Reported Jan 12, 2022 · Ongoing
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Medshape, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medshape, INC. · 1575 Northside Dr Nw Ste 440 · Atlanta, GA · 30318-4211
Is this the product you have?
- DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
- Lot codes and dates
Model No. 2600-05-006Lot No. 04882
- UDIM97026000500060
- Amount recalled
- 26 units (1 count)
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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