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.