Atlas FDA

CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with a ventila

FDA device recall Z-2689-2014 · posted 2014-09-23 · Terminated

Recall details

Recalling firm
Carefusion 2200 Inc
Reason for recall
The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due to a regulatory compliance risk involving a material change. The changes to the gas pathway may potentially impact the safety of the device and quality of the gas condensates to the patient.
Action taken
CareFusion sent an URGENT: PRODUCT RECALL letters dated July 31, 2014 to all affected customers. The letters instructed customers to: 1) perform a 100% physical inventory to verify if any of the affected product codes are in stock; 2) complete and return the attached Recall Response Form within 15 days; 3) notify any customers/parties that the recalled products were distributed to of the recall; 4) distributors should have all their customers return the products and a completed Recall Response Form to the distributor for credit; and, 5) customers should destroy the recalled products according to their disposal procedure. If a customers procedure(s) does not allow for the destruction of the recalled products, the customers was advised to contact CareFusion AirLife Customer Support at 800-323-9088 (Monday - Friday, 8:00 AM - 5:00 PM CST) for product return options. Customers will receive credit for all destroyed products. Direct accounts with questions about this recall should contact CareFusion AirLife Customer Support at 800-323-9088 (Monday - Friday, 8:00 AM - 5:00 PM CST) for additional information.
Root cause
No Marketing Application
Status
Terminated
Product code
BZE
Quantity affected
Approximately 318,280 devices
Distribution
Worldwide Distribution - US Nationwide in the states of AZ, CA, FL, IL, KY, LA, MI, MO, NE, NY, OH, OK, PA, RI, TN, TX, UT including Puerto Rico and the countries of Canada, China, Kuwait, Mexico, Sau
Date initiated
2014-07-31
Date posted
2014-09-23
Date terminated
2016-02-08
Location
Vernon Hills, IL

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Related 510(k) clearances

RecordFirmDate
ISOTHERMAL HEATED VENTILATOR & ANESTHESIA CIRCUIT (K915226)Baxter Healthcare Corp1993-01-12