Oscor Inc. Introducer Set. Labeled as ''Luer-Lock Peel-Away Introducer Set *** Model: LLP-7 *** Size: 7F (2.33mm)'' Catalog # 06607 (Oscor) and 666089-201 (Guidant) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Introducer Set. Labeled as ''Luer-Lock Peel-Away Introducer Set *** Model: LLP-7 *** Size: 7F (2.33mm)'' Catalog # 06607 (Oscor) and 666089-201 (Guidant)
Brand
Oscor Inc.
Lot Codes / Batch Numbers
BBraun Lot # 60710907 and 60710908 Oscor Lot # OL09342-1 and OL9645-01
Products Sold
BBraun Lot # 60710907 and 60710908 Oscor Lot # OL09342-1 and OL9645-01
Oscor Inc. is recalling Introducer Set. Labeled as ''Luer-Lock Peel-Away Introducer Set *** Model: LLP-7 *** Size: 7F (2.33m due to Sheath size is larger than dilator size causing insertion difficulties.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sheath size is larger than dilator size causing insertion difficulties.
Recommended Action
Per FDA guidance
The firm will issue a recall letter to its consignees informing them of the recall. The letter will ask the consignees to return the devices from affected lot numbers for replacement. The returned products will be individually inspected.
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 noticePage updated: Jan 10, 2026