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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K021808
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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WECK Hem-O-Lok AutoEndo5, 5mm Automatic Endoscopie Hem-o-lok Applier, REF 543965 Automatic End... 2 11/19/2019 Teleflex Medical
Weck Hemoclip Plus® Ligating Clips, Rx Only, Sterile, Teleflex Medical, RTP, NC 27709 USA. The use o... 2 09/16/2008 Telefelx Medical
Weck Hemoclip Traditional Ligating Clips, Rx Only, Sterile, Teleflex Medical, RTP, NC 27709 USA. Th... 2 09/16/2008 Telefelx Medical
Weck , Horizon Titanium Clips, Rx Only, Sterile, Teleflex Medical, RTP, NC 27709, USA. The use of t... 2 09/16/2008 Telefelx Medical
WECK Hem-o-lok®® Non-absorbable Polymer Ligation Clips, Rx Only, Sterile, Teleflex Medical, RTC, NC ... 2 09/16/2008 Telefelx Medical
WECK HemoClip Auto, Rx Only, Sterile, Teleflex Medical, RTC, NC 27709. The use of the reusable Tele... 2 09/16/2008 Telefelx Medical
Weck Hem-o-lok Endo 5 Automatic Clip Applier with Medium Polymer Ligating Clips; Rx, sterile, single... 2 06/09/2006 Teleflex Medical
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