Reported Nov 27, 2019 · Ongoing

WECK Hem-O-Lok AutoEndo5, 5mm Automatic Endoscopie Hem-o-lok Applier, REF 543965 Automatic Endoscopic Surgical Ligating…

Teleflex Medical

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 Medical · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437

Is this the product you have?

  • WECK Hem-O-Lok AutoEndo5, 5mm Automatic Endoscopie Hem-o-lok Applier, REF 543965 Automatic Endoscopic Surgical Ligating Clip Appliers are delivery devices for Hem-o-lok ML non-absorbable polymer ligating clips
Lot codes and dates
  • Codes

    188 of 188 codes

    • 73J1600836
    • 73C1700518
    • 73D1800018
    • 73H1800233
    • 73A1900664
    • 73J1600837
    • 73C1700842
    • 73D1800019
    • 73H1800234
    • 73B1900436
    • 73K1600114
    • 73D1700008
    • 73D1800020
    • 73H1800235
    • 73B1900437
    • 73K1600115
    • 73D1700009
    • 73D1800558
    • 73H1800236
    • 73B1900438
    • 73K1600290
    • 73D1700010
    • 73D1800559
    • 73H1800240
    • 73K1600515
    • 73D1700068
    • 73D1800560
    • 73H1800496
    • 73K1600814
    • 73D1700069
    • 73D1800561
    • 73H1800497
    • 73L1600097
    • 73D1700313
    • 73D1800562
    • 73H1800498
    • 73L1600098
    • 73D1700314
    • 73D1800563
    • 73H1800499
    • 73L1600099
    • 73D1700315
    • 73D1800564
    • 73H1800500
    • 73L1600100
    • 73D1700496
    • 73D1800565
    • 73H1800501
    • 73L1600101
    • 73D1700497
    • 73E1800526
    • 73H1800502
    • 73L1600274
    • 73D1700574
    • 73E1800527
    • 73H1800639
    • 73L1600275
    • 73D1700575
    • 73E1800528
    • 73H1800640
Amount recalled
4099 devices

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Certain clip appliers have an increase in misloading and/or jamming related complaints that may be due to a discrepancy in the specification a component. Misloading and/or jamming may lead to clips falling out of the applier, clip breakage, or the jaws becoming locked in a partially closed position (jammed).

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.