Recall Z-0846-2022— Avanos Medical, Inc.
Class II · Terminated
Class II FDA medical device recall by Avanos Medical, Inc., initiated 2021-11-22, terminated 2023-01-31. FDA's recall record names no specific 510(k) clearance for this event. Product: BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use. Reason: Product was distributed with incorrect expiration date..
- Recalling firm
- Avanos Medical, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-11-22
- Terminated
- 2023-01-31
- Firm location
- Alpharetta, GA, United States
Product description
BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use
Reason for recall
Product was distributed with incorrect expiration date.
Data sourced from openFDA. This site is unofficial and independent of the FDA.