---
title: "REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R — FDA record Z-2009-2023 | Is It on Recall"
description: "Due to manufacturing issue, their is a potential for peripheral holes to be out of specification."
url: https://isitonrecall.com/recall/fda-device-z-2009-2023-ref-1975-14-500-prima-tt-genoid-monoblock-reverse-tt-baseplate-sterile-r/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R — FDA record Z-2009-2023

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 May 30, 2023. 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**: REF 1975.14.500, Prima TT Genoid Monoblock Reverse TT Baseplate, STERILE R
- **Reason**: Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.
- **Classification**: Class II
- **Recalling firm**: Limacorporate S.p.A
- **Quantity**: 13 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2009-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2009-2023%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 | UDI-DI: 08033390244824; All Lots |

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

## Distribution

US Nationwide distribution in the states of MI, IL, ND, MO, OK.

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**: Jul 5, 2023
- **Recall initiation date**: May 30, 2023
- **Center classification date**: Jun 27, 2023

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-2009-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Limacorporate S.p.A records](https://isitonrecall.com/brand/limacorporate-s-p-a/)
