Home › ANDERSEN PRODUCTS, INC. › AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Indivi

AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Indivi

ANDERSEN PRODUCTS, INC. · Model AN22.00 · UDI-DI 05060171440352

KNT

510(k) clearances

25,839

Adverse events (628 deaths)

268

Recalls

228

Facilities

Description

AN22 - Andersen Miller-Abbott Type Intestinal Tube, 16 Fr., Pre-Weighted (Individual)

Recalls

Date	Firm	Reason
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
2026-04-30	Avanos Medical, Inc.	Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.