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Recall totals

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

37,115

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 18, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

CYCLOSPORINE 2% MCT OIL SUSP, Rx only, Red Mountain Compounding Rx

by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Reason: Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Published: November 3, 2021
Distribution: 494 patients/consumers received prescrip…

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FDA Recall Terminated Historical recordClass II

CYCLOSPORIN 0.2% OIL OPTH SUSP, Rx only, Red Mountain Compounding Rx

by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Reason: Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Published: November 3, 2021
Distribution: 494 patients/consumers received prescrip…

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FDA Recall Terminated Historical recordClass II

ASCORBIC/GLUTATHIONE 1.25/1.25% OPTH SOLN, Rx only, Red Mountain Compounding Rx

by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Reason: Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Published: November 3, 2021
Distribution: 494 patients/consumers received prescrip…

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FDA Recall Terminated Historical recordClass II

ASCORBIC ACID (NON-CORN) 500MG/ML SOLN (PF), Rx only, Red Mountain Compounding Rx

by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Reason: Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Published: November 3, 2021
Distribution: 494 patients/consumers received prescrip…

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FDA Recall Terminated Historical recordClass II

ASCORBIC ACID (NON-CORN) 500MG/ML MDV SOLN, Rx only, Red Mountain Compounding Rx

by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Reason: Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Published: November 3, 2021
Distribution: 494 patients/consumers received prescrip…

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FDA Recall Terminated Historical recordClass II

LEVOCARNITINE 100MG/ML MDV SOLN, Rx only, Red Mountain Compounding Rx

by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Reason: Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Published: November 3, 2021
Distribution: 494 patients/consumers received prescrip…

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FDA Recall Terminated Historical recordClass II

Magnesium Chloride, 200 mg/mL MDV INJ, Rx only, Red Mountain Compounding Rx

by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Reason: Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Published: November 3, 2021
Distribution: 494 patients/consumers received prescrip…

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FDA Recall Terminated Historical recordClass II

Calcium Chloride, 100 mg/mL MDV INJ, Rx only, Red Mountain Compounding Rx

by First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Reason: Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Published: November 3, 2021
Distribution: 494 patients/consumers received prescrip…

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FDA Recall United States Terminated Historical recordClass I

Nestle Usa Inc

Product: Nature's Heart Pineapple Chili Cashew Glazed Mix 1.5oz poly…
Reason: Undeclared Allergen - Peanuts
Published: November 3, 2021
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Nestle Usa Inc

Product: Nature's Heart Toasted Coconut Chips 1.5oz poly film pouche…
Reason: Undeclared Allergen - Peanuts
Published: November 3, 2021
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Nestle Usa Inc

Product: Nature's Heart Mango Turmeric Cashew Glazed Mix 1.5oz poly…
Reason: Undeclared Allergen - Peanuts
Published: November 3, 2021
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Nestle Usa Inc

Product: Nature's Heart Superfood Trail Mix 1.5oz poly film pouches…
Reason: Undeclared Allergen - Peanuts
Published: November 3, 2021
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Kwokcheng Enterprise, Inc. dba Fullei Fresh

Product: All products are stored refrigerated and labeled with Fullei…
Reason: Firm is voluntarily recalling all lots/codes of bean and soy sprouts in commerce due to the potential for contamination with Listeria monocytogenes.
Published: November 3, 2021
Distribution: All bean and soy sprout consignees are w…

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FDA Recall United States Terminated Historical recordClass II

SIMPLE MILLS

Product: Almond Flour Crackers fine ground sea salt packaged in a whi…
Reason: Undeclared Milk Allergen.
Published: November 3, 2021
Distribution: Multiple states

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FDA Recall Terminated Historical recordClass II

Imipramine Pamoate Capsules 125 mg, 30-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 UNited States. Manufactured by: Lupin Limited, Pithampur, (M.P.) 454 775 India NDC# 68180-316-06

by Lupin Pharmaceuticals Inc.

Reason: Out of specification result observed in a dissolution test at the 9-month long term stability time point.
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules per bottle within a carton, Distributed by Cardinal Health, Dublin, OH 43017, NDC 70000-0232-1

by Dr. Reddy's Laboratories, Inc.

Reason: CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-136-06

by Teva Pharmaceuticals USA

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.

by Teva Pharmaceuticals USA

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC Frazer, PA 19355, Manufactured in Ireland, NDC 59310-111-06

by Teva Pharmaceuticals USA

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-530-08.

by Teva Pharmaceuticals USA

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Published: October 27, 2021
Distribution: Nationwide

View recall →

Data last updated: September 18, 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.