ELAN 4 burr/blade accessories were marketed without 510(k) premarket notification clearance.
ELAN 4 burr/blade accessories were marketed without 510(k) premarket notification clearance.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Aesculap Implant Systems LLC to request your refund or repair — edit it as you like.
Subject: Recall Z-0621-2018 — Aesculap Implant Systems LLC Aesculap Implant Systems LLC recalls ELAN 4 Blade: ELAN 4 1-RING PIN C Hello, I own a Aesculap Implant Systems LLC recalls ELAN 4 Blade: ELAN 4 1-RING PIN CUTTER D1.0 ELAN 4 1-RING NEURO CUTTER+ SOFT D1.5 ELAN 4 1-RING NEURO CUTTER+ SOFT D2.0 that is covered by recall Z-0621-2018 from Aesculap Implant Systems LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
