Total recalls 235 since 2012
Last 12 months 0 reported
Class I 50 21% of total
Ongoing 10 latest 1 Jun 2022
Recalls per month, last 24 months click a bar for that month Severity split
50 21%178 76%7 3%
Why teleflex medical is recalled
Ongoing teleflex medical recalls 10 active
All teleflex medical recalls, newest first 235 total Reported Class Recall Company Reason Where 1 Jun 2022 Device CLASS II Teleflex Flex tube, Product #20011, sterile recalled by Teleflex Medical Teleflex Medical Other Nationwide 1 Jun 2022 Device CLASS II Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile recalled Teleflex Medical Other Nationwide 23 Feb 2022 Device CLASS I Arrow-Trerotola Over-The-Wire PTD Kit recalled by Teleflex Medical Teleflex Medical Other Nationwide 23 Feb 2022 Device CLASS I Arrow-Trerotola Over-The-Wire PTD Kit recalled by Teleflex Medical Teleflex Medical Other Nationwide 23 Feb 2022 Device CLASS I Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device) recalled Teleflex Medical Other Nationwide 23 Feb 2022 Device CLASS I Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device) recalled Teleflex Medical Other Nationwide 23 Feb 2022 Device CLASS I Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device recalled Teleflex Medical Other Nationwide 23 Feb 2022 Device CLASS I Arrow-Trerotola Over-The-Wire PTD Kit recalled by Teleflex Medical Teleflex Medical Other Nationwide 23 Feb 2022 Device CLASS I Arrow-Trerotola Over-The-Wire PTD Kit recalled by Teleflex Medical Teleflex Medical Other Nationwide 31 Mar 2021 Device CLASS II Pleur-evac Thoracic Catheters (Catheter, Irrigation) recalled Teleflex Medical Sterility Nationwide 31 Mar 2021 Device CLASS II Rusch¿ Polaris" Laryngoscope recalled by Teleflex Medical Teleflex Medical Device Malfunction Nationwide 9 Sep 2020 Device CLASS II Pleur-evac Thoracic Catheters recalled by Teleflex Medical Teleflex Medical Sterility 23 states 12 Aug 2020 Device CLASS II Pleur-Evac Adult-Ped Wet, LF Intl Eng, product recalled Teleflex Medical Sterility Nationwide 12 Aug 2020 Device CLASS II Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product recalled Teleflex Medical Sterility Nationwide 5 Aug 2020 Device CLASS II Rusch Greenlite Product recalled by Teleflex Medical Teleflex Medical Device Malfunction Nationwide 5 Aug 2020 Device CLASS II Rusch Greenlite Product recalled by Teleflex Medical Teleflex Medical Device Malfunction Nationwide 5 Aug 2020 Device CLASS II Rusch Greenlite Product recalled by Teleflex Medical Teleflex Medical Device Malfunction Nationwide 5 Aug 2020 Device CLASS II Rusch Greenlite Product recalled by Teleflex Medical Teleflex Medical Device Malfunction Nationwide 5 Aug 2020 Device CLASS II Rusch Greenlite Product recalled by Teleflex Medical Teleflex Medical Device Malfunction Nationwide 5 Aug 2020 Device CLASS II Rusch Greenlite Product recalled by Teleflex Medical Teleflex Medical Device Malfunction Nationwide 5 Aug 2020 Device CLASS II Rusch Greenlite Product recalled by Teleflex Medical Teleflex Medical Device Malfunction Nationwide 15 Jul 2020 Device CLASS II Rusch Lasertube (Rubber), Res 102004, Sizes: a) I.D recalled Teleflex Medical Foreign Material Nationwide 3 Jun 2020 Device CLASS II Sprotte Needle recalled by Teleflex Medical Teleflex Medical Sterility Nationwide 3 Jun 2020 Device CLASS II Sprotte Needle recalled by Teleflex Medical Teleflex Medical Sterility Nationwide 26 Feb 2020 Device CLASS II Disposable Aortic Punch, in the following sizes: a) recalled Teleflex Medical Sterility NC 26 Feb 2020 Device CLASS II Pilling Aortic Punch Standard Tip recalled by Teleflex Medical Teleflex Medical Sterility NC 19 Feb 2020 Device CLASS I Hudson Rci Comfort Flo Corrugated Humidification System recalled Teleflex Medical Temperature Abuse Nationwide 19 Feb 2020 Device CLASS I Hudson Rci Comfort Flo Humidification System With Remote recalled Teleflex Medical Temperature Abuse Nationwide 19 Feb 2020 Device CLASS I Hudson Rci Comfort Flo Corrugated Humidification System recalled Teleflex Medical Other Nationwide 19 Feb 2020 Device CLASS II Rusch Greenlite Single-Use Metal Laryngoscope Blade recalled Teleflex Medical Device Malfunction Nationwide
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About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.