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Convenience Kit Correction

11 recalls on record · Last recall: Sep 24, 2026

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Records, not a safety rating.

Recall counts do not account for sales volume, exposure or differences in reporting. Agency records can overlap. A low count does not establish that a brand or product is safe.

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Severity Breakdown

Class I — Serious
0
Class II — Moderate
0
Class III — Low Risk
0
Unclassified
11

Categories

MEDICATION

Recall Timeline

FDASep 24, 2026

Convenience Kit Correction: Becton Dickinson Issues Correction for Kits and Procedure Trays Containing Recalled Sodium Chloride Ampules

BD is correcting convenience kits and procedural trays containing recalled Huons Co. sodium chloride ampules

FDASep 21, 2026

Convenience Kit Correction: AVID Medical Issues Correction for Kits Containing Huons Sodium Chloride Ampules

AVID Medical is correcting convenience kits containing recalled Huons Co. sodium chloride ampules.

FDASep 2, 2026

Convenience Kit Correction: Medline Issues Correction for Convenience Kits Containing BD ChloraPrep Applicators

Certain BD ChloraPrep Applicators in Convenience Kits manufactured by Medline may not be sterile.

FDAAug 27, 2026

Convenience Kit Correction: AVID Medical Issues Correction for Kits Containing Medline Namic Star Off Handle Manifolds

AVID Medical is correcting convenience kits containing Manifolds affected by the Medline Namic Angiographic Star Off Handle Manifold Recall.

FDAAug 12, 2026

Convenience Kit Correction: Medline Issues Correction for Convenience Kits Containing ICU Medical Pain Management Components

Medline is correcting affected convenience kits by removing included ICU Medical pain management components containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP.

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.

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.

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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