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Stryker GmbH recalls Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-13 (SPI Elast. Sleeve 8-13), Catalog Number 18061407S
Recalled August 11, 2021 · FDA recall Z-2170-2021 · Stryker
Hazard
The devices have a different inner diameter than the diameter specified on the outer box label. · FDA Class II
Units
52
Sold at
US Nationwide Distribution
Description
The devices have a different inner diameter than the diameter specified on the outer box label.
Product
Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-13 (SPI Elast. Sleeve 8-13), Catalog Number 18061407S
Manufacturer(s)
Stryker GmbH
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →