Teleflex Medical Recall

Teleflex Incorporated Announces Worldwide Recall of …

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teleflex-incorporated-announces-worldwide-recall-arrow-trerotolatm-over-wire-ptdr-kit-percutaneous

Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care and surgery, has announced a worldwide recall of Arrow-Trerotola™ Over-The-Wire PTD® Kit ...

Teleflex Recalls Iso-Gard Filter S for Risk of Splitting or …

https://www.fda.gov/medical-devices/medical-device-recalls/teleflex-recalls-iso-gard-filter-s-risk-splitting-or-detaching-may-cause-leakage-and-insufficient

Class 2 Device Recall Pleurevac - Food and Drug …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=183012

A customer service representative will contact you with a Return Goods Authorization (RGA) Number and will provide instructions for the return of products to …

Class 2 Device Recall Teleflex Medical RUSCH

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=196306

Teleflex sent an URGENT MEDICAL DEVICE notice to its consignees on 10/03/2022 by Fed Ex 2nd day. The notice explained the problem and the hazard and …

Teleflex - Teleflex Incorporated Announces Worldwide …

https://investors.teleflex.com/news/news-details/2021/Teleflex-Incorporated-Announces-Worldwide-Recall-of-Arrow-Trerotola-Over-The-Wire-PTD-Kit-Percutaneous-Thrombolytic-Device-7FR/default.aspx

WAYNE, Pa., Nov. 26, 2021 (GLOBE NEWSWIRE) - Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care and …

Teleflex Incorporated Announces Worldwide Recall of Arrow

https://finance.yahoo.com/news/teleflex-incorporated-announces-worldwide-recall-230000458.html

WAYNE, Pa., Nov. 26, 2021 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care and …

Teleflex - Teleflex Incorporated Announces Worldwide …

https://investors.teleflex.com/news/news-details/2020/Teleflex-Incorporated-Announces-Worldwide-Voluntary-Recall-of-COMFORT-FLO-Humidification-System/default.aspx

WAYNE, Pa., Feb. 14, 2020 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a global provider of medical technologies for critical care and surgery, has …

FDA Teleflex Recall Brings Back Over 6M Endotracheal Devices

https://www.yourlawyer.com/defective-medical-devices/fda-teleflex-recall/

According to the announcement released with the FDA Teleflex recall, disconnection from the breathing unit may result in insufficient oxygenation, suffocation, …

Urgent Medical Device Recall Notification - Teleflex

https://teleflex.com/global/product-areas/MAD_Atomization_Cust_Notif_and_Ack_Form.pdf

Page 1 of 2 Immediate Attention Requested Amended Recall Acknowledgment Form for: LMA® MAD Nasal™ Intranasal Mucosal Atomization Device Check the appropriate box …

Urgent Medical Device Recall Notification

https://ems.ohio.gov/static/links/emsRecallNotification11042016-2.pdf

(RGA) Number and will provide instructions for the return of product to Teleflex Medical. 3. If you have no affected stock, please complete the enclosed Recall Acknowledgment …