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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

diphenhydrAMINE 50 mg added to 0.9% sodium chloride 50 mL in 100 mL Partial Additive Bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7090-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

diphenhydrAMINE 25 mg added to 0.9% sodium chloride 50 mL in 100 mL Partial Additive Bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7089-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

vancomycin added to 0.9% sodium chloride, 1.75 g/500 mL* (3.5 mg/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7060-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

phenylephrine 50 mg added to 0.9% sodium chloride 250 mL, 200 mcg/mL, 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7039-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

NORepinephrine added to 0.9% sodium chloride, 16 mg/250 mL* (64 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7036-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

PHENYLephrine added to 0.9% sodium chloride, 20 mg/250 mL* (80 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7025-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

heparin added to 0.9% sodium chloride, 5,000 units/500 mL* (10 units/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7023-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

heparin added to 0.9% sodium chloride, 4,000 units/1,000 mL* (4 units/mL), 1,000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7022-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

EPINEPHrine added to dextrose 5%, 8 mg/250 mL* (32 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7019-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

EPINEPHrine added to dextrose 5%, 4 mg/250 mL* (16 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7018-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

potassium phosphate 30 mmole added to 0.9% sodium chloride 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7016-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

PHENYLephrine added to 0.9% sodium chloride, 25 mg/250 mL* (100 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7011-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

heparin added to 0.9% sodium chloride, 7,500 units/1,000 mL* (7.5 units/mL), 1000 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-7009-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

vancomycin added to 0.9% sodium chloride, 1.5 g/500 mL* (3 mg/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6176-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6092-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

vancomycin added to 0.9% sodium chloride, 2 g/500 mL* (4 mg/mL), 500 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6078-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

vancomycin added to 0.9% sodium chloride, 1.5 g/250 mL* (6 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6076-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

vancomycin added to dextrose 5%, 1.5 g/250 mL* (6 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6075-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 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), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6074-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

vancomycin added to dextrose 5%, 1.25 g/250 mL* (5 mg/mL), 250 mL per bag, Rx only, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, NDC 71285-6073-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Recall initiated: April 28, 2023
Reported by FDA: May 31, 2023
Distribution: Nationwide in the USA.

View recall →

Data last updated: November 2, 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.