RecallDepth

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

Company
Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland
Recall Initiated
March 19, 2018
Terminated
August 27, 2019
Recall Number
Z-1628-2018
Quantity
25 units

Reason for Recall

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

Distribution

TX

Lot / Code Info

Lot Number 161212

Root Cause

Process control

Action Taken

The recall notice was disseminated by letter on 03/19/2018. The letter stated the following: "1. If you have affected stock, immediately discontinue use and quarantine any products with the product code and lot number listed above. 2. To return product, complete the enclosed Recall Acknowledgement Form and fax it to 1-855-419-8507, Attn: Customer Service or email to recalls@teleflex.com. This will allow us to document the amount of product you have on hand for return. A customer service representative will contact you with a Return Goods Authorization (RGA) Number and will provide instructions for the return of products to Teleflex Medical. 3. If you have no affected stock, please complete the enclosed Recall Acknowledgment Form and fax it to 1-855-419-8507, Attn: Customer Service or email to recalls@teleflex.com. This will allow us to document your receipt of this letter."

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