TELEFLEX MEDICAL INC recalls
Every recall we track for TELEFLEX MEDICAL INC — 32 in all, from 2019–2022 — plus the complaints and injury reports the public filed about them. 3 are rated “stop using now”.
Recalls per year, by danger level
Recalls from TELEFLEX MEDICAL INC peaked in 2020 (15); 32 since 2017. 9% rated “stop using now”.
All FDA recall records for TELEFLEX MEDICAL INC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 1 | 2 | 3 | 0 | 6 |
| 2020 | 2 | 8 | 5 | 0 | 15 |
| 2021 | 0 | 1 | 1 | 0 | 2 |
| 2022 | 0 | 7 | 2 | 0 | 9 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for TELEFLEX MEDICAL INC recalls
What to do if you have a recalled TELEFLEX MEDICAL INC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All TELEFLEX MEDICAL INC recalls
12 shown- Lower riskMedical device
TELEFLEX MEDICAL INC recalls (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,
Gibeck Humid-Vent 2S Flex DC humidifiers with specific product numbers (17731, 17732, 19061, 19062, 19812) have reported torn corrugated breathing tubes. Consumers should check their product numbers against the list provided.
GibeckApr 11, 2022 - Use cautionMedical device
TELEFLEX MEDICAL INC recalls Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-W containing component:
Arrow recalls specific Percutaneous Thrombolytic Device kits (PTD) with potential tip separation during use. Affected units include certain lot numbers and model codes. Stop using immediately if you own these kits.
ArrowJan 11, 2022 - Use cautionMedical device
TELEFLEX MEDICAL INC recalls RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is
Teleflex recalls Polaris laryngoscopes with cracks or breaks at the hinge due to customer reports. Models 44401-44403 with specific lots are affected. Stop using if you have these items.
TeleflexFeb 18, 2021 - Lower riskMedical device
TELEFLEX MEDICAL INC recalls PLEUR-EVAC Thoracic Catheters (CATHETER, IRRIGATION). The thoracic catheter is a sterile, non pyrogenic, single use
Teleflex recalls sterile thoracic catheters due to lack of sterility assurance. Affected units may cause infections if used without proper sterility.
TeleflexFeb 12, 2021 - Lower riskMedical device
TELEFLEX MEDICAL INC recalls Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical
Teleflex Medical recalls Pleur-evac Thoracic Catheters (DTRC-20S) due to potential sterility issues. These catheters are used in surgical procedures for chest drainage and must be used within 30 days.
Teleflex MedicalAug 7, 2020 - Use cautionMedical device
TELEFLEX MEDICAL INC recalls Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device
Teleflex Medical recalls Rusch Greenlite laryngoscopes with specific product codes due to potential breaking at welded joints during use, which could lead to injury during tracheal intubation procedures.
Teleflex MedicalJul 6, 2020 - Lower riskMedical device
TELEFLEX MEDICAL INC recalls Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST DRAINAGE: To evacuate air
Teleflex Medical recalls Pleur-Evac Adult-Ped Wet chest drainage systems due to potential sterile packaging compromise. Affected units have specific lot numbers. Consumers should check their product details.
Teleflex MedicalJun 30, 2020 - Use cautionMedical device
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
Teleflex recalls RUSCH LASERTUBE rubber tubes for possible laser guard foil detachment in moisture, risking exposure during surgery. Affected units include specific sizes and lot numbers for tracheal intubation use.
TeleflexMay 29, 2020 - Stop using nowMedical device
TELEFLEX MEDICAL INC recalls Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Teleflex Medical recalls Pilling Aortic Punch 4.0mm Standard Tip (REF 353440) due to potential packaging compromise affecting sterility. Affected units sold with lot number 74B1500674.
Teleflex MedicalJan 13, 2020 - Use cautionMedical device
TELEFLEX MEDICAL INC recalls Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
Teleflex Medical recalls Rusch Green: Single-use metal laryngoscope blades that may break at welded joints, causing injury during patient use. Affected items have specific product codes and lot numbers.
Teleflex MedicalJan 9, 2020 - Stop using nowMedical device
TELEFLEX MEDICAL INC recalls HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit
Teleflex Medical recalls the HUDSON RCI Comfort Flo Humidification System (REF 2410) due to potential water flooding in the circuit during high-flow oxygen therapy.
Teleflex MedicalDec 13, 2019 - Lower riskMedical device
TELEFLEX MEDICAL INC recalls Sprotte Needle, REF 32115130C w/ Intro 22 G x 3.5", distributed by Teleflex Medical The SPROTTE lumbar puncture needles
Teleflex Medical recalls Sprotte lumbar puncture needles with specific batch numbers due to potential packaging issues that may compromise sterility. Affected users should contact Teleflex for details.
Teleflex MedicalOct 11, 2019
TELEFLEX MEDICAL INC recall questions
How many recalls has TELEFLEX MEDICAL INC had?
32 recalls from TELEFLEX MEDICAL INC are on record with U.S. safety agencies, from 2019–2022.
What is the most recent TELEFLEX MEDICAL INC recall?
TELEFLEX MEDICAL INC recalls (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,, dated Apr 11, 2022. Every TELEFLEX MEDICAL INC recall is listed on this page, newest first.
Why are TELEFLEX MEDICAL INC products recalled?
The most common reasons on record: Breaking at the point of a welded joint (7); The firm received reports indicating PTD tip separation during use. (7); Potential for sterile packaging to be compromised¿ (2); Reports received of torn corrugated breathing tubes. (2).
What should I do if I have a recalled TELEFLEX MEDICAL INC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new TELEFLEX MEDICAL INC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.