BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics, Elbow Manifold. — FDA record Z-1190-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 3, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics, Elbow Manifold.
Reason
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.
Classification
Class I
Recalling firm
Avanos Medical, Inc.
Quantity
220 units
Agency-reported status
Terminated
Source record identifier
Z-1190-2023

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityAll lots are affected. Stock Code (Lot Number): B50511 (20098277), B50611 (20098278), B50711 (20098279), B50811 (20097177, 20097177R1).

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the state of Oklahoma.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Mar 22, 2023
Recall initiation date
Feb 3, 2023
Center classification date
Mar 13, 2023
Termination date
Sep 5, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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