Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-3212-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 5, 2017

Date Posted: October 4, 2017

Recall Number: Z-3212-2017

Event ID: 77980

Reason for Recall:

Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.

Status: Terminated

Product Quantity: 135,456 units

Code Information:

Lot Numbers: (a) MAD600 MADgic: 161217, 161218, 161228 (b) MAD700 MADgic: 161119, 161120, 161121, 161153, 161173, 161212, 161223, 161236 (c) MAD720 MADgic: 161154

Distribution Pattern:

Nationwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated