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Avanos Medical Recalls
57 recalls on record · November 20, 2019 to June 17, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog N
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog N
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog N
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catal
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catal
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catal
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Pr
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Pr
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Pr
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tu
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
June 17, 2026Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320
Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 22714183-5 Software Version: N/A Pr
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 227-5 Software Version: N/A Product
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 2271418-5 Software Version: N/A Pro
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 2210-5 Software Version: N/A Produc
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 220135 Software Version: N/A Produc
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 20083 Software Version: N/A Product
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 210 Software Version: N/A Product D
Hazard: Lack of sterility assurance for closed suction catheter systems
April 23, 2025Medical DevicesFDA
Avanos Medical, Inc. recalls Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 198 Software Version: N/A Product D
Hazard: Lack of sterility assurance for closed suction catheter systems
July 31, 2024Medical DevicesFDA
Avanos Medical, Inc. recalls MIC-KEY* Gastric-Jejunal Feeding Tube Kit, Endoscopic / Radiologic Placement, Low-Profile GJ-Tube, REF 0270xx (Non-ENFIT
Hazard: The IFU was missing some risk information requested by another country to be contained in the IFU pertaining to potential complications.
June 19, 2024Medical DevicesFDA
Avanos Medical, Inc. recalls NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product descriptions: a.0.5mL Oral Syringe Orange NonS
Hazard: The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.