Reported Jun 7, 2023 · Ongoing
Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that…
Teleflex LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: TELEFLEX LLC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
- Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or tissue ligation
- Lot codes and dates
- UDI/DI 24026704696394
- Lot Numbers
73A220085773A230001873A230017673A230032673A230052073A230077873D220021673D220055973E220063473E220087473E220109973F220019373F220020073F220048273F220071173G220016873G220034573G220056073G220075473H220011573H220029473H220043373H220045373J220074773J220076373K220001473K220009573K220010173K220029973K220056673K220071373L220006473L2200066
- Amount recalled
- 146,606 units
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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