FDA Recall Terminated

Shiley PED3.0 Cuffless Pediatric Tracheostomy Tube, REF 3.0 PED, Sterile. Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Assembled in Mexico. The product is provided as one each shipped in an inner carton to end customers. The intended use of the device is to bypass upper airway obstructions, provide long term ventilation, and support and/or manage tracheal/bronchial secretions.

Recall: Z-0997-2009 · Initiated January 14, 2009

Recall

Recall Number
Z-0997-2009
Event Number
51160
Firm
Covidien Limited
FEI Number
2936999
Product Code
JOH
Status
Terminated
Root Cause
Finished device change control
Initiated
January 14, 2009
Posted
March 4, 2009
Terminated
May 21, 2012
Address
6135 Gunbarrel Ave, Boulder, CO, 80301-3214

Description

Shiley PED3.0 Cuffless Pediatric Tracheostomy Tube, REF 3.0 PED, Sterile. Tyco Healthcare Group LP, Nellcor Puritan Bennett Division, Pleasanton, CA. Assembled in Mexico. The product is provided as one each shipped in an inner carton to end customers. The intended use of the device is to bypass upper airway obstructions, provide long term ventilation, and support and/or manage tracheal/bronchial secretions.

Reason

Difficulty inserting an obturator and/or suction catheter into the tracheostomy tube.

Action

Consignees were sent an "Urgent Device Alert" letter dated 01/14/2009, by mail via Federal Express overnight delivery and instructed to evaluate any of the affected lot numbers of tracheostomy tubes prior to placement into a patient's stoma. If either the obturator or the desired sterile suction catheter does not fit properly into the tube, the tube must not be inserted into the patient. Further instructions are available at Nellcor Technical Services by calling 1-800-635-5267, option 3, then option 1. New product was expected by mid February, 2009, to address the issue.

Distribution

Nationwide Distribution, including Puerto Rico.

Quantity

8,931 units