Reported Apr 19, 2023 · Ongoing
NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue. Catalog…
Angiodynamics, Inc.
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: Angiodynamics, Inc. · 603 Queensbury Ave · Queensbury, NY · 12804-7619
Is this the product you have?
- NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue
- Catalog Number20400111
- UPNH787204001110
- Lot codes and dates
- UDI-DI15051684029643
- Lot Number5762110
- Amount recalled
- 10 boxes( 5 probes/box)
Where it was sold
Why it was recalled
Not programmed in accordance with specification. The programming affects the RFID function and does not allow the NanoKnife probes to be recognized by the NanoKnife generator resulting in a delay in procedure
This product could cause temporary or reversible health problems — stop using it.
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