Oscor, Inc. Oscor Adelante Luer-Lock Peel Away Introducer Set, for introduction of diagnostic or therapeutic devices into the body. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Oscor Adelante Luer-Lock Peel Away Introducer Set, for introduction of diagnostic or therapeutic devices into the body.
Brand
Oscor, Inc.
Lot Codes / Batch Numbers
Lot Numbers: C1-02452, C1-02453, C1-02452, C1-02458, C1-02462.
Products Sold
Lot Numbers: C1-02452, C1-02453, C1-02452, C1-02458, C1-02462.
Oscor, Inc. is recalling Oscor Adelante Luer-Lock Peel Away Introducer Set, for introduction of diagnostic or therapeutic dev due to Difficulty breaking the sheath hub and subsequently to peel the sheath off for Introducer Set, Adelante size 7F.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Difficulty breaking the sheath hub and subsequently to peel the sheath off for Introducer Set, Adelante size 7F.
Recommended Action
Per FDA guidance
Oscor notified the Direct Account by letter on 07/03/2008. Direct account was asked to return all unused Introducers back to Oscor. All returned products should be labeled with the Return Goods Product number.
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
IN, MN
Page updated: Jan 10, 2026