Teleflex Medical LMA MADgic Devices Recall: Missing Package Label Information
Teleflex Medical recalls LMA MADgic laryngo-tracheal mucosal atomization devices due to potential missing or incomplete package label information. Affected models include MAD600, MAD700, and MAD720 with specific lot numbers.
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 LMA MADgic laryngo-tracheal mucosal atomization devices (MAD600, MAD700, MAD720) because package labels may have missing or incomplete information. This could affect safe use of the devices for topical anesthetics in medical procedures. Read more at govinfonow.com/recall/73468-teleflex-medical-lma-madgic-devices-recall-missing-package-label-information.
Source Summary by GovInfoNow · govinfonow.com/recall/73468-teleflex-medical-lma-madgic-devices-recall-missing-package-label-information · Updated September 21, 2026 · FDA enforcement record: FDA #Z-3212-2017
Cite this page
“Teleflex Medical LMA MADgic Devices Recall: Missing Package Label Information.” GovInfoNow, updated September 21, 2026. https://govinfonow.com/recall/73468-teleflex-medical-lma-madgic-devices-recall-missing-package-label-information. Based on FDA recall #Z-3212-2017 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3212-2017%22&limit=1).
Why it’s dangerous
The devices may have missing or incomplete information on the package label, which could lead to incorrect usage or safety issues during medical procedures. This is a labeling issue rather than a physical defect in the device itself.
Who’s affected
Healthcare professionals who use these devices for topical anesthetics in medical procedures are most at risk. Patients using these devices under medical supervision may also be affected.
How to tell if you have this one
Check for the model numbers MAD600, MAD700, or MAD720 with specific lot numbers listed in the recall notice. The devices are intended for topical anesthetics in medical procedures.
- Brand
Teleflex Medical- Category
Medical device
What to do — step by step
Check Package Label
Look for missing or incomplete information on the package label of the device.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
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.
Questions people ask
What lot numbers are affected?
Lot numbers for MAD600: 161217, 161218, 161228; MAD700: 161119, 161120, 161121, 161153, 161173, 161212, 161223, 161236; MAD720: 161154.
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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-3212-2017 (July 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3212-2017 to see it in context.
- Plain-language summary written by qwen3:4b on September 21, 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.