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Central Admixture Pharmacy Services, Inc.

Central Admixture Pharmacy Services, Inc. Recalls

All product recalls associated with Central Admixture Pharmacy Services, Inc..

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Recall Summary

Total Recalls

1000

Past Year

891

Class I (Serious)

124

Most Recent

Jan 2026

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 3001–3020 of 17593 recalls

Neonatal PN Starter Bag (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

dilTIAZem Dextrose Injection (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Cardioplegia Solution (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

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Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Heparin Sodium Chloride (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Phenylephrine Sodium Chloride (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Potassium Acetate Injection (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Tromethamine Injection (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Cardioplegia Solution (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Oxytocin Sodium Chloride (Central Admixture) – Sterility Concern (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Cardioplegia Warm Induction Solution (Central Admixture) – Sterility Concerns (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

Norepinephrine Dextrose Injection (Central Admixture) – sterility risk (2023)

Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.

Class IIModerate

FDAApr 28, 2023Nationwide• Central Admixture Pharmacy Services, Inc.

MRI Biomet Pin Guide (Materialise) – Wrong Guide (2023)

The wrong tibia guide was included intended for a different patient case.

FDAApr 26, 2023Nationwide• Materialise N.V. Technologielaan 15 Heverlee Belgium

HeartSine Defibrillator (HeartSine) – Battery Failure (2023)

Single use battery and electrode cartridge may be rendered inoperable due to depleted battery cells which could prevent the defibrillator from analyzing patient condition or delivering therapy correctly.

FDAApr 26, 2023Nationwide• HeartSine Technologies Ltd 207 Airport Road West Belfast United Kingdom

Culinaria Cashew & Macadamia Mix (Schutzman Company) – Label Error (2023)

Label mix-up.

Class IIModerate

FDAApr 26, 2023IL, IN, MO• A. L. Schutzman Company, Inc.

Aspira Pleural Drainage Catheter Tray (Merit Medical) - Valve Malfunction (2023)

There is a potential that valve assemblies will not open. preventing fluid from draining.

FDAApr 22, 2023Nationwide• Merit Medical Systems, Inc.

Aspira Drainage Catheter Tray (Merit Medical) - Valve Malfunction (2023)

There is a potential that valve assemblies will not open. preventing fluid from draining.

FDAApr 22, 2023Nationwide• Merit Medical Systems, Inc.

Aspira Valve Repair Kit (Merit Medical) - Valve Malfunction (2023)

There is a potential that valve assemblies will not open. preventing fluid from draining.

FDAApr 22, 2023Nationwide• Merit Medical Systems, Inc.

Aspira Peritoneal Drainage Catheter Tray (Merit Medical) - Valve Malfunction (2023)

There is a potential that valve assemblies will not open. preventing fluid from draining.

FDAApr 22, 2023Nationwide• Merit Medical Systems, Inc.

Coachmen Nova (Coachmen) - Fuel System Issue (2023)

Forest River, Inc. (Forest River) is recalling certain 2021-2023 Coachmen Galleria, Beyond, Forester, Sunseeker, and 2021-2024 Nova motorhomes, equipped with certain Cummins Onan QG 2800i, and Onan QG 2800i EVAP generator sets. The fuel hose between the inline fuel filter and the Injection Pump Module (IPM) may have inadequate clamp force, possibly resulting in a gasoline leak.

NHTSAApr 21, 2023Nationwide• COACHMEN

Ground Cumin (Lipari Foods) – Salmonella Contamination (2023)

Product tested positive for Salmonella

FDAApr 20, 2023AL, AR, FL +13 more• Lipari Foods Operating Company, LLC.