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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

State: RI ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 11, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

PHENYLephrine 1,000 mcg/10mL, (100mcg/mL) in 0.9% sodium chloride, 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

PHENYLephrine 20mg/250ml added to 0.9% sodium chloride, 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

PHENYLephrine, 10mg/250ml added to 0.9% sodium chloride, 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

EPINEPHrine 8mg/250ml added to dextrose 5%, 32 mcg/mL, IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-7019-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

EPINEPHrine added to dextrose 5%, 4mg/250ml, 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cardioplegia Solution del Nido Formula, IV Bag, Total Volume = 1,052.8 mL, FOR INTRACARDIAC PERFUSION USE ONLY, PLASMA-LYTE A 1000 mL, Mannitol 20% 16.3 mL, Sodium Bicarbonate 8.4% 13 mL, Potassium Chloride 2 mEq/mL 13 mL, Magnesium Sulfate 4.06 mEq/mL 4 mL, Lidocaine 2% 6.5 mL, Approx. Osmolarity 386 mOsm/L, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-0202-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

vancomycin 1.25 g/250 mL added to 0.9% Sodium Chloride, 5 mg/mL, IV 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

EPINEPHrine 4mg/250mL added to 0.9% sodium chloride, 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

glycopyrrolate 1 mg/5 mL (0.2 mg/mL), For Anesthesia Use, Syringe, RX ONLY, CAPS, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-6084-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

vancomycin 1.25 g/250 mL added to dextrose 5%, 5 mg/mL, IV Bag, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix AZ 85043, NDC: 72196-6073-1

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue Pheonix, AZ, NDC 72196-6011-2.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

rocuronium50 mg/5 mL (10 mg/mL), Syringes Rx only, this drug was repackaged by CAPS Inc, 2200 South 43rd Avenue, Pheonix, AZ, NDC 72196-6010-1.

by Central Admixture Pharmacy Services, Inc.

Reason: Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Tydemy (drospirenone, ethinyl estradiol and levomefolate calcium tablets, 3 mg/0.03 mg/0.451 mg and levomefolate calcium tablets 0.451 mg), packaged in 1 blister of 28 tablets each (NDC 68180-904-71) further packaged in a carton of 3 blisters (NDC 68180-904-73), Distributed by: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, Manufactured by Lupin Limited, Pithampur (M.P.), INDIA

by Lupin Pharmaceuticals Inc.

Reason: Failed Stability Specification and Failed Impurities/Degradation Specifications: out of specification for inactive content ascorbic acid and MTHFRC-7impurity test
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

morphine in 0.9% Sodium Chloride, 50 mg/50 mL (1mg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C San Diego, CA 92126, NDC: 71286-2040-4

by Central Admixture Pharmacy Services Inc

Reason: Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL in 0.9% sodium chloride, 10 mcg/1 mL, (10 mcg/mL), 3 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C San Diego, CA 92126, NDC: 71286-2071-1

by Central Admixture Pharmacy Services Inc

Reason: Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published: August 9, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine in 0.9 sodium chloride, 800 mcg /10 mL, (80 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-6008-1

by Central Admixture Pharmacy Services Inc

Reason: Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published: August 9, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

midazolam in dextrose 5%, 50 mg /50 mL, (1 mg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-4036-1

by Central Admixture Pharmacy Services Inc

Reason: Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published: August 9, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

lidocaine 2%, 100 mg /5 mL, (20 mg/mL), 5 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6006-1

by Central Admixture Pharmacy Services Inc

Reason: Lack of assurance of sterility: Lack of validation data for sanitization cycles
Published: August 9, 2023
Distribution: Nationwide

View recall →

Data last updated: September 11, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.