Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
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 Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-3212-2017 — Teleflex Medical Teleflex Medical recalls LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization D Hello, I own a Teleflex Medical recalls LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 that is covered by recall Z-3212-2017 from Teleflex Medical. 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.
