The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
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 Medtronic Navigation, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-3057-2017 — Medtronic Navigation, Inc. Medtronic Navigation, Inc. recalls Medtronic Set Supplemental INS AxiEM Hello, I own a Medtronic Navigation, Inc. recalls Medtronic Set Supplemental INS AxiEM ENT, Ref. 9734378, reusable, RX. This kit contains 9734308, Small Straight that is covered by recall Z-3057-2017 from Medtronic Navigation, Inc.. 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.
