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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Drug Recall Terminated Historical recordClass II

dilTIAZem 125mg/125mL (1 mg/mL), added to dextrose 5%, IV Bag, RX only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6054-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

dilTIAZem 125mg/125mL (1 mg/mL), added to 0.9% sodium chloride, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6055-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

vancomycin added to 0.9% Sodium Chloride, 1.25 g/250 mL (5 mg/mL), 250mL Excel Bag, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6074-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

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Drug Recall Terminated Historical recordClass II

heparin added to 0.9% sodium chloride, 2500 units/500mL (5 units/mL), IV Bag, Rx only, Cental Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-8100-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

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Drug Recall Terminated Historical recordClass II

oxyTOCIN, 40 units added to 0.9% sodium chloride 1000 mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-8069-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL, IV Bag, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-6044-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

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Drug Recall Terminated Historical recordClass II

oxyTOCIN 30 units added to Lactated Ringer's 500 mL, IV Bag, Rx only, Cental Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-6039-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

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Drug Recall Terminated Historical recordClass II

EPINEPHrine added to dextrose 5%, 4mg/250ml (16 mcg/mL), IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-7018-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

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Drug Recall Terminated Historical recordClass II

EPINEPHrine added to 0.9% sodium chloride, 4mg/250mL (16 mcg/mL), IV Bag, RX only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-8093-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

EPINEPHrine, 2 mg added to dextrose 5% 250mL, Concentration = 8 mcg/mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6030-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

PHENYLephrine added to 0.9% sodium chloride 50 mg/250mL (200mcg/mL), IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043. NDC:72196-7039-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

PHENYLephrine, added to 0.9% sodium chloride, 40mg/250ml (160mcg/mL), IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6092-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

PHENYLephrine added to 0.9% sodium chloride, 20mg/250ml (80 mcg/mL), IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-7025-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

PHENYLephrine, added to 0.9% sodium chloride, 10mg/250ml (40mcg/mL), IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6058-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

PHENYLephrine 1,000 mcg/10mL, (100mcg/mL) in 0.9% sodium chloride, 10 mL Syringe, Rx Only, CAPS, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6009-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

CARDIOPLEGIA SOLUTION, 25 mEq K, SUTTER CARDIOPLEGIA, Total Volume = 572.64 mL, IV Bag, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0217-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Neonatal TPN Starter Bag, Amino Acids (trophamine) 4%/Dextrose 10% with CALCIUM and HEPARIN, IV Bags, total volume = 250mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0422-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Neonatal TPN Starter Bag, Amino Acids (trophamine) 3.5%/Dextrose 10% with HEPARIN, IV Bag, total volume = 250mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0431-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Neonatal TPN Starter Bag, Amino Acids (trophamine) 3.5% / Dextrose 10% with low calcium and HEPARIN, IV Bag, total volume = 250mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0429-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Neonatal TPN Starter Bag, Amino Acids (trophamine) 3%/Dextrose 10% with low calcium and HEPARIN, IV Bag, total volume = 250mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0428-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recall initiated: August 17, 2023
Reported by FDA: September 6, 2023
Distribution: Nationwide in the USA

View recall →

Data last updated: November 1, 2026 ET

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.