Manufacturer

Teleflex Medical

204 recalls in our database name Teleflex Medical as the manufacturing or recalling firm.

What the numbers show

Total: 204
Critical: 9
Severe: 8
Most recent: 2020-01-22

Of the 204 recalls from Teleflex Medical we have scored against our rubric, 9 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 8 (4%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

101–125 of 204

HighFDA (Devices)·Z-1109-2015·2015-02-18
Teleflex Medical Recalls Aquapak 640 SW Humidifier Adaptors for Foreign Material
Teleflex Medical is recalling Aquapak 640 SW humidifier adaptors because packages may contain black particles. The recall covers 15,779,607 units distributed worldwide.
Product
AQUAPAK 640 SW, 650ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor pac
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1097-2015·2015-02-18
Teleflex Medical Recalls Aquapak 340 SW Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUAPAK 340 SW, 340 ML W/404 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1107-2015·2015-02-18
Teleflex Medical Recalls 040 Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling 040 Humidifier Adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
ADAPTOR, 040 HUM, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with the wate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1102-2015·2015-02-18
Teleflex Medical Recalls Aqua 540 Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling Aqua 540 Humidifier Adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUA 540 SW, 540 W/040 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1098-2015·2015-02-18
Teleflex Medical Recalls Aquapak 340 SW Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUAPAK 340 SW, 340 ML W/040B ADAPTOR, BRI Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor pac
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1096-2015·2015-02-18
Teleflex Medical Recalls Aquapak 101 SW Humidifier Adaptors for Foreign Material
Teleflex Medical is recalling Aquapak 101 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUAPAK 101 SW, 190ML W/040 ADAPTOR, JAPA Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1106-2015·2015-02-18
Teleflex Medical Recalls Aquapak 640 SW Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling Aquapak 640 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUAPAK 640 SW, 650ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor pac
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1103-2015·2015-02-18
Teleflex Medical Recalls AQUAPAK 640 SW Humidifier Adaptors for Foreign Material
Teleflex Medical is recalling AQUAPAK 640 SW humidifier adaptors because packages may contain black particles. The recall covers 15,779,607 units distributed worldwide.
Product
AQUAPAK 640 SW, 650ML W/040 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1104-2015·2015-02-18
Teleflex Medical Recalls Aquapak Sterile Water Adaptors for Foreign Material
Teleflex Medical is recalling Aquapak sterile water humidifier adaptors because packages may contain black particles.
Product
AQUAPAK SW/EAU STERILE, 650 ML W/ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor pack
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1085-2015·2015-02-18
Teleflex Recalls LMA Supreme Size 5 Due to Potential Size 4 Mislabeling
Teleflex Medical is recalling 2,640 units of LMA Supreme (New Cuff) Size 5 devices because some may be mislabeled as Size 5 but are actually Size 4.
Product
LMA (Laryngeal Mask Airway) Supreme (New Cuff) Size 5, Sterile, Single use, Product Usage: Achieve and maintain control of airway during routine anaesthesia in fasted patient using either spontaneous or positive pressure ventilation, cardiopulmonary resuscitation, the faile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1108-2015·2015-02-18
Teleflex Medical Recalls Aquapak 340 SW Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUAPAK 340 SW, 340ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor pac
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1078-2015·2015-02-18
Teleflex Recalls Preformed Tracheal Tubes Due to Incorrect Labeling
Teleflex Medical is recalling 300 units of preformed tracheal tubes because they are incorrectly labeled as cuffed oral tubes instead of uncuffed nasal tubes.
Product
Hudson RCI, Sheridan, Preformed Tracheal Tubes, Cuffed and Uncuffed, Rx Only, Sterile, Teleflex Medical.
Category
Medical Device
Distribution
12 states
ModerateFDA (Devices)·Z-1105-2015·2015-02-18
Teleflex Medical Recalls Aquapak 640 SW Humidifier Adaptors
Teleflex Medical is recalling Aquapak 640 SW humidifier adaptors because packages may contain foreign material, specifically black particles.
Product
AQUAPAK 640 SW, 650ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor pac
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1095-2015·2015-02-18
Teleflex Recalls Hudson RCI Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling specific Hudson RCI Humidifier Adaptors because the packages may contain black particles. The recall affects units distributed worldwide.
Product
Hudson RCI¿ Humidifier Adaptor, 040 contained in the following units: HUMIDIFIER ADAPTOR 040 Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0799-2015·2014-12-24
Teleflex Recalls Sheridan Cuffed Tracheal Tubes Due to Labeling Error
