---
title: "Hamilton-T1, REF: 161006, Intensive Care and Transport Ventilator — FDA record Z-2526-2023 | Is It on Recall"
description: "Degrading capacitors on the control board of ventilators and spare parts may leak electrolyte onto the control board causing a short circuit on the board and/or"
url: https://isitonrecall.com/recall/fda-device-z-2526-2023-hamilton-t1-ref-161006-intensive-care-and-transport-ventilator/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Hamilton-T1, REF: 161006, Intensive Care and Transport Ventilator — FDA record Z-2526-2023

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 Jul 26, 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**: Hamilton-T1, REF: 161006, Intensive Care and Transport Ventilator
- **Reason**: Degrading capacitors on the control board of ventilators and spare parts may leak electrolyte onto the control board causing a short circuit on the board and/or the capacitor to lose function and lead to interruption of ventilation.
- **Classification**: Class I
- **Recalling firm**: Hamilton Medical, Inc.
- **Quantity**: 76 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2526-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2526-2023%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: 07630002801850 & 07630002813532 / Affected Serial Numbers: 15929 17600 17661 17677 17698 17699 17741 17850 17877 17913 17925 17955 17957 17969 17975 17976 17982 17985 17986 17991 17993 17995 18009 18166 18183 18189 18191 18199 18224 18244 18251 18255 18256 18260 18263 18272 18273 18276 18288 18289 18305 18308 18333 18340 18349 18360 18363 18377 18378 18383 18414 18415 18419 18441 18451 18458 18461 18502 18537 18544 18550 18778 18784 19237 19290 19291 19292 19293 19294 19298 19304 19305 19470 19483 19490 26117 |

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

## Distribution

Distribution US nationwide, including Puerto Rico. OUS: Not provided

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**: Sep 27, 2023
- **Recall initiation date**: Jul 26, 2023
- **Center classification date**: Sep 20, 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-2526-2023%22)

## Related records

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