10 FR Super Arrow-Flex Percutaneous Sheath Introducer Set
This recall has been terminated (originally issued November 1, 2003).
- Company
- Arrow International Inc
- Recall Initiated
- October 22, 2003
- Posted
- November 1, 2003
- Terminated
- April 5, 2004
- Recall Number
- Z-0088-04
- Quantity
- 80 units
- Firm Location
- Reading, PA
- Official Source
- View on FDA website ↗
Reason for Recall
package lid identifies the contents incorrectly
Distribution
The products were shipped to medical facilities in AR, CA, NH, VA and VT. The product was also shipped to a distributor in Srialanka
Lot / Code Info
Catalog/Model number CL-07011, Lot number CF03075226
Root Cause
Other
Action Taken
The recalling firm notified the consignees via telephone on 10/22/03 regarding the problem and the need to return the product.
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