Teleflex Medical is recalling 14,000 Sheridan/CF Cuffed Tracheal Tubes because the label indicates size 8mm but the tube may be size 7.5mm.
Product
Sheridan/CF Cuffed Tracheal Tube, Sterile, Rx only, Teleflex Medical, Research Triangle Park, NC 27708. Designed for oral and nasal intubation and are indicated for airway management.
Category
Medical Device
Distribution
0 states
LowFDA (Devices)·Z-0826-2015·2014-12-24
Teleflex Recalls Weck Hemoclip Ligating Clips Due to Labeling Error
Teleflex Medical is recalling 3,180 units of Weck Hemoclip Ligating Clips because manufacturing and expiration dates were transposed on the packaging labels.
Product
WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0504-2015·2014-12-10
Teleflex Medical Recalls Aquapak Nebulizer Adaptors Due to Sterility Concerns
Teleflex Medical is recalling Aquapak Nebulizer Adaptors because packaging seals may be open or weak, potentially compromising the sterility of the devices.
Product
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak Nebulizer Adaptor 028, Sterile, Shelfpak, Product No. 031-28 & 031-28F, Aqaupak Nebulizer Adaptor 033, Sterile, Shelfpak, Product No. 031-33; Aqaupak Nebulizer Adaptor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0505-2015·2014-12-10
Teleflex Medical Recalls Aquapak Nebulizer Adaptors Due to Seal Integrity Concerns
Teleflex Medical is recalling Aquapak nebulizer adaptors because packaging seals may be open or weak, potentially affecting the sterility of the device.
Product
Aqauapak 728 SW, 760 ML W/028 Adaptor, Intl, Product No. 403728; Aqauapak 1028 SW, 1070 ML/W028 Adaptor, Intl, Product No. 404128; Aqauapak 428 SW, 440 ML W/028 Adaptor, Intl, Product No. 404428; Aquapak 728 SW, 760 ML W/028 Adaptor, Product No. 037-28; Aquapak SW/EAU Sterile, 76
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2714-2014·2014-10-08
Teleflex Recalls Hudson Pediatric Anesthesia Breathing Circuits Due to Cracking
Teleflex Medical is recalling Hudson RCI Pediatric Anesthesia Breathing Circuits because they can crack prior to and during use.
Product
Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Ypiece.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2661-2014·2014-09-24
Teleflex Recalls Soft Rubber Bladder Catheters Due to Missing Latex Warning
Teleflex Medical is recalling sterile soft rubber bladder catheters because the product labels failed to include a Natural Rubber Latex caution statement.
Product
Rusch, Soft Rubber (Nelaton and Nelaton Robinson), Bladder Catheter, Sterile. These catheters are indicated for the routine drainage of urine from the bladder. These catheters are not intended or designed for indwelling use.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2154-2014·2014-08-13
Teleflex Recalls RUSCH Foley Urinary Catheter Insertion Trays Due to Labeling Error
Teleflex Medical is recalling 720 RUSCH Foley Urinary Catheter Insertion Trays because the expiration date is incorrectly printed as the same as the manufacturing date.
Product
RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe, BZK Swabs, Sterile, Rx only, Teleflex Medical Product Code: 76730.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2130-2014·2014-08-06
Teleflex Recalls RUSCH TruLite Disposable Laryngoscope Handles
Teleflex Medical is recalling RUSCH TruLite laryngoscope handles because the handle may heat up and melt the end cap.
Product
RUSCH, TruLite, One-Piece Disposable Laryngoscope Handle Blade Combination, Non-Sterile, Rx Only, Distributed by: Teleflex Medical.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2119-2014·2014-08-06
Teleflex Medical Recalls Emerald Fiberoptic Blades Due to Packaging Error
Teleflex Medical is recalling 120 units of Emerald Fiberoptic Blades because the boxes contained incorrect Miller 4 blades instead of the labeled Macintosh 4 blades.
Product
Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize a patient's upper airway and aid placement of a tracheal tube.
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-2108-2014·2014-07-30
Teleflex Recalls Hudson RCI Breathing Circuits Due to Temperature Probe Defect
Teleflex Medical is recalling Hudson RCI breathing circuits because the temperature probe does not properly connect to the temperature port.
Product
Hudson RCI, Breathing Circuit, Adult Single Limb (W/Connector, Adaptor, Y Piece), Rx Only, Single Patient Use. The Hudson Heated Wire Ventilator Circuit is intended as a conduit for respiratory gas between a patient and a ventilator, and includes heated wires for use with a Conch
Category
Medical Device
Distribution
16 states
ModerateFDA (Devices)·Z-2107-2014·2014-07-30
Teleflex Recalls Hudson RCI Breathing Circuits Due to Temperature Probe Defect
Teleflex Medical is recalling 11,679 Hudson RCI Breathing Circuits because the temperature probe does not properly connect to the temperature port.
Product
Hudson RCI, Breathing Circuit, Adult, Single Limb w/Heated Wire, [Respiratory Gas Humidifier, (Direct Patient Interface)]. The Hudson Heated Wire Ventilator Circuit is intended as a conduit for respiratory gas between a patient and a ventilator, and includes heated wires for use
Category
Medical Device
Distribution
16 states

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

Teleflex Medical

Czech company

Country: Czech Republic

Source: Wikidata (Q121622528), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.