---
title: "T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL — FDA record Z-2707-2026 | Is It on Recall"
description: "Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility."
url: https://isitonrecall.com/recall/fda-device-z-2707-2026-t-lok-bone-marrow-tray-ref-bmt1104stl-bmet1104tl-bmt1104catl/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL — FDA record Z-2707-2026

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 Jun 1, 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**: T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL
- **Reason**: Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
- **Classification**: Class I
- **Recalling firm**: Argon Medical Devices, Inc
- **Quantity**: 850
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2707-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2707-2026%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 | REF/UDI-DI Box:Unit/Lot(Expiration): BMT1104STL/20886333007862:00886333007868/11650679(11/30/2026); BMET1104TL/20886333007602:00886333007608/11654764(3/31/2028); BMT1104CATL/20886333007763:00886333007769/11650887(11/30/2026) |

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

## Distribution

Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago.

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

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- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
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- [South Dakota](https://isitonrecall.com/state/south-dakota/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jul 22, 2026
- **Recall initiation date**: Jun 1, 2026
- **Center classification date**: Jul 10, 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-2707-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Argon Medical Devices, Inc records](https://isitonrecall.com/brand/argon-medical-devices-inc/)
