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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.

37,118
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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 10,401–10,420 of 17,327 recalls

FDA Recall United States Terminated Historical recordClass II

The Harvard Drug Group

Product
Rugby Polyvitamin Liquid, 1 2/3 oz (50 mL)
Reason
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published
September 20, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Harvard Drug Group

Product
Rugby Ferrous Sulfate Liquid One Pint, (473 mL)
Reason
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published
September 20, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Harvard Drug Group

Product
Rugby Liquid Vitamin C Supplement, 4 oz., 118 mL
Reason
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published
September 20, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Harvard Drug Group

Product
Rugby Fer-iron Liquid, 1 and 2/3 oz., 50 mL
Reason
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published
September 20, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Harvard Drug Group

Product
Rugby D 3 Vitamin Liquid, 400 IUI/1 mL, 1 and 2/3 oz., 50 m…
Reason
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published
September 20, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

The Harvard Drug Group

Product
Rugby Cerovite Liquid, 8 oz. 236ML
Reason
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published
September 20, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

The Harvard Drug Group

Product
Rugby Calcionate Syrup, One Pint (473 mL)
Reason
The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published
September 20, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic Drops, Sterile 5ml Bottle, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA

by ImprimisRx CA, Inc., dba ImprimisRx

Reason
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Published
September 13, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Timolol-Latanoprost PF Solution (0.5-0.005)%, Ophthalmic Drops, Sterile 5ml Bottle, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA

by ImprimisRx CA, Inc., dba ImprimisRx

Reason
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Published
September 13, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Latanoprost PF Solution, 0.005%, Ophthalmic Drops in Sterile 5ml Bottles, Compounded for a licensed professional or patient use, imprimisRx, Irvine, CA

by ImprimisRx CA, Inc., dba ImprimisRx

Reason
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Published
September 13, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Curcumin Emulsion 10mg/ml Injection, Sterile 10 mL Multiple Dose Vial, For Slow IV Administration, Compounded for a licensed professional or patient use by ImprimisRx, Irvine, CA

by ImprimisRx CA, Inc., dba ImprimisRx

Reason
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Published
September 13, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Famotidine for Oral Suspension USP, 40 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Goa 403 722 INDIA, NDC 68180-150-01

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations
Published
September 13, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Madhava Honey Ltd

Product
Madhava Naturally Sweet Deliciously Organic MMM... Chocolate…
Reason
Madhava Natural Sweeteners is recalling MMM... Chocolate Chip Cookie Mix because it may contain undeclared milk.
Published
September 13, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Morphine Sulfate Oral Solution, 100 mg/ 5 mL (20 mg/mL), packaged in a 1 oz. bottle containing 30 mL with an oral syringe, Rx Only, Manufactured by: Tris Pharma, Inc. Monmouth Junction, NJ 08852, NDC 27808-082-01

by Tris Pharma Inc.

Reason
Defective container: Oral solution leaking from container.
Published
September 6, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted) bottle, Rx Only, Manufactured By: Cipla Ltd. at Medispray Laboratories Pvt. Ltd., Kundaim Goa, India; Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054, NDC 60432-065-00.

by Morton Grove Pharmaceuticals, Inc.

Reason
Presence of Foreign Substance: customer complaint of blue foreign material identified as a portion of a nitrile glove was discovered in product.
Published
September 6, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product
Amrita Pineapple Chia Energy Bar, 50gm UPC: 853009004025
Reason
Product may be contaminated with Listeria monocytogenes
Published
September 6, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product
Amrita Apricot Strawberry Protein Bar, 50gm UPC :853009004…
Reason
Product may be contaminated with Listeria monocytogenes
Published
September 6, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product
Amrita Chocolate Chip Coconut 15g Protein Bar, 60gm UPC: 85…
Reason
Product may be contaminated with Listeria monocytogenes
Published
September 6, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product
Amrita Sunflower Butter & Jelly 15g Protein Bar, 60gm UPC:…
Reason
Product may be contaminated with Listeria monocytogenes
Published
September 6, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Amrita Health Foods

Product
Amrita Dark Chocolate Quinoa 15g Protein Bar, 60gm UPC: 853…
Reason
Product may be contaminated with Listeria monocytogenes
Published
September 6, 2017
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.