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TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC Recalls

All product recalls associated with TELEFLEX MEDICAL INC.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Apr 2022

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–20 of 21 recalls

TELEFLEX MEDICAL INC: (1) Teleflex Flex tube, Product #20011, sterile; (2) Tele...

Reports received of torn corrugated breathing tubes.

FDAApr 11, 2022Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile...

Reports received of torn corrugated breathing tubes.

FDAApr 11, 2022Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: 5 Fr. X 65 cm Arrow-Trerotola PTD Kit, Percutaneous Throm...

The firm received reports indicating PTD tip separation during use.

FDAJan 11, 2022Nationwide• TELEFLEX MEDICAL INC

Page 1 of 2Next

TELEFLEX MEDICAL INC: Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device...

The firm received reports indicating PTD tip separation during use.

FDAJan 11, 2022Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Throm...

The firm received reports indicating PTD tip separation during use.

FDAJan 11, 2022Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: RUSCH POLARIS" Laryngoscope - Product Usage: intended to ...

Teleflex is voluntarily recalling the products referenced above due to customers reporting that the laryngoscope handles develop cracks and/or break at the hinge.

FDAFeb 18, 2021Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: PLEUR-EVAC Thoracic Catheters (CATHETER, IRRIGATION). The...

Teleflex is recalling this product due to a lack of assurance of sterility.

FDAFeb 12, 2021Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The t...

Potential sterility issue

FDAAug 7, 2020AZ, AR, CA +24 more• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Rusch Greenlite Product Code: 004550002 GTIN: 14026704663...

Breaking at the point of a welded joint

FDAJul 6, 2020Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Pleur-Evac Adult-Ped Wet, LF Intl Eng, product code: A-80...

Potential for sterile packaging to be compromised

FDAJun 30, 2020Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A...

Potential for sterile packaging to be compromised

FDAJun 30, 2020Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4...

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.

FDAMay 29, 2020Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Teleflex Medical Disposable Aortic Punch, in the followin...

There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.

FDAJan 13, 2020Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440

There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.

FDAJan 13, 2020Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Rusch Greenlite Single-Use Metal Laryngoscope Blade for F...

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.

FDAJan 9, 2020Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: HUDSON RCI COMFORT FLO Humidification System, REF 2410, h...

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.

FDADec 13, 2019Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: HUDSON RCI COMFORT FLO Corrugated Humidification System, ...

FDADec 13, 2019Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Sprotte Needle, REF 32115130C w/ Intro 22 G x 3.5", distr...

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.

FDAOct 11, 2019Nationwide• TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC: Sprotte Needle, REF 33115131B w/ Intro 20 G x 3.5", distr...

FDAOct 11, 2019Nationwide• TELEFLEX MEDICAL INC

Teleflex Medical, Inc.: Latex-Free REF B1000, Belly Bag Urine Collection Bag with...

Firm received complaints of leaking urine collection bags.

FDAMay 13, 2004Nationwide• Teleflex Medical, Inc.