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Medical Device

PNE Lead Implant Kit REF: 1701

Recall date: 2026-10-28 · Source: FDA_DEVICE
Brand / Firm
Axonics, Inc.
Product
PNE Lead Implant Kit REF: 1701
Reason for recall
Retroactively Reported: 10mL luer lock syringes included in kit may leak , break or experience other issues that may pose a risk to users.
Units affected
18,294 kits
Description
PNE Lead Implant Kit REF: 1701
View official recall notice →