FDA Recall Open, Classified

Extension Set, EXT SET W/CARESITE, 6IN., Product Code 470169, 50 units per carton. A6 Access Device is a valve intended for the aspiration, injection or gravity/pump flow of IV fluids and blood upon insertion of a male luer connector.

Recall: Z-0091-2023 · Initiated September 15, 2022

Recall

Recall Number
Z-0091-2023
Event Number
90850
Firm
B. Braun Medical, Inc.
FEI Number
2523676
Product Code
FPA
Status
Open, Classified
Root Cause
Process design
Initiated
September 15, 2022
Posted
October 14, 2022
Address
901 Marcon Blvd, Allentown, PA, 18109-9512

Description

Extension Set, EXT SET W/CARESITE, 6IN., Product Code 470169, 50 units per carton. A6 Access Device is a valve intended for the aspiration, injection or gravity/pump flow of IV fluids and blood upon insertion of a male luer connector.

Reason

The extension set has a high probability of failure which could lead to possible leakage or detachment at the device's bonded joint during use. The issue may result in delay of therapy, increased risk of bloodstream infections (BSI), and may expose both patients and healthcare workers to hazardous medications. Depending on the nature of the leak and type of infusion, there is also the potential for life-threatening situations to occur including air embolization or hypovolemia.

Action

On September 15, 2022, the firm notified affected customers via Urgent Medical Device Recall letters. Customers were instructed to cease use and quarantine the product subject to recall. Once customers have returned the completed acknowledgement form to B. Braun Medical Inc., a Customer Support representative will contact the customer with instructions on returning impacted cases. The firm will provide credit and/or replacement of the product based on the customer's needs. For questions, please contact BBMI's Postmarket Surveillance Department at 1-833-425-1464.

Distribution

Distribution US nationwide, Canada and Saudi Arabia.

Quantity

354,200 US; 1,800 OUS