FDA Device Recalls

Recalls /

#27968

Product

Fibered Platinum Coil, 0.035 Type, 9 mm x 60 mm Catalog no. 372906

510(k) numbers
K955293
Affected lot / code info
Lot Number: 5472234

Why it was recalled

Product 's Outer box label may not match pouch label: a 4mm x 30 mm coil may be labeled as a 9 mm x 60 mm or vice versa

Root cause (FDA determination)

Other

Action the firm took

Boston Scientific notified sales representatives on 6/23/03 in foreign distribution area to remove product from inventory and contact hospital to retrieve and return.

Recalling firm

Firm
Boston Scientific Corporation
Address
1 Boston Scientific Place, Natick, Massachusetts 01760

Distribution

Distribution pattern
Japan, Italy, France, Turkey, Israel, Finland

Timeline

Recall initiated
2003-06-23
Posted by FDA
2003-07-19
Terminated
2018-10-03
Status

Source: openFDA Device Recall endpoint. Recall record ID #27968. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

— recall: Fibered Platinum Coil, 0.035 Type, 9 mm x 60 mm Catalog no. 372906 · FDA Device Recalls