Teleflex Medical: 114 recalls on record

Recalls filed with 1 agency: FDA (114).

First recall on record: July 25, 2012. Most recent: September 18, 2019.

Risk classification: Class I: 20 · Class II: 91 · Class III: 3

Most recent recalls

DateAgencyProduct
September 18, 2019FDAHudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, …Z-2313-2019
September 18, 2019FDAHudson RCI Sheridan/HVT: a) 5.0 mm, REF 5-10310 b) 5.5 mm, REF 5-10311 c) 6.0 mm, REF …Z-2316-2019
June 26, 2019FDAHudson RCI Sheridan: 1) HVT 6.0 mm, Product Code 5-10312 2) HVT 6.5 mm, Product Code 5-…Z-1764-2019
June 5, 2019FDARUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0Z-1683-2019
November 15, 2017FDAWECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R) Clip Applier, REF AE05ML (IPN…Z-0083-2018
October 25, 2017FDAPilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e…Z-0039-2018
October 4, 2017FDAPercuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with 5mm attachmen…Z-3219-2017
October 4, 2017FDAPercuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attach…Z-3222-2017
June 21, 2017FDASheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured …Z-2587-2017
June 14, 2017FDAHudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,Z-2251-2017
May 31, 2017FDAPE CONNECTOR 3/8 Y 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Acc…Z-2128-2017
May 31, 2017FDAPE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connec…Z-2127-2017
May 24, 2017FDAWECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat i…Z-2108-2017
April 26, 2017FDAArrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.Z-1829-2017
February 15, 2017FDASheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tub…Z-1177-2017
December 28, 2016FDAMucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe …Z-0898-2017
December 7, 2016FDAARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured for: Telef…Z-0675-2017
October 26, 2016FDAWilly Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particu…Z-0044-2017
September 7, 2016FDAMAQUET Servo Humidifier 163, Inmed Mfg. Sdn. Bhd. Lot PT 2577, Jalan Perusahaan, 4, 34600…Z-2683-2016
August 17, 2016FDAServo Humidifier 163, Model 01-06-8125-8, REF 6419365 Product Usage: A heat and moist…Z-2374-2016
May 4, 2016FDAPleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only,…Z-1582-2016
November 25, 2015FDATaut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93. To provide an access port into the…Z-0277-2016
August 26, 2015FDAHUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Right sided), Sizes: 28 Fr., 35 F…Z-2368-2015
February 18, 2015FDAAQUAPAK 340 SW, 340, ML W/040, ADAPTOR, JAPA. Product Usage: The Humidifier Adaptor i…Z-1101-2015
December 24, 2014FDAWECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are int…Z-0826-2015

Questions about this company

How many recalls does Teleflex Medical have?
Recalert has 114 U.S. recalls on record for Teleflex Medical, published between July 25, 2012 and September 18, 2019.
What was the most recent Teleflex Medical recall?
FDA recall Z-2313-2019, published September 18, 2019: Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514 d) 7.5 mm, REF 5-22515 e) 8.0 mm, REF 5-22516 f) 8.5 mm, REF 5-22517 g) 9.0 mm, REF 5-22518 h…
Which agencies have handled Teleflex Medical recalls?
Teleflex Medical appears as the recalling firm in recalls from: FDA (114).

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