---
title: "Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous De... — FDA record Z-1995-2026 | Is It on Recall"
description: "Includes an incorrect screw seat interface."
url: https://isitonrecall.com/recall/fda-device-z-1995-2026-straumann-n-ce-zr-ht-full-arch-restoration-article-010-0158-endosseous-dental-implant-abutments/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments — FDA record Z-1995-2026

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 Mar 27, 2026. 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**: Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments
- **Reason**: Includes an incorrect screw seat interface.
- **Classification**: Class II
- **Recalling firm**: Straumann USA LLC
- **Quantity**: 6 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1995-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1995-2026%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 | Article 010.0158. UDI: (01)07630031759764(11)YYMMDD(10)XXXXX. Project Numbers: 28000US\_00622\_00\_b00, 28000US\_00431\_00\_b00, 28000US\_00489\_00\_b00, 28000US\_00792\_00\_b00, 28000US\_00908\_00\_b00, 28000US\_00908\_01\_b00. |

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

## Distribution

US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.

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

- [Alabama](https://isitonrecall.com/state/alabama/)
- [Arizona](https://isitonrecall.com/state/arizona/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Hawaii](https://isitonrecall.com/state/hawaii/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: May 6, 2026
- **Recall initiation date**: Mar 27, 2026
- **Center classification date**: Apr 29, 2026

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-1995-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Straumann USA LLC records](https://isitonrecall.com/brand/straumann-usa-llc/)