Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol Medical Corporation Due to Reprocessing instructions were revised November 15, 2020, to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lymol Medical Corporation directly.
Affected Products
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
Quantity: 309
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lymol Medical Corporation
Lymol Medical Corporation has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report