Medical DeviceApr 6, 2022
Avanos Medical BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French recall — FDA Z-0846-2022
Product was distributed with incorrect expiration date.
Class IIFDA: TerminatedAvanos Medical, Inc.
Recall history in this database
Classification mix: Class II: 15, Class I: 13, Class III: 3.
Medical DeviceApr 6, 2022
Avanos Medical BALLARD* Multi-Access Port (MAP) Catheter, Double Swivel Y- Adult, 16 French recall — FDA Z-0847-2022
Product was distributed with incorrect expiration date.
Class IIFDA: TerminatedAvanos Medical, Inc.
Medical DeviceApr 6, 2022
Avanos Medical BALLARD* Seal Cassette Replacement MAP - BALLARD* Seal Cassette Replacement recall — FDA Z-0845-2022
Product was distributed with incorrect expiration date.
Class IIFDA: TerminatedAvanos Medical, Inc.
Medical DeviceMay 6, 2020
Avanos Medical CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit recall — FDA Z-1822-2020
The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted.
Class IIFDA: TerminatedAvanos Medical, Inc.
Medical DeviceJan 15, 2020
Avanos Medical Haylard Closed Suction System for Neonates/Pediatrics, 5 Fr, 1 recall — FDA Z-0788-2020
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…
Class IIFDA: TerminatedAvanos Medical, Inc.
Medical DeviceNov 20, 2019
Avanos Medical CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG recall — FDA Z-0371-2020
The connector piece to the PEG tube does not pass over the guidewire.
Class IIFDA: TerminatedAvanos Medical, Inc.
Medical DeviceNov 20, 2019
Avanos Medical CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG recall — FDA Z-0370-2020
The connector piece to the PEG tube does not pass over the guidewire.
Class IIFDA: TerminatedAvanos Medical, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Avanos Medical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.