DYNANAIL MINI — Class II medical device recall Z-0453-2022
Ongoing recall by Medshape, INC., reported 2022-01-12, distributed in CA, FL, GA, IL, IN, MA, MD, TX…. The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length t
| Recall number | Z-0453-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medshape, INC., Atlanta, GA, United States |
| Recall initiated | 2021-11-17 |
| Classified | 2022-01-04 |
| Reported by FDA | 2022-01-12 |
| Distributed | CA, FL, GA, IL, IN, MA, MD, TX, WA |
| Quantity | 26 units |
| Lot numbers | 04882 |
| Model numbers | 2600-05-006 |
Product
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0453-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.