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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.

37,115
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
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 7,501–7,520 of 17,327 recalls

FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product
Mega Cranberry Almond Chicken Salad on Stone Ground Wheat Br…
Reason
Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published
October 23, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product
Market Sandwich Artisan Style Ranch Chicken Salad sandwich,…
Reason
Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published
October 23, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product
Market Sandwich Ranch Chicken Salad on White Bread Net Wt. 5…
Reason
Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published
October 23, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product
Speedy good to go Chicken Salad on Wheat Bread. Net Wt 4.7oz…
Reason
Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published
October 23, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

E.A. Sween Co.

Product
Chicken Salad on White Bread Sandwich, Net Wt. 5 oz. 142g),…
Reason
Various sandwiches have the potential to be contaminated with Listeria monocytogenes.
Published
October 23, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Rifampin for Injection, USP, 600 mg/vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103; NDC 67457-445-60.

by Mylan Laboratories Limited (Sterile Products Division)

Reason
Failed Impurities/Degradation Specifications: discoloration due to elevated unknown impurity results which could decrease the effectiveness of the product.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Sodium Chloride Injection USP 0.9%, packaged in 1 - 125 mL Ultraject Prefilled Syringe For Power Injection per carton, RFID Technology, Rx Only, Manufactured by: Liebel-Flarshelm Company, LLC., Raleigh, NC 27616; NDC 0019-1188-27.

by GUERBET LLC

Reason
Labeling: Not Elsewhere Classified: RFID formatting error which reads product in Ultraject syringe as expired and will not allow injection of product by the Optivantage injector.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Optiray 320 (ioversol) Injection 68%, 320 mg/mL Organically Bound Iodine, packaged in 1 - 100 mL Ultraject Prefilled Syringe For Power Injection per carton, RFID Technology, Rx Only, Manufactured by: Liebel-Flarshelm Company, LLC., Raleigh, NC 27616; NDC 0019-1323-00.

by GUERBET LLC

Reason
Labeling: Not Elsewhere Classified: RFID formatting error which reads product in Ultraject syringe as expired and will not allow injection of product by the Optivantage injector.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13

by Pfizer Inc.

Reason
Lack of Assurance of Sterility: Bag has the potential to leak.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol tablets, 0.5 mg, 100-count bottles, Rx only, Distributed by Epic Pharma, LLC Laurelton, NY 11413, NDC 42806-087-01

by Epic Pharma, LLC

Reason
Presence of Foreign Tablets/Capsules: Estradiol 1 mg was found in a 100 count bottle of Estradiol 0.5 mg Tablets.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

DrKids Himasal Natural Nasal Saline Solution, packaged in Pre-measured Singe-Use Vials a) 0.5 mL Each (20 count) UPC 37030244608; b) 1.5 mL Each (20 count) UPC 370302446098, Manufactured in USA by: UNIPHARMA, LLC Tamarac, FL 33321

by Unipharma, Llc.

Reason
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

DrKids Children's Natural Cough Syrup English Ivy Leaf, packaged in Pre-measured Single-Use Vials 0.17 fl. oz. (5 mL) Each 3.4 fl. oz. (100 mL), Manufactured in USA by: UNIPHARMA, LLC Tamarac, FL 33321 UPC 370302489026

by Unipharma, Llc.

Reason
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured By Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053. NDC 60432-212-08

by Morton Grove Pharmaceuticals, Inc.

Reason
Failed Impurities/Degradation Specifications - failed specs for Prednisolone Impurity 14
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sandoz Ranitidine Hydrochloride Capsules 300mg 30 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ 08540 Product of India NDC 0781-2865-31

by Sandoz, Inc

Reason
CGMP Deviations: Detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA).
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sandoz Ranitidine Hydrochloride Capsules 150mg 500 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ 08540 Product of India NDC 0781-2855-05

by Sandoz, Inc

Reason
CGMP Deviations: Detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA).
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sandoz Ranitidine Hydrochloride Capsules 150mg 60 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ Product of India NDC 0781-2855-60

by Sandoz, Inc

Reason
CGMP Deviations: Detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA).
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Major Infants' Gas Relief Drops, Simethicone Oral Suspension USP, 1 FL OZ (30 mL) bottle, Distributed by: Major Pharmaceuticals 17177 N Laurel Park Drive, Suite 233 Livonia, MI 48152 USA. NDC 0904-5894-30

by GCP Laboratories Inc

Reason
Microbial Contamination of Non-Sterile Product.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Abbott Calcilo XD, Low-calcium Vitamin D-Free Infant formula…
Reason
Off color and odor. Compromised can seam due to product (powder) in the seam, this poor seal potentially allowed air into the container.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenylephrine Hydrochloride Ophthalmic Solution, USP, 2.5%, 15 mL bottle, Rx only, Mfd. by: Akorn, Inc., Lake Forest, IL 60045; NDC 17478-201-15.

by Akorn, Inc.

Reason
Lack of Assurance of Sterility: Out of specification results for container closure test which cannot guarantee the sterility of the product.
Published
October 9, 2019
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Losartan Potassium/ Hydrochlorothiazide Tablets, USP 100mg/25mg, 90 tablets per bottle, Rx Only, Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920. NDC: 13668-118-90

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 9.82 parts per million.
Published
October 9, 2019
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.