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AbbVie J

ABBVIE INC. · Model AV062 · UDI-DI 08054083014432

KNT Prescription
1
510(k) clearances
26,153
Adverse events (631 deaths)
268
Recalls
228
Facilities

Description

The AbbVie J is a 9 FR intestinal (J) tube, 120 cm in length. AbbVie J Tube for 15 FR PEG kit (List Number 62918-001) AbbVie J Tube for 20 FR PEG kit (List Number 0AV062-001) This kit includes (Fig. 1): - AbbVie J Tube with Teflon coated Guide Wire and Blue Guide Wire Lock - Y-Connector for the 15 FR PEG or 20 FR PEG - Fixation Screw (blue: 15 FR or violet: 20 FR) with Outer Ring - Click Adaptor consisting of: - Click Adaptor Cap - Click Adaptor Connector

Recalls

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