Terumo L Series 1863 type arterial perfusion cannulae, straight open tip, 1/4'' connector, arterial cannula, 12 FR, 17.5
FDA device recall Z-0544-2007 · posted 2007-02-27 · Terminated
Recall details
- Recalling firm
- Terumo Cardiovascular Systems Corp
- Reason for recall
- The cannula connector is an incorrect size: It is actually 1/4" by 3/8" instead of the correct 1/4" by 1/4".
- Action taken
- Consignee was notified via telephone on 12/7/06 and returned the product.
- Root cause
- Other
- Status
- Terminated
- Product code
- DWF
- Quantity affected
- 10
- Distribution
- Pennsylvania.
- Date initiated
- 2006-12-07
- Date posted
- 2007-02-27
- Date terminated
- 2007-12-05
- Location
- Ann Arbor, MI
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| BARD(R) WILLIAM HARVEY(R) ARTERIAL STRAIGH CANNULA (K930620) | C.R. Bard, Inc. | 1993-05-07 |