FDA Device recall Z-1628-2018
Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the application of topical ane…
- FDA Device
- Class II
- terminated
- Published 2018-05-09
On 2018-05-09 the FDA classified a Class II recall of Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the application of topical ane… by Teleflex Medical Europe, citing teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1628-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-19 |
| Published | 2018-05-09 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Teleflex Medical Europe |
| Distribution | TX |
Product
Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the application of topical anesthetics to the oropharynx and upper airway region
Reason
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
Identifiers
| code_info | Lot Number 161212 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1628-2018%22
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