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TELEFLEX MEDICAL Recalls
236 recalls on record · July 25, 2012 to June 1, 2022 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 1, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls (1) Teleflex Flex tube, Product #20011, sterile; (2) Teleflex Smooth-Flo Flex with Double Swivel, Product #22511, steri
Hazard: Reports received of torn corrugated breathing tubes.
June 1, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-steril
Hazard: Reports received of torn corrugated breathing tubes.
February 23, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The Arrow-Trerotola Per
Hazard: The firm received reports indicating PTD tip separation during use.
February 23, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls 5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Thrombolytic Device, REF PT-65509-HFC containing components: PT-030
Hazard: The firm received reports indicating PTD tip separation during use.
February 23, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), PT-45509 containing components: PT-45509-S6, PT-45509-T
Hazard: The firm received reports indicating PTD tip separation during use.
February 23, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-WC containing components: PT-657
Hazard: The firm received reports indicating PTD tip separation during use.
February 23, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component: PT-65709-C
Hazard: The firm received reports indicating PTD tip separation during use.
February 23, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65
Hazard: The firm received reports indicating PTD tip separation during use.
February 23, 2022Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-127
Hazard: The firm received reports indicating PTD tip separation during use.
March 31, 2021Medical DevicesFDA
TELEFLEX MEDICAL INC recalls PLEUR-EVAC Thoracic Catheters (CATHETER, IRRIGATION). The thoracic catheter is a sterile, non pyrogenic, single use devi
Hazard: Teleflex is recalling this product due to a lack of assurance of sterility.
March 31, 2021Medical DevicesFDA
TELEFLEX MEDICAL INC recalls RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is u
Hazard: Teleflex is voluntarily recalling the products referenced above due to customers reporting that the laryngoscope handles develop cracks and/or break at the hinge.
September 9, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical pro
Hazard: Potential sterility issue
August 12, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST DRAINAGE: To evacuate air and/
Hazard: Potential for sterile packaging to be compromised¿
August 12, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Pleur-Evac Adult-Ped Wet, LF Intl Eng, product code: A-8000I - Product Usage: CHEST DRAINAGE: To evacuate air and/or flu
Hazard: Potential for sterile packaging to be compromised¿
August 5, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device inten
Hazard: Breaking at the point of a welded joint
August 5, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) - Product Usage: The laryngoscope is a device int
Hazard: Breaking at the point of a welded joint
August 5, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) - Product Usage: The laryngoscope is a device int
Hazard: Breaking at the point of a welded joint
August 5, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) - Product Usage: The laryngoscope is a device int
Hazard: Breaking at the point of a welded joint
August 5, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) - Product Usage: The laryngoscope is a device int
Hazard: Breaking at the point of a welded joint
August 5, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) - Product Usage: The laryngoscope is a device in
Hazard: Breaking at the point of a welded joint
August 5, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device int
Hazard: Breaking at the point of a welded joint
July 15, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 1
Hazard: Teleflex is initiating a voluntary recall for the above-mentioned products due to reports indicating that the laser guard foil partially separated and/or slightly detached at the edges in the presence of moisture.
June 3, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Sprotte Needle, REF 33115131B w/ Intro 20 G x 3.5", distributed by Teleflex Medical The SPROTTE lumbar puncture needl
Hazard: Teleflex received the attached Medical Device Recall Notice from Pajunk Medical. Teleflex Medical is a distributor of Pajunk products. According to the notice, Pajunk internally identified a packaging problem that may affect certain batches of the SPROTTE lumbar puncture cannulas with introducer. Due to this problem Pajunk cannot guarantee the sterility of the affected batches.
June 3, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Sprotte Needle, REF 32115130C w/ Intro 22 G x 3.5", distributed by Teleflex Medical The SPROTTE lumbar puncture needl
Hazard: Teleflex received the attached Medical Device Recall Notice from Pajunk Medical. Teleflex Medical is a distributor of Pajunk products. According to the notice, Pajunk internally identified a packaging problem that may affect certain batches of the SPROTTE lumbar puncture cannulas with introducer. Due to this problem Pajunk cannot guarantee the sterility of the affected batches.
February 26, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Teleflex Medical Disposable Aortic Punch, in the following sizes: a) 2.8 mm, REF DP-28K b) 3.6 mm, REF DP-36K c) 4.0
Hazard: There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
February 26, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Hazard: There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
February 19, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
Hazard: The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
February 19, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
Hazard: The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.
February 19, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port, REF 2414, humidifier nebulizer kit
Hazard: There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.
February 19, 2020Medical DevicesFDA
TELEFLEX MEDICAL INC recalls HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit
Hazard: There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column during high flow oxygen therapy.