ClearanceBrief
Recall Z-0793-2020 ยท FPA Set, Administration, Intravascular

Baxter Healthcare Corporation

Clearlink System Continu-Flo Administration Sets, Product Codes: 2C8519, 2C8537, and 2C8541 - Product Usage:For the administration of fluids from a container into the patients vascular system through a vascular access device.

DateDec 12, 2019
StatusOpen, Classified
ReasonContinu-Flo sets with male Luer bodies at the lower end of, and within, the ISO specification for outer diameter require a higher than expected connection force to fully inset and securely tighten the Luer to the ONE-LINK connector.
Root causeDevice Design
ActionThe firm disseminated an urgent medical device correction notice on 12/12/2019. The notice explained the issue and provided the following actions be taken: 1. Baxter will be tightening its internal specifications for the D mold to produce Luers that target the mid to upper range of the ISO specification (target date December 2019). Additional actions, as needed, will be determined through investigation. 2. If you purchased this product directly from Baxter, complete the enclosed Baxter customer reply form and return it to Baxter by faxing it to 224-270-5457 or scanning and e-mailing it to f
Quantity271,014,984 units
DistributionWorldwide distribution - US Nationwide distribution and countries of Bermuda, Bahamas, Trinidad and Tobago, Grand Cayman, St. Thomas, Guyana and Barbados, Mexico, Canada, and New Zealand.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K961225CONTINUFLO SOLUTION SET/SECONDARY MEDICATION SET
Baxter Healthcare Corp, Jun 21, 1996