LMA — Class II medical device recall Z-3212-2017
Terminated recall by Teleflex Medical, reported 2017-10-04, distributed nationwide. Teleflex Medical is recalling the affected product because there may be missing or incomplete information on t
| Recall number | Z-3212-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2017-07-05 |
| Classified | 2017-09-26 |
| Reported by FDA | 2017-10-04 |
| Terminated | 2018-11-20 |
| Distributed | Nationwide (US) |
| Quantity | 135,456 units |
| Reason classes | labeling |
| Lot numbers | MAD600 |
Product
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
Reason for recall
Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3212-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.