Recall Z-0528-2025

Smiths Medical ASD, Inc. · initiated October 28, 2024

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

smiths medical PORTEX Tracheal Tube Exchange Guide, 15Ch x 70cm, REF 14-504-68 and REF 14-504-68JP

Codes / lots: REF 14-504-68, UDI/DI 35021239002586, Lot Numbers: 0003393, 0003394, 0003357, 0003358, 0003267, 0003368, 0003634, 0003254, 0003369, 0003165, 0003184, 0003196, 0003204, 0003206, 0003226, 0003256, 0003300, 0003307, 0003308, 0003314, 0003322, 0003359, 0003360, 0003361, 0003362, 0003363, 0003364, 0003377, 0003380, 0003635, 0003643; REF 14-504-68JP, UDI/DI 35021239002586, Lot Numbers: 0003369, 0003377, 0003393, 0003394, 0003634, 0003635, 0003643

Reason for recall

Smiths Medical has identified a potential for ingress of fluid into the device during reprocessing. The ingress takes place at the rear of the device between the end cap and the tube. This could lead to staining of the device or allowing the fluid to remain in the device. In addition, the Hypochlorite Solution (200ppm) and the 4% Acetic Acid disinfectants recommended in the IFU may be inadequate according to the disinfection standards for this type of device.

FDA-determined cause: Under Investigation by firm

Action taken

Smiths Medical issued an URGENT MEDICAL DEVICE REMOVAL notice to its consignees on 10/28/2024, mailed using a traceable means. The notice explained the issue, potential risk, and requested the consignee locate and destroy all affected products, and distribute the notice to all affected parties. Distributors were directed to notify their customers. For questions: About the communication: smithsmedical7602@sedgwick.com, 1-800-913-3897; To report adverse events: globalcomplaints@icumed.com, 1-866-216-8806

Details

Recall number
Z-0528-2025
Initiated
October 28, 2024
Posted by FDA
November 25, 2024
Product code
BSR – Stylet, Tracheal Tube
Quantity
10,223 units
Distribution
Worldwide distribution.
Recalling firm
Smiths Medical ASD, Inc., Minneapolis, MN

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0527-2025 Class IIsmiths medical portex Venn Reusable Tracheal Tube Introducer, 15Ch x 60cm, REF 14-504-17…Smiths Medical has identified a potential for ingress of fluid into the device during reprocessing. The… 10/28/2024Open, Classified
Z-0529-2025 Class IIsmiths medical PORTEX Tracheal Tube Exchange Guide, 10Ch x 70cm, REF 14-504-76Smiths Medical has identified a potential for ingress of fluid into the device during reprocessing. The… 10/28/2024Open, Classified