Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SurgiCount+ Software Application-indicated as an adjunctive technology for augmenting the Recalled by Stryker Corporation Due to Potential for current software to miscount when scanning...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Corporation directly.
Affected Products
SurgiCount+ Software Application-indicated as an adjunctive technology for augmenting the manual process of counting, displaying and recording the number of RFID-tagged absorbent articles used during surgical procedures Product Code: 0694-002-090;
Quantity: 57 units
Why Was This Recalled?
Potential for current software to miscount when scanning in multiple sponge-products from the same unique sponge-pack type
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Corporation
Stryker Corporation has 108 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report