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Kangaroo

Cardinal Health, Inc. · Model 460836E · UDI-DI 20884521742151

KNT PIF Prescription

510(k) clearances

26,153

Adverse events (631 deaths)

268

Recalls

228

Facilities

Description

Feeding Tube with IRIS Technology. For use with ENFit Connection System. Contains one (1) Stylet per Feeding Tube. ENFit is a federally registered trademark in multiple jurisdictions throughout the wo

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.