# FDA recall Z-3212-2017

> **Teleflex Medical** · Class II · device recall initiated 2017-07-05.

## 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.

## Distribution

Nationwide distribution

## Key facts

- **Recall number:** Z-3212-2017
- **Recalling firm:** Teleflex Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-05
- **Report date:** 2017-10-04
- **Termination date:** 2018-11-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Research Triangle Park, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3212-2017

## Citation

> AI Analytics. FDA recall Z-3212-2017. Retrieved 2026-09-08 from https://api.ai-analytics.org/recall/Z-3212-2017. Source: US FDA. Licensed CC0.

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