Teleflex Medical Europe Ltd: Medical Device Recall in 2018 - (Recall #: Z-1628-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 19, 2018

Date Posted: May 9, 2018

Recall Number: Z-1628-2018

Event ID: 79643

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: 25 units

Code Information:

Lot Number 161212

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated