LYMOL Medical Elite X Class Rigid Bronchoscope System — Class II medical device recall Z-2562-2021
Terminated recall by Lymol Medical Corporation, reported 2021-10-06, distributed nationwide. Reprocessing instructions were revised November 15, 2020, to reflect new processes and equipment used at consi
| Recall number | Z-2562-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lymol Medical Corporation, Woburn, MA, United States |
| Recall initiated | 2021-07-29 |
| Classified | 2021-09-24 |
| Reported by FDA | 2021-10-06 |
| Terminated | 2022-10-04 |
| Distributed | Nationwide (US) |
| Quantity | 309 |
| Model numbers | BA2700, BB2401, BB2402, BB2701, BB2702, BD2410, BDL2420, BI2001, BI2101, BI2103, BI2200, BI2999, BP2000, BP2101, BP2103, BP2200, BR2000, BR2101, BR2103, BR2200, BT2000, BT2101, BT2103, BT2105, BT2106 and 4 more |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2562-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.