Ref. No. 533735 and 534735 Hemoclip Plus, 25 Small Titanium Clips, Cartridge; Ref. No. 533870 Hemoclip Plus, 10 Large Titanium Clips/Cartridge and Ref. No. 533700 Hemoclip Plus, 25 Medium Titanium Clips/Cartridge Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ref. No. 533735 and 534735 Hemoclip Plus, 25 Small Titanium Clips, Cartridge; Ref. No. 533870 Hemoclip Plus, 10 Large Titanium Clips/Cartridge and Ref. No. 533700 Hemoclip Plus, 25 Medium Titanium Clips/Cartridge
Lot Codes / Batch Numbers
All lots manufactured between 2001-8 through 2002-12 for all three products and lots 738967, 763871 and 714124 for 25 Small Titanium Clips, lots 703251, 722666 and 825952 for 10 Large Titanium Clips and lots 738966, 754641 and 824238 for 25 Medium Titanium Clips
Products Sold
All lots manufactured between 2001-8 through 2002-12 for all three products and lots 738967, 763871 and 714124 for 25 Small Titanium Clips; lots 703251, 722666 and 825952 for 10 Large Titanium Clips and lots 738966, 754641 and 824238 for 25 Medium Titanium Clips
A medical device manufacturer is recalling Ref. No. 533735 and 534735 Hemoclip Plus, 25 Small Titanium Clips, Cartridge; Ref. No. 533870 Hemocl due to Hole in the sterile unit blister pack that could compromise sterility.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Hole in the sterile unit blister pack that could compromise sterility.
Recommended Action
Per FDA guidance
The consignees were notified of the recall via letter beginning October 24, 2003 asking for return of 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 noticePage updated: Jan 10, 2026