---
title: "Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 0... — FDA record Z-1632-2026 | Is It on Recall"
description: "A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot"
url: https://isitonrecall.com/recall/fda-device-z-1632-2026-custom-abutment-ti-for-straumann-rc-incl-tan-screw-catalog-number-art-027-4620/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620; — FDA record Z-1632-2026

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 17, 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**: Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;
- **Reason**: A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorrectly identified as a Titanium Bar Ti Gr4 D (SAP #701922 / Lot 7130430). As a result, RC Titanium abutments were manufactured using the TAN Bar material on Mill-from-Bar Machine 396-06.
- **Classification**: Class II
- **Recalling firm**: Straumann USA LLC
- **Quantity**: 13 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1632-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1632-2026%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 | Catalog Number/Art.: 027.4620; UDI-DI: 07630031713766; Order number (lot): 92465US\_12039\_00\_b00 , 92465US\_12040\_00\_b00 , 92465US\_12047\_00\_b00 , 92465US\_12048\_00\_b00 , 70959US\_02227\_00\_b00 , 94021US\_02348\_00\_b00, 70416US\_07543\_00\_b00 , 91395US\_01687\_00\_b00 , 91545US\_03284\_00\_b00 , 91545US\_03285\_00\_b00 , 71711US\_00420\_00\_b00 , 91853US\_06313\_00\_b00 , 72747US\_00247\_00\_b00; |

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

## Distribution

Worldwide - US Nationwide distribution in the states of CA, CO, FL, IA, IL, MN, MO, MT, OR, WA; and the country of Canada.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Apr 1, 2026
- **Recall initiation date**: Mar 17, 2026
- **Center classification date**: Mar 24, 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-1632-2026%22)

## Related records

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