Recalls / —

—#40681

Product

Implantable Chest Ports With PASV Valve Technology - Single Lumen - PASV Port/9.6/SL/T/A Catalog Number: M001PRTA96A0

FDA product code

KOB — Catheter, Suprapubic (And Accessories)

Device class

Class 2

Medical specialty

Gastroenterology, Urology

510(k) numbers

K991897

Affected lot / code info

Lot Numbers:  966751 967149 972362 977505 982744 984498 987583 991186 1000970 1001769 1008238 1008734 1020904 1021342 1026348 1029102

Why it was recalled

The Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.

Root cause (FDA determination)

Other

Action the firm took

Boston Scientific intiated the recall on 7/22/05 to direct accounts and to distributors on 7/ 27 /05. Distributors are requested to conduct sub recalls to the medical facility level. A revised letter dated 8/2/05 was sent to 18 US accounts for one lot (#1020895) omitted in the letter of 7/22/05.

Recalling firm

Firm

Boston Scientific Corporation

Address

1 Boston Scientific Pl, Natick, Massachusetts 01760-1536

Distribution

Distribution pattern

Nationwide VA Hopsitals Foreign: Canada, Africa, Japan, Israel, Japan, Nertherlands, Venezula

Timeline

Recall initiated

2005-07-22

Posted by FDA

2005-09-02

Terminated

2007-06-20

Status

—

Source: openFDA Device Recall endpoint. Recall record ID #40681. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.