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Stryker Spine recalls LITe Decompression Snake Arm, REF 48080230
Recalled December 27, 2023 · FDA recall Z-0610-2024 · Stryker Spine
Hazard
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft. · FDA Class II
Units
9
Sold at
US: MD, MI, NM, TX & OUS: Canada & France.
Description
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Product
LITe Decompression Snake Arm, REF 48080230
Manufacturer(s)
Stryker Spine
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →