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Medshape, INC. recalls DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Recalled January 12, 2022 · FDA recall Z-0453-2022 · Medshape
Hazard
The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not seating flush with the nail while inserting during a procedure. · FDA Class II
Units
26 units (1 count)
Sold at
Domestic: CA, FL, GA, IL, IN, MA, MD, TX, and WA.
Description
The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not seating flush with the nail while inserting during a procedure.
Product
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Manufacturer(s)
Medshape, INC.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →