Terumo Cardiovascular Systems Corp Terumo Sarns brand Soft-Flow Aortic Cannula with flange, angled, wire-reinforced, with Luer, 6 mm (18 Fr) OD with 3/8 inch connector, 14 inches (35 cm) long; catalog number 7080. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Terumo Sarns brand Soft-Flow Aortic Cannula with flange, angled, wire-reinforced, with Luer, 6 mm (18 Fr) OD with 3/8 inch connector, 14 inches (35 cm) long; catalog number 7080.
Brand
Terumo Cardiovascular Systems Corp
Lot Codes / Batch Numbers
All lots (0332197, 0349597, 0360492, 0369078, 0373045, 0382401, 0391806 and 0399838).
Products Sold
All lots (0332197, 0349597, 0360492, 0369078, 0373045, 0382401, 0391806 and 0399838).
Terumo Cardiovascular Systems Corp is recalling Terumo Sarns brand Soft-Flow Aortic Cannula with flange, angled, wire-reinforced, with Luer, 6 mm (1 due to The product is labeled as sterile, but the firm has determined that the suture flange may tear through the front of the package.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product is labeled as sterile, but the firm has determined that the suture flange may tear through the front of the package.
Recommended Action
Per FDA guidance
Consignees were notified via telephone, and a recall letter dated 10/19/05 sent to each consignee, beginning on 10/18/05. International affiliates were notified via email.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IN, MO
Page updated: Jan 10, 2026