FDA Recall Open, Classified

TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV, Article No. 7S3070. Singapore only. IV injection set.

Recall: Z-0132-2024 · Initiated September 26, 2023

Recall

Recall Number
Z-0132-2024
Event Number
93074
Firm
B. Braun Medical, Inc.
FEI Number
2523676
Product Code
FPA
Status
Open, Classified
Root Cause
Process control
Initiated
September 26, 2023
Posted
November 3, 2023
Address
901 Marcon Blvd, Allentown, PA, 18109-9512

Description

TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV, Article No. 7S3070. Singapore only. IV injection set.

Reason

Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.

Action

On September 26, 2023, the firm notified customers via Urgent Product Recall Notification letters. Customers were informed of the potential for leakage at the male Luer lock site. Customers were instructed to report total amount of impacted product on hand to the firm, after which B Braun Customer Support will contact the customer with instructions on how to return the product for credit or replacement depending on the customer's need. Questions about this recall may be reported to BBMI s Postmarket Surveillance Department by calling 1-833-425-1464.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada and Singapore.

Quantity

12,800 units