Teleflex Medical recalls MAD700 laryngotracheal mucosal atomization device due to potential missing or incomplete package label information. Affected units may not have proper labeling for topical anesthetic use.
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
Teleflex Medical is recalling their MAD700 laryngotracheal mucosal atomization device because the package label might be missing or incomplete. This could affect safe use for topical anesthetic applications in the oropharynx and upper airway.
The device may have missing or incomplete information on the package label. This could lead to improper use if the user cannot verify the correct labeling for topical anesthetic applications. However, the hazard does not involve physical risks like injury or malfunction.
Healthcare professionals using the device for topical anesthetic applications in the oropharynx and upper airway are most likely affected. The risk is low as the hazard involves labeling information rather than physical safety issues.
Check for the product name 'Teleflex MEDICAL LMA(TM) MADgic(TM) Laryngotracheal Mucosal Atomization Device, MAD700' with lot number 161212. The device is intended for topical anesthetic use in the oropharynx and upper airway.
Verify that the package label contains complete information for topical anesthetic use in the oropharynx and upper airway.
Teleflex Medical is recalling the device because there may be missing or incomplete information on the package label.
Check the package label for complete information about topical anesthetic use in the oropharynx and upper airway. If the label is missing or incomplete, contact Teleflex Medical for guidance.
The recall is due to labeling issues, not physical risks. There is no indication of injury risk from the device itself.
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1628-2018 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-1628-2018 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.
