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