---
title: "Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST — FDA record Z-0334-2023 | Is It on Recall"
description: "An internal technical investigation has confirmed that Thermo Scientific\" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Prote"
url: https://isitonrecall.com/recall/fda-device-z-0334-2023-thermo-scientific-sensititre-stp6f-gram-negative-ivd-ast/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST — FDA record Z-0334-2023

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 Oct 20, 2022. 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**: Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST
- **Reason**: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
- **Classification**: Class I
- **Recalling firm**: Remel Inc
- **Quantity**: 2656 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0334-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0334-2023%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 | Lot Numbers: B2314, B2174, B2036, B1346, B1183, B1115, B1027 |

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

## Distribution

US Nationwide Distribution

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**: Dec 14, 2022
- **Recall initiation date**: Oct 20, 2022
- **Center classification date**: Dec 7, 2022
- **Termination date**: Sep 30, 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-0334-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Remel Inc records](https://isitonrecall.com/brand/remel-inc/)
