Teleflex Medical LMA MADgic Laryngotracheal Mucosal Atomization Device Recall: Missing
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.
Lower-risk recall
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/71682-teleflex-medical-lma-madgic-laryngotracheal-mucosal-atomization-device-recall-missing.
Source Summary by GovInfoNow · govinfonow.com/recall/71682-teleflex-medical-lma-madgic-laryngotracheal-mucosal-atomization-device-recall-missing · Updated August 27, 2026 · FDA enforcement record: FDA #Z-1628-2018
Cite this page
“Teleflex Medical LMA MADgic Laryngotracheal Mucosal Atomization Device Recall: Missing.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/71682-teleflex-medical-lma-madgic-laryngotracheal-mucosal-atomization-device-recall-missing. Based on FDA recall #Z-1628-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1628-2018%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Teleflex Medical- Category
Medical device
What to do — step by step
Check Package Label
Verify that the package label contains complete information for topical anesthetic use in the oropharynx and upper airway.
Where it went and when
Where it was distributed
Distributed in Texas.
FDA distribution: “TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Texas.
Recall timeline
FDA terminated this recall 17 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-1628-2018 (March 19, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1628-2018 to see it in context.
- Plain-language summary written by qwen3:4b on August 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.