FDA Device Recalls

Recalls /

#64328

Product

Boston Scientific Radial Jaw Large Capacity Biopsy Forceps, Sterile, 240 mm. Box of 20 U PN Number: M00513321 REF: 1332-20

FDA product code
FFFCover, Biopsy Forceps
Device class
Class 1
Medical specialty
Gastroenterology, Urology
Affected lot / code info
Lot Number: 8990184

Why it was recalled

Device lacked manufacturing finishing process resulting in endoscope damage.

Root cause (FDA determination)

Process control

Action the firm took

Boston Scientific notified accounts by letter on 8/28/07 by Federal Express Priority mail. Accounts are requested to remove product from inventory and return product.

Recalling firm

Firm
Boston Scientific Corporation
Address
100 Boston Scientific Way, Marlborough, Massachusetts 01752-1234

Distribution

Distribution pattern
Worldwide, including USA, Sweden, and South Africa.

Timeline

Recall initiated
2007-08-28
Posted by FDA
2007-10-31
Terminated
2008-07-10
Status

Source: openFDA Device Recall endpoint. Recall record ID #64328. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

— recall: Boston Scientific Radial Jaw Large Capacity Biopsy Forceps, Sterile, 240 mm. Box of 20 U PN Number: · FDA Device Recalls