Arrow International Inc 10 FR Super Arrow-Flex Percutaneous Sheath Introducer Set Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
10 FR Super Arrow-Flex Percutaneous Sheath Introducer Set
Brand
Arrow International Inc
Lot Codes / Batch Numbers
Catalog/Model number CL-07011, Lot number CF03075226
Products Sold
Catalog/Model number CL-07011, Lot number CF03075226
Arrow International Inc is recalling 10 FR Super Arrow-Flex Percutaneous Sheath Introducer Set due to package lid identifies the contents incorrectly. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
package lid identifies the contents incorrectly
Recommended Action
Per FDA guidance
The recalling firm notified the consignees via telephone on 10/22/03 regarding the problem and the need to return the product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AR, CA, IN, NH, VT, VA
Page updated: Jan 10, 2026