Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
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Recall Number
Z-1437-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2024-09-13
Reported
2026-03-04
Distribution
Distribution US nationwide.
Code Info
Model: WA2280A; UDI: 04042761051729; Lot#: All lots;
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.