Recall Z-0245-2016— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2015-08-24, terminated 2017-09-25. FDA's recall record names no specific 510(k) clearance for this event. Product: R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip, Sterile, Rx only, Teleflex Medical.. Reason: Due to reports of the plastic coating of the stylet splitting and/or breaking off of the stylet..
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-08-24
- Terminated
- 2017-09-25
- Firm location
- Research Triangle Park, NC, United States
Product description
R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip, Sterile, Rx only, Teleflex Medical.
Reason for recall
Due to reports of the plastic coating of the stylet splitting and/or breaking off of the stylet.
Data sourced from openFDA. This site is unofficial and independent of the FDA.