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Recall totals

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

37,063

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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026

Most affected stateHawaii 200 recalls mention this state

State: AS ×
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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

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

HYDROmorphone in Dextrose 5%, 0.5 mg/5 mL (0.1 mg/mL), 5 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2013-1

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

fentaNYL in 0.9% sodium chloride, 500 mcg/50 mL, (10 mcg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2071-3

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

fentaNYL in 0.9% sodium chloride, 100 mcg/10 mL, (10 mcg/mL), 10 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2071-2

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

fentaNYL, 2500 mcg/50 mL, (50 mcg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-3

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

fentaNYL, 250 mcg/5 mL, (50 mcg/mL), 5 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-2

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

fentaNYL, 100 mcg/2 mL, (50 mcg/mL), 3 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-1

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

HYDROmorphone in 0.9% sodium chloride, 6 mg/30 mL, (0.2 mg/mL), 30 mL Syringe, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2010-1

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

CARDIOPLEGIA SOLUTION, 36 mEq K, Maintenance 8:1, low Potassium / low dextrose, IV Bag, total volume = 500 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0108-1

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

CARDIOPLEGIA SOLUTION, low K, Maintenance 4:1 Plasmalyte/Tromethamine, Low Potassium, IV Bag, total volume = 1000 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0112-1

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, low K, Maintenance 4:1 Plasmalyte, Low Potassium, IV Bag, total volume = 1047 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0211-1

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

CARDIOPLEGIA SOLUTION, 12 mEq K, Maintenance 4:1 in Ringer's Low Potassium, IV Bag, total volume = 504.8 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0205-1

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

CARDIOPLEGIA SOLUTION, 70 mEq K, Induction 8:1, non-enriched, High Potassium, IV Bag, Total Volume = 300 mL, RX only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0214-1

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

CARDIOPLEGIA SOLUTION, 70 mEq K, Modified St. Thomas Formula low potassium, IV Bag, Total Volume = 1000 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0210-1

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

CARDIOPLEGIA SOLUTION, 106 mEq K, Modified St. Thomas Solution High Potassium High Sodium Bicarbonate, IV Bag, Total Volume = 1000 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0204-1

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

CARDIOPLEGIA SOLUTION, 60 mEq K, Induction 4:1, High Potassium, IV Bag, total volume = 830 mL, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0100-1

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

CARDIOPLEGIA SOLUTION, HIGH K, Induction 4:1, Plasmalyte/Tromethamine, High Potassium, IV Bags, total volume = 500 mL, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0111-1

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

TRANSPLANT SOLUTION, Plasma-Lyte A - 75 ml, MSA/MSG 0.92 Molar -60 ml, dextrose 70% 21.3 ml; IV Bag, Total Volume = 165 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0014-2

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

View recall →

FDA Recall Terminated Historical recordClass II

CARDIOPLEGIA SOLUTION, 7.5 mEq K, Reperfusate 4:1, low potassium, IV Bag, total volume = 238.75 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0007-1

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

CARDIOPLEGIA SOLUTION, 25 mEq K, SUTTER CARDIOPLEGIA, IV Bag, Total Volume = 572.64 mL, 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. Validation data for decontamination cycles is lacking.
Published: August 9, 2023
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

CARDIOPLEGIA SOLUTION, 15 mEq K, Reperfusate 4:1, low potassium/low tromethamine, total volume = 500mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0009-1

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 →

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.