Reported Oct 4, 2017 · Terminated

LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720…

Teleflex Medical

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Teleflex Medical · 2917 Weck Dr · Research Triangle Park, NC · 27709-0186

Is this the product you have?

  • LMA(TM) MADgic(TM) Laryngo-Tracheal
  • Mucosal Atomization Devices(a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADgic Intended for the application of topical anesthetics to the oropharynx and upper airway region
Lot codes and dates
  • Lot Numbers(a)
  • MAD600 MADgic
    • 161217
    • 161218
    • 161228 (b)
  • MAD700 MADgic
    • 161119
    • 161120
    • 161121
    • 161153
    • 161173
    • 161212
    • 161223
    • 161236 (c)
  • MAD720 MADgic161154
Amount recalled
135,456 units

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide

Why it was recalled

Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 20, 2018 · Data as of Sep 19, 5:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.