Stryker, Inc. FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. Matched by name to SYK.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cmClass IIDec 6, 2023The microcatheter IFU contains an intended use that has not	The microcatheter IFU contains an intended use that has not been evaluated by the FDA.	Class IIDevices	Dec 6, 2023
Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cmClass IIDec 6, 2023The microcatheter IFU contains an intended use that has not	The microcatheter IFU contains an intended use that has not been evaluated by the FDA.	Class IIDevices	Dec 6, 2023