Recall Z-0788-2020— Avanos Medical, Inc.
Class II · Terminated
Class II FDA medical device recall by Avanos Medical, Inc., initiated 2019-11-05, terminated 2023-08-16. FDA's recall record names no specific 510(k) clearance for this event. Product: Haylard Closed Suction System for Neonates/Pediatrics, 5 Fr, 1. REF 195, Y-Adapter, SAP Finished Product Code 109382303; 2. REF 201, with BALLARD Technology, SAP Finished Product Code 109382803; 3. REF 202, Elbow, SAP Finished Product Code 109382903; 4. REF 195-5 Y-Adapter, SAP Finished Product Code 109838302.. Reason: Avanos Medical has received reports stating that the central lumen of some 5 Fr Neonate/Pediatric Closed Suction Catheters may be fully blocked or partially blocked. This may cause the closed suction catheters (CSCs) to inadequately suction secretions and/or saline fluids form the patient's airway to prevent oxygen desaturation..
- Recalling firm
- Avanos Medical, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-11-05
- Terminated
- 2023-08-16
- Firm location
- Alpharetta, GA, United States
Product description
Haylard Closed Suction System for Neonates/Pediatrics, 5 Fr, 1. REF 195, Y-Adapter, SAP Finished Product Code 109382303; 2. REF 201, with BALLARD Technology, SAP Finished Product Code 109382803; 3. REF 202, Elbow, SAP Finished Product Code 109382903; 4. REF 195-5 Y-Adapter, SAP Finished Product Code 109838302.
Reason for recall
Avanos Medical has received reports stating that the central lumen of some 5 Fr Neonate/Pediatric Closed Suction Catheters may be fully blocked or partially blocked. This may cause the closed suction catheters (CSCs) to inadequately suction secretions and/or saline fluids form the patient's airway to prevent oxygen desaturation.
Data sourced from openFDA. This site is unofficial and independent of the FDA.