Overview of recall records associated with Avanos Medical, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 15, Class I: 13, Class III: 3.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
The IFU was missing some risk information requested by another country to be contained in the IFU pertaining to potential complications.
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled syringe subsequently recalled by Nurse Assist.
MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled syringe subsequently recalled by Nurse Assist.
Certain lots of BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI were labeled as not being made with Di(2-ethylhexyl) phthalate (DEHP); however, Avanos has determined that the…
Avanos has received an increase in complaints from customers for COOLIEF RF Generators producing F100 and F101 faults.
Potential for product manifold to crack during use on patients, possibly causing leaks in the respiratory circuit and can lead to the patient receiving inadequate ventilation.
Potential for product manifold to crack during use on patients, possibly causing leaks in the respiratory circuit and can lead to the patient receiving inadequate ventilation.
Sterile extension sets were distributed without an expiration date
Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately. CONFIRM placement of the NG/NI tube per institution protocol.
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.
