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Stryker Corporation recalls SurgiCount+ Software Application-indicated as an adjunctive technology for augmenting the manual process of counting, di
Recalled September 6, 2023 · FDA recall Z-2463-2023 · Stryker
Hazard
Potential for current software to miscount when scanning in multiple sponge-products from the same unique sponge-pack type · FDA Class II
Units
57 units
Sold at
US Nationwide distribution.
Description
Potential for current software to miscount when scanning in multiple sponge-products from the same unique sponge-pack type
Product
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;
Manufacturer(s)
Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →