---
title: "NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R — FDA record Z-0658-2022 | Is It on Recall"
description: "Due to 16 complaints related to drivers not engaging in implants. According to the firm's investigations, the incorrect offset gauge was potentially used during"
url: https://isitonrecall.com/recall/fda-device-z-0658-2022-nobelreplace-conical-connection-rp-4-3x11-5-mm-ref-36707-sterile-r/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R — FDA record Z-0658-2022

Reported terminated

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 Dec 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**: NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R
- **Reason**: Due to 16 complaints related to drivers not engaging in implants. According to the firm's investigations, the incorrect offset gauge was potentially used during production of the implants. As a result, this could potentially lead to aborted or a delay in surgical procedure.
- **Classification**: Class II
- **Recalling firm**: Nobel Biocare Usa Llc
- **Quantity**: 702 pieces
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0658-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0658-2022%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 | Catalog Number: 36707 UDI Code: (01)07332747160529(10)13116495(11)210720(17)260618; (01)07332747160529(10)13116496(11)210720(17)260618; (01)07332747160529(10)13116497(11)210720(17)260618; Lot Numbers: 13116495, 13116496, 13116497 |

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

## Distribution

Worldwide distribution - U.S. Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, MA, ME, MI, MN, MS, NC, NJ, NM, NV, NY, OH, OR, PA, SC, TN, TX, UT, VA, VT, WA and WI. The countries of Canada, Mexico and Turkey.

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

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## Dates in the source

- **Report date**: Mar 2, 2022
- **Recall initiation date**: Dec 17, 2021
- **Center classification date**: Feb 18, 2022
- **Termination date**: Oct 25, 2024

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-0658-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Nobel Biocare Usa Llc records](https://isitonrecall.com/brand/nobel-biocare-usa-llc/)
