---
title: "DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile — FDA record Z-0453-2022 | Is It on Recall"
description: "The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introduci"
url: https://isitonrecall.com/recall/fda-device-z-0453-2022-dynanail-mini-endcap-6mm-ref-2600-05-006-rx-only-sterile/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile — FDA record Z-0453-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 17, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: Medshape, INC.
- **Quantity**: 26 units (1 count)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0453-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0453-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model No. 2600-05-006; Lot No. 04882; UDI: M97026000500060 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic: CA, FL, GA, IL, IN, MA, MD, TX, and WA.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Jan 12, 2022
- **Recall initiation date**: Nov 17, 2021
- **Center classification date**: Jan 4, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0453-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medshape, INC. records](https://isitonrecall.com/brand/medshape-inc/)