Convenience Kit Correction

6 recalls on record · Last recall: Aug 3, 2026

Safety Score

83/100

Good

Based on recall frequency and severity over the past 3 years, with older recalls weighted less.

Severity Breakdown

Class I — Serious

Class II — Moderate

Class III — Low Risk

Unclassified

Recall Timeline

FDAAug 3, 2026

Convenience Kit Correction: Medical Action Industries Issues Correction for Kits Containing Recalled Namic Manifolds

Particulates have the potential to be introduced into blood circulation and become lodged within blood vessels.

FDAAug 3, 2026

Convenience Kit Correction: Medline Issues Correction for Kits Containing Huons Lidocaine Hydrochloride and Bupivacaine Hydrochloride in Dextrose Injection

Medline is correcting affected convenience kits by removing recalled Lidocaine Hydrochloride and Bupivacaine Hydrochloride in Dextrose Injection components from affected convenience kits.

FDAJul 30, 2026

Convenience Kit Correction: Argon Medical Issues Correction for Convenience Kits Containing Spectra Medical Device Lidocaine Ampules

Argon Medical is correcting affected convenience kits by removing included Spectra Medical Devices Lidocaine Ampules.

FDAJul 16, 2026

Convenience Kit Correction: Arrow International Issues Correction for Convenience Kits Containing Recalled Huons Lidocaine and Bupivacaine and Saline

Saline, Lidocaine and Bupivacaine from affected convenience kits should not be used.

FDAJul 6, 2026

Convenience Kit Correction: Windstone Medical Packaging, Inc. Issues Correction for Convenience Kit

Certain Cardinal Health Webcol Large Alcohol Prep Pads in Custom Convenience Kits manufactured by Aligned Medical Solutions are not sterile.

FDAJun 12, 2026

Convenience Kit Correction: Medline Issues Correction for Kits Containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP

Medline is correcting affected convenience kits by removing recalled Bupivacaine Hydrochloride in Dextrose Injection components.

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