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All product recalls associated with Stryker, Inc..
Total Recalls
3
Past Year
0
Class I (Serious)
0
Most Recent
Dec 2023
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
On 06/09/2009, Stryker Sustain ability Solutions, formerly Ascent Healthcare Solutions, recalled lots 674201 & 674290 of their Reprocessed Mitek Arthroscopic Wand due to the lots not being tested in accordance with the functional test requirement during the time frame of 04/14/09 to 05/25/09.