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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.
December 28, 2016Medical DevicesFDA
Teleflex Medical recalls Mucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe and Vial Adapter; Product Code
Hazard: Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
December 28, 2016Medical DevicesFDA
Teleflex Medical recalls RUSCH, Pocket PAC IC Intermittent Cath Kit, 8 FR, 12 FR, 14 FR, 10 FR and 16 FR, Rx Only, Sterile, Intermittent self-
Hazard: Labeling Inconsistency: The products have been labeled with the incorrect expiration date which exceeds the actual, validated 35-month shelf life.
December 28, 2016Medical DevicesFDA
Teleflex Medical recalls LMA MADdy, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized s
Hazard: Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
December 28, 2016Medical DevicesFDA
Teleflex Medical recalls LMA MADett, Endotracheal tube Mucosal Atomization Device, Rx only, Product Usage: These products are used for the d
Hazard: Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
December 28, 2016Medical DevicesFDA
Teleflex Medical recalls LMA MADgic, Atomization Device with 3mL Syringe, Rx only, Product Usage: These products are used for the delivery o
Hazard: Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
December 28, 2016Medical DevicesFDA
Teleflex Medical recalls FLEXI NOZZLE SHORT Product Usage: These products are used for the delivery of topical anesthesia via an atomized spr
Hazard: Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
December 28, 2016Medical DevicesFDA
Teleflex Medical recalls FLEXI NOZZLE LONG, 10 Boxes of 25 units each Product Usage: These products are used for the delivery of topical anes
Hazard: Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
December 28, 2016Medical DevicesFDA
Teleflex Medical recalls LMA MADomizer, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomiz
Hazard: Product Defect; These products may produce a straight stream instead of a fully atomized plume of medication.
December 21, 2016Medical DevicesFDA
Teleflex Medical recalls WECK Visistat 35W, Disposable Skin Stapler, Rx Only, Sterile, Teleflex Medical, NC 27709. The intended use of the Vi
Hazard: Sterility Deficiency: The packages are not sealed properly and thus the sterility is not assured.
December 21, 2016Medical DevicesFDA
Teleflex Medical recalls Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous s
Hazard: The devices wings may become partially detached from the EFx Shield during use.
December 7, 2016Medical DevicesFDA
Teleflex Medical recalls ARROW OnControl Ported Aspiration System Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is in
Hazard: Sterility: Due to a potential incomplete seal on the outer sterile package.
December 7, 2016Medical DevicesFDA
Teleflex Medical recalls OnControl Biopsy System Ported Needle Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is inten
Hazard: Sterility: Due to a potential incomplete seal on the outer sterile package.
December 7, 2016Medical DevicesFDA
Teleflex Medical recalls ARROW OnControl Bone Lesion Biopsy System Tray, Sterile, Rx only, The Arrow OnControl Bone Lesion Biopsy System is inte
Hazard: Sterility: Due to a potential incomplete seal on the outer sterile package.
December 7, 2016Medical DevicesFDA
Teleflex Medical recalls ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray, Sterile, The Arrow OnControl Bone Marrow Aspiration System
Hazard: Sterility: Due to a potential incomplete seal on the outer sterile package.
December 7, 2016Medical DevicesFDA
Teleflex Medical recalls ARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured for: Teleflex Medical, The Arrow OnCon
Hazard: Sterility: Due to a potential incomplete seal on the outer sterile package.
October 26, 2016Medical DevicesFDA
Teleflex Medical recalls Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow t
Hazard: The connector may disconnect from the tracheostomy tube during use.
October 19, 2016Medical DevicesFDA
Teleflex Medical recalls Teleflex Percuaneous Solutions, Johans Grasper, Ref ML004EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park, N
Hazard: The product is being recalled due to a labeling error. The Gripper Graspers are labeled as Johans Graspers and the Johans Graspers are labeled as Gripper Graspers.
October 19, 2016Medical DevicesFDA
Teleflex Medical recalls Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park,
Hazard: The product is being recalled due to a labeling error. The Gripper Graspers are labeled as Johans Graspers and the Johans Graspers are labeled as Gripper Graspers.
September 14, 2016Medical DevicesFDA
Teleflex Medical recalls WECK¿ Horizon" Manual-Load Ligating Clip Applier, For Medium-Large Size Horizon Ligation Clips Curved Jaw, 11 (28cm), R
Hazard: Misbranded: Incorrect etching on the device.
September 7, 2016Medical DevicesFDA
Teleflex Medical recalls MAQUET Servo Humidifier 163, Inmed Mfg. Sdn. Bhd. Lot PT 2577, Jalan Perusahaan, 4, 34600 Kamunting, Perak, Malaysia.
Hazard: Cracking may occur at the 15mm and 22mm ISO female connector.
August 24, 2016Medical DevicesFDA
Teleflex Medical recalls Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and withdr
Hazard: Incorrect expiration date was printed on the product label.
August 17, 2016Medical DevicesFDA
Teleflex Medical recalls Servo Humidifier 163, Model 01-06-8125-8, REF 6419365 Product Usage: A heat and moisture condenser (artifical nose)
Hazard: Cracks may occur at the 15mm and 22mm ISO female connector.
August 10, 2016Medical DevicesFDA
Teleflex Medical recalls Horizon 24 Large Titanium Clips with Adhesive Backing, Ref 004204, Rx Only, Sterile. The metal ligating clips are int
Hazard: The manufacturing and expiration dates are not printed on the blister pack label.
June 15, 2016Medical DevicesFDA
Teleflex Medical recalls Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex In
Hazard: The labeling of some units indicates that it contains a size 7mm tracheal tube, but may contain a size 7.5mm tracheal tube.
May 4, 2016Medical DevicesFDA
Teleflex Medical recalls Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product U
Hazard: The label on the Tyvek bag is missing. This is used by customers to identify material code, lot number, and expiration date once the product is removed from the shipper box.
March 23, 2016Medical DevicesFDA
Teleflex Medical recalls Pilling Modular Verres Body/Obturator, Product Code 140880
Hazard: Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).
March 2, 2016Medical DevicesFDA
Teleflex Medical recalls Auto Endo5 Hem-o-lok Automatic Clip Applier, Medium Large Polymer Clips, Rx Only, Sterile, REF 543965 Product Usage:
Hazard: The clip in the applier may be missing a boss. A boss is the part of the clip that is used to hold the clip within the applier jaws prior to application.
December 23, 2015Medical DevicesFDA
Teleflex Medical recalls Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column
Hazard: Product is being recalled due to complaints that the inspiratory and expiratory tubes are transposed.
November 25, 2015Medical DevicesFDA
Teleflex Medical recalls Taut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93. To provide an access port into the peritoneal cavity.
Hazard: The defective component can cause gas leakage through the device. This can result in loss of pneumoperitoneum, potentially necessitating removal of the defective device and insertion of another device.
November 18, 2015Medical DevicesFDA
Teleflex Medical recalls Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical.
Hazard: Due to reports of the plastic coating of the stylet splitting and/or breaking off of the stylet.