FDA Recall Terminated

Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube with TaperGuard Cuff. Intended for use in providing tracheal access for airway managements.

Recall: Z-1951-2015 · Initiated May 8, 2015

Recall

Recall Number
Z-1951-2015
Event Number
71197
Firm
Covidien LP (formerly Nellcor Puritan Bennett Inc.)
FEI Number
2936999
Product Code
JOH
Status
Terminated
Root Cause
Device Design
Initiated
May 8, 2015
Posted
July 9, 2015
Terminated
April 12, 2017
Address
6135 Gunbarrel Ave, Boulder, CO, 80301-3214

Description

Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube with TaperGuard Cuff. Intended for use in providing tracheal access for airway managements.

Reason

Reports where patients who recently switched from the current Shiley Neonatal and Pediatric products to the affected products experienced discomfort and in some cases, breathing difficulties, corresponding to a negative effect on oxygen levels.

Action

Consignees were notified 5/8/15 via letter. Consignees were asked to return products.

Distribution

Worldwide Distribution. US nationwide, Canada, Australia, Belgium, Chile, Germany, Israel, Italy, Japan, Saudi Arabia, Singapore, South Africa, Turkey, and Uruguay.

Quantity

69,461 units total