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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,113
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 5,161–5,180 of 21,178 recalls

FDA Recall Ongoing Historical recordClass II

Betaxolol Ophthalmic Solution, USP 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-705-10

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Artificial Tears Solution, Lubricant Eye Drops, Polyvinyl Alcohol 1.4%, 15 mL (0.5 fl. oz.) per bottle, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-060-12

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Artificial Tears OINTMENT, Lubricant Eye Ointment, Net Wt. 3.5 g (1/8 oz.) per tube, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-062-35

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

AK-POLY-BAC brand of Bacitracin cand Polymixin B Sulfate Ophthalmic Ointment USP, 3.5 g (1/8 oz.) tube, Rx only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-238-35

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Daptomycin for Injection 350 mg/vial 1 Single-dose vial, Rx only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703 Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213, India. NDC 16729-0434-05

by ACCORD HEALTHCARE, INC.

Reason
Labeling mixup: cartons labeled as Daptomycin 350 mg/vial were found to contain vials of Daptomycin 500 mg per vial
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection, USP) with Epinephrine 1:200,000 (as bitartrate), 0.25%, 25 mg per 10 mL (2.5 mg per mL), 10 mL Single Dose Vial (NDC 63323-468-01), packaged in 25 Single Dose Vials per tray (NDC 63323-468-17), Rx only, Fresenius Kabi, Lake Zurich, IL 60047.

by Fresenius Kabi USA, LLC

Reason
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sensorcaine (Bupivacaine HCl and Epinephrine Injection, USP) with Epinephrine 1:200,000 (as bitartrate), 0.5%, 250 mg per 50 mL (5 mg per mL), 50 mL Multiple Dose Vial (NDC 63323-463-01), packaged in 25 Multiple Dose Vials per tray (NDC 63323-463-57), Rx only, Fresenius Kabi, Lake Zurich, IL 60047.

by Fresenius Kabi USA, LLC

Reason
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sensorcaine (Bupivacaine HCl and Epinephrine Injection, USP) with Epinephrine 1:200,000 (as bitartrate), 0.25%, 125 mg per 50 mL (2.5 mg per mL), 50 mL Multiple Dose Vial (NDC 63323-461-01), packaged in 25 Multiple Dose Vials per tray (NDC 63323-461-57), Rx only, Fresenius Kabi, Lake Zurich, IL 60047.

by Fresenius Kabi USA, LLC

Reason
Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 15 FRZN DOUGH 6 oz.; G…
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 61 Dad's 8 oz.; Greco…
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 92 House of 1000 10 oz…
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 65 Garlic Knots 180/CS
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 28 Stefano 12 oz.; Gre…
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 333 PUB DOUGH 9 oz.; G…
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 12 Vic's Pizza 10 oz.;…
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 79 North Park Lounge 1…
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Sysco Merchandising and Supply

Product
Greco and Sons Dough Room Product No. 9009 Teresa's 9 oz.; G…
Reason
The dough ball products contain the undeclared allergen milk.
Published
January 25, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

ByHeart, INC.

Product
By Heart Whole Nutrition Infant Formula, Net Wt. 24 oz. 680…
Reason
Infant formula potentially contaminated with Cronobacter sakazakii
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Something South African LLC

Product
Pepper Collection 8 Tube Gift Set - a colorful assortment of…
Reason
Due to presence of mold (Aspergillus brasiliensis) and Ochratoxin A.
Published
January 25, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

TriMix Injection (PGE1/Papaverine HCl/Phentolamine Mesylate) 10mcg/20mg/1mg/mL INJECTABLE, packaged in 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.

by Northern VA Compounders PLLC

Reason
Lack of Assurance of Sterility
Published
January 18, 2023
Distribution
Nationwide

View recall →

Data last updated:

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.