OtoLase Starter Kit; UPN: AC-2003748. Indicated for a variety of surgical uses including ablation, coagulation, incision, excision, and vaporization of soft tissue.
FDA Recall Z-2344-2025 · Posted 2025-08-21
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Recalling FirmLUMENIS, LTD.
Recall StatusOpen, Classified
Product CodeGEX
Date Initiated2025-07-22
Product Quantity13 units
Reason for Recall
The potential for unsterilized product within finished product labeled as sterile.
Firm Action
On July 22, 2025, URGENT MEDICAL DEVICE REMOVAL - IMMEDIATE ACTION REQUIRED letters were sent to customers.
Instructions:
" Immediately discontinue use and segregate the affected products to prevent accidental use and
follow provided removal instructions on the attachment.
" Post this information in a visible location near where the affected products are stored to ensure this
information is readily accessible to all handlers and users of the device. Share this notice with any
healthcare professional within your organization and with any organization where the affected
products may have been transferred.
" If you are a distributor, this notification must be forwarded to your customers to ensure notification
of this product removal is carried out to the end-user level.
" If you are a facility that has sent products to another hospital or a facility within your network, ensure
this notification is forwarded to them.
Any adverse events or quality concerns associated with use of these devices should be reported to Boston
Scientific via email at [email protected] or FDA s MedWatch Adverse Event Reporting
program [www.fda.gov/MedWatch/report.htm or 1.800.FDA.1088 (332.1088)].
We appreciate your understanding as we take action to address this issue. At Boston Scientific, patient
safety and customer satisfaction are our priority. We are committed to continuing to offer products that meet
the quality standards that you expect from Boston Scientific.
Contact your local Boston Scientific representative with any questions.
Root Cause
Nonconforming Material/Component
Distribution Pattern
Domestic: PA, WI; International: Germany, India;
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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