Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Teleflex HORIZON Microclip Titanium Ligating Clips w/tape Recalled by TELEFLEX LLC Due to Teleflex LLC is initiating this voluntary field corrective...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact TELEFLEX LLC directly.
Affected Products
Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or tissue ligation
Quantity: 146,606 units
Why Was This Recalled?
Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts the application of the clip to the applier. With this step feature missing on the cartridge, the clip is mounted in a more variable position, allowing the clips to load farther back in the clip applier jaw grooves. This may potentially result in inappropriate or inadequate clip application to vascular structures.
Where Was This Sold?
worldwide
About TELEFLEX LLC
TELEFLEX LLC has 139 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report