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Cardinal Health 200, LLC

Cardinal Health 200, LLC Recalls

All product recalls associated with Cardinal Health 200, LLC.

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Recall Summary

Total Recalls

492

Past Year

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–20 of 492 recalls

ChemoPlus gowns: Product Code Product Description CT5500T... (Cardinal Health 200, LLC) – mislabeling (2025)

Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.

FDANov 12, 2025Nationwide• Cardinal Health 200, LLC

Salem Sump PVC Tubes (Cardinal Health) – Valve Breakage Risk (2025)

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

FDASep 18, 2025Nationwide• Cardinal Health 200, LLC

Enoxaparin Sodium Injection (Cardinal Health) - Product Mispack (2025)

Correct Labeled Product Mispack: Bags labeled for Enoxaparin Sodium Injection, 80 mg/0.8 mL, contained Enoxaparin Sodium Injection, 30 mg/0.3 mL

Class II

12 3...25

Page 1 of 25Next

Moderate

FDAAug 5, 2025KS• Cardinal Health Inc.

RECOMBINATE Antihemophilic Factor (Cardinal Health) – Temperature Deviation (2025)

CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.

Class IIModerate

FDAJul 30, 2025Nationwide• Cardinal Health Inc.

Xolair Omalizumab Injection (Cardinal Health) – Temperature Deviation (2025)

CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.

Class IIModerate

FDAJul 30, 2025Nationwide• Cardinal Health Inc.

Xolair Injection (Cardinal Health) - Temperature Exposure (2025)

CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.

Class IIModerate

FDAJul 30, 2025Nationwide• Cardinal Health Inc.

Kendall SCD Blended Comfort Sleeve (Cardinal Health) – Software Pressure Error (2025)

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

FDAMay 13, 2025AK, CA, FL +2 more• Cardinal Health 200, LLC

Kendall SCD Comfort Sleeve (Cardinal Health) – Software Pressure Error (2025)

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

FDAMay 13, 2025AK, CA, FL +2 more• Cardinal Health 200, LLC

SCD Comfort Sleeve (Cardinal Health) – Software Pressure Error (2025)

Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.

FDAMay 13, 2025AK, CA, FL +2 more• Cardinal Health 200, LLC