# FDA recall Z-2273-2026

> **Covidien LLC** · Class II · device recall initiated 2026-04-23.

## Product

Covidien Mon-a-Therm general purpose temperature probe   size: 9 Fr  REF: 90050

## Reason for recall

Temperature probe devices lack FDA clearance.

## Distribution

US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV.

## Key facts

- **Recall number:** Z-2273-2026
- **Recalling firm:** Covidien LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-23
- **Report date:** 2026-06-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Boulder, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2273-2026

## Citation

> MORVS. FDA recall Z-2273-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2273-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*