Reported Jul 1, 2026 · Ongoing · Updated Sep 16, 2026
Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
IPG Medical Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: IPG Medical Corporation · 225 Cedar Hill St · Marlborough, MA · 01752-5900
Is this the product you have?
- Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
- Lot codes and dates
201 of 201 codes
Model No. MD2300F-001507UDI-DI 00810071230226Serial No. MDUF250342MDUF250400MDUF250429MDUF250060MDUF250061MDUF250067MDUF250068MDUF250069MDUF250071MDUF250076MDUF250083MDUF250086MDUF250091MDUF250092MDUF250104MDUF250131MDUF250133MDUF250134MDUF250159MDUF250160MDUF250199MDUF250200MDUF250202MDUF250203MDUF250204MDUF250205MDUF250240MDUF250241MDUF250242MDUF250278MDUF250297MDUF250299MDUF250312MDUF250314MDUF250325MDUF250340MDUF250341MDUF250351MDUF250352MDUF250355MDUF250367MDUF250368MDUF250370MDUF250380MDUF250384MDUF250385MDUF250395MDUF250399MDUF250409MDUF250410MDUF250427MDUF250430MDUF250431MDUF250433MDUF260009MDUF260010MDUF260011MDUF260017
- Amount recalled
- 198 units
Where it was sold
- Nationwide
- MA
Why it was recalled
Software anomaly that causes a false display of error code 5018.
This product could cause temporary or reversible health problems — stop using it.
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