# FDA recall Z-2562-2021

> **Lymol Medical Corporation** · Class II · device recall initiated 2021-07-29.

## Product

LYMOL Medical Elite X Class Rigid Bronchoscope System, Part No. BD2410, BB2701, BB2702, BB2401, BB2402, BA2700, BT2000, BT2101, BT2103, BT2105, BT2106, BT2210, BT2201, BT2203, BT2205, BR2200, BP2200, BI2200, BR2000, BP2000, BI2999, BR2103, BP2103, BI2103, BR2101, BP2101, BI2101, BI2001, BDL2420

## Reason for recall

Reprocessing instructions were revised November 15, 2020, to reflect new processes and equipment used at consignee user facilities. New instructions were not sent to all consignees of the devices at the time of the revision.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2562-2021
- **Recalling firm:** Lymol Medical Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-29
- **Report date:** 2021-10-06
- **Termination date:** 2022-10-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Woburn, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2562-2021

## Citation

> AI Analytics. FDA recall Z-2562-2021. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-2562-2021. Source: US FDA. Licensed CC0.

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