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Nextremity Solutions recalls Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile. REF: NX-4532K - Product Usage: The Nextra
Recalled March 18, 2020 · FDA recall Z-1458-2020 · Nextremity Solutions
Hazard
Proximal end of the driver in the affected product may be oversized in varying degrees, potentially making it difficult to connect with and remove from the proximal Nextra implant · FDA Class II
Units
190 units
Sold at
International distribution in the countries of Spain, United Kingdom, Germany, and Switzerland.
Description
Proximal end of the driver in the affected product may be oversized in varying degrees, potentially making it difficult to connect with and remove from the proximal Nextra implant
Product
Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile. REF: NX-4532K - Product Usage: The Nextra Hammertoe Correction System is a system of implants and associated instruments which is indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes.
Manufacturer(s)
Nextremity Solutions
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →