# FDA recall Z-0010-2023

> **Hobbs Medical, Inc.** · Class II · device recall initiated 2022-07-29.

## Product

Hobbs Medical Spray Catheter: The Mistifier: 2.6mm	260cm  Disposable For endoscopy procedures  Ref: 2190

## Reason for recall

Device label display an incorrect expiration date, extends the shelf life of the product. Affected product  distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and 2025-09-01 (Devices have a lot number ending in R, or are kits containing at least 1 device with a lot number ending in R.)

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Austria, Belgium, Finland, Norway.

## Key facts

- **Recall number:** Z-0010-2023
- **Recalling firm:** Hobbs Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-29
- **Report date:** 2022-10-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Stafford Springs, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0010-2023

## Citation

> AI Analytics. FDA recall Z-0010-2023. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-0010-2023. Source: US FDA. Licensed CC0.

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