Atlas FDA

Portex Tracheal Tube, Oral/Nasal, Murphy Eye, Clear, 2.5 mm Product Code: 100/127/025. Intended for oral and/or nasal in

FDA device recall Z-2068-2009 · posted 2009-09-18 · Terminated

Recall details

Recalling firm
Smiths Medical
Reason for recall
Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway
Action taken
Smiths Medical issued an "Urgent Field Safety Notice" dated August 24, 2009 via UPS Second Day Mail including a Guidance Chart. Return of the enclosed Confirmation Form was also requested by fax to 1-603-355-8157. Smiths Medical issued a revised recall letter dated September 9, 2009. Customers are requested to return unused affected product to the firm. For further information, contact Smiths Medical ASD, Inc. by phone at 1-800-348-6064, prompt 4 extension 2273.
Root cause
Process control
Status
Terminated
Product code
BTR
Quantity affected
17,267 (US) 9,690 (International)
Distribution
Worldwide Distribution -- United States, Andorra, Argentina, Armenia, Australia, Austria, Bahrain, Bangladesh, Barbados, Belgium, Bermuda, Borneo, Brazil, Brunei, Bulgaria, Canada, Chile, China, C¿¿te
Date initiated
2009-08-25
Date posted
2009-09-18
Date terminated
2012-11-16
Location
Hythe Kent, United Kingdom

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