was the most recent Stryker Neurovascular recall?
FDA recall Z-2552-2026, published July 1, 2026: INZONE DETACHMENT SYSTEM, REF: M00345100950
Which agencies have handled Stryker Neurovascular recalls?
Stryker Neurovascular appears as the recalling firm in recalls from: FDA (68).

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