---
title: "Masimo LNOP TC-I SpO2, Reusable Ear Sensor, REF: 1794 — FDA record Z-1984-2023 | Is It on Recall"
description: "TC-I tip clip sensor may produce readings outside the accuracy specification."
url: https://isitonrecall.com/recall/fda-device-z-1984-2023-masimo-lnop-tc-i-spo2-reusable-ear-sensor-ref-1794/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Masimo LNOP TC-I SpO2, Reusable Ear Sensor, REF: 1794 — FDA record Z-1984-2023

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 Apr 21, 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**: Masimo LNOP TC-I SpO2, Reusable Ear Sensor, REF: 1794
- **Reason**: TC-I tip clip sensor may produce readings outside the accuracy specification.
- **Classification**: Class II
- **Recalling firm**: Masimo Corporation
- **Quantity**: 86 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1984-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1984-2023%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: (01)00843997000239 Lot #: K16ANC, K16MWR, K17AEU, 17EGQ |

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

## Distribution

US: AK , AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY OUS: Argentina, Australia, Austria, Belgium, Bermuda, Brazil, Canada, Chile, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Finland, France, Germany, Gibraltar, Guernsey, Hong Kong, Hungary, Iceland, India, Israel, Italy, Japan, Jersey, Jordan, Kenya, Lebanon, Malaysia, Malta, Mexico, Morocco, Netherlands, New Zealand, Norway, Oman, Palestinian Territory, Poland, Portugal, Puerto Rico, Qatar, Russian Federation, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Vietnam.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jun 28, 2023
- **Recall initiation date**: Apr 21, 2023
- **Center classification date**: Jun 21, 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-1984-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Masimo Corporation records](https://isitonrecall.com/brand/masimo-corporation/)
