Recall Z-0366-2014— Teleflex Medical
Class II · Terminated
Class II FDA medical device recall by Teleflex Medical, initiated 2013-10-15, terminated 2015-11-04. FDA's recall record names no specific 510(k) clearance for this event. Product: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to visualize upper airway and aid in placement of tracheal tube.. Reason: Labeling inconsistency.
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-10-15
- Terminated
- 2015-11-04
- Firm location
- Durham, NC, United States
Product description
Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to visualize upper airway and aid in placement of tracheal tube.
Reason for recall
Labeling inconsistency
Data sourced from openFDA. This site is unofficial and independent of the FDA.