Olympus America Inc. Olympus Single Use Mechanical Lithotriptor, Model Number BML-V232QR-26, Olympus America, Inc. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Olympus Single Use Mechanical Lithotriptor, Model Number BML-V232QR-26, Olympus America, Inc.
Brand
Olympus America Inc.
Lot Codes / Batch Numbers
Model number BML-V232QR-26: Lot numbers 75K, 76K, and 77K.
Products Sold
Model number BML-V232QR-26: Lot numbers 75K, 76K, and 77K.
Olympus America Inc. is recalling Olympus Single Use Mechanical Lithotriptor, Model Number BML-V232QR-26, Olympus America, Inc. due to Slider knob does not move smoothly causing the user difficulty in advancing the coil sheath. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Slider knob does not move smoothly causing the user difficulty in advancing the coil sheath
Recommended Action
Per FDA guidance
The recalling firm issued a recall letter dated 9/20/07 to the medical facilities informing them of the problem and the need to return the product. The letter also informed the hospitals that replacement products would be sent.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026