Recall Z-2724-2020— Medline Industries Inc
Class II · Ongoing
Class II FDA medical device recall by Medline Industries Inc, initiated 2020-06-30. FDA's recall record names no specific 510(k) clearance for this event. Product: ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.. Reason: There are reports of the suction catheter coming apart from the device assembly during use..
- Recalling firm
- Medline Industries Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2020-06-30
- Firm location
- Northfield, IL, United States
Product description
ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
Reason for recall
There are reports of the suction catheter coming apart from the device assembly during use.
Data sourced from openFDA. This site is unofficial and independent of the FDA.