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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
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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 2,561–2,580 of 18,346 recalls

FDA Recall Ongoing Historical recordClass I

Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake FOrest, IL 60045, NDC 0409-4911-11 (carton), 0409-4911-34 (case).

by Pfizer Inc.

Reason
Presence of Particulate Matter; identified as glass
Published
January 24, 2024
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass I

8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 50 mL Syringe per Carton, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6637-24 (carton), 0409-6637-14 (case).

by Pfizer Inc.

Reason
Presence of Particulate Matter; identified as glass
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose Vials per carton, Ready to Use, For Intravenous Infusion, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-237-10

by Par Sterile Products LLC

Reason
Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Freskaro refresh & revitalize Magnesium Citrate Saline Laxative Oral Solution Cherry Flavor 10 fl. oz, Manufactured by: Pharma Lobis, 7400 Alumax Dr., Texarkana, TX 75501, NDC 82645-312-10.

by Pharma Nobis LLC

Reason
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Grape Flavor 10 fl. oz, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, NDC 51316-881-10.

by Pharma Nobis LLC

Reason
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Walgreens Dye-Free Magnesium Citrate Saline Laxative/Oral Solution, Sugar Free Low Sodium, Grape flavor 10 fl. oz, Distributed by: Walgreen Co, 200 Wilmot Rd, Deerfield, IL 60015, NDC 0363-0427-98.

by Pharma Nobis LLC

Reason
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Secret, powder fresh, (Aluminum chlorohydrate 24%), Anti-Perspirant/Deodorant, Topical spray can Net Wt., (a) 4OZ (113g), NDC 37000-134-11, UPC 0 37000 71109 4, (b) 6OZ (170g), NDC 37000-134-17, UPC 0 37000 71108 7; (c) twin pack-2 Topical spray cans, each can Net Wt. 6OZ (170g), NDC: 37000-134-01, UPC 0 37000 58690 6; Dist. by: Procter & Gamble, Cincinnati, OH 45202,

by The Procter & Gamble Company

Reason
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Old Spice, SWEAT DEFENSE ULTIMATE CAPTAIN, Aluminum Chlorohydrate 23.5%, Anti-Perspirant, Topical spray can 3.8 OZ (107 g), Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-385-10, UPC 0 37000 74947 9

by The Procter & Gamble Company

Reason
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Old Spice, SWEAT DEFENSE PURE SPORT PLUS, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical spray can, Net WT 3.8 oz (107 g) cans, Distr. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-387-10, UPC 0 37000 72974 7

by The Procter & Gamble Company

Reason
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Old Spice Pure Sport 2021 Gift Set, Contains: Old Spice Pure Sport Body Wash 18 Fl Oz (532 mL), 2-in-1 Shampoo & Conditioner 13.5 Fl Oz (400 mL), and Old Spice, SWEAT DEFENSE PURE SPORT PLUS, Dry Spray, (Aluminum Chlorohydrate 23.5%), Anti-Perspirant, Topical spray can, Net WT 3.8 oz (107 g). Dist. by: Procter & Gamble, Cincinnati, OH 45202. Gift Set NDC 69423-590-01, UPC 12044 04853 5

by The Procter & Gamble Company

Reason
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Secret OUTLAST Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Protecting Powder, Topical spray can 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-478-10, UPC 0 37000 74772 7

by The Procter & Gamble Company

Reason
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Secret, OUTLAST, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Completely Clean, Topical spray can 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-384-10, UPC 0 37000 74764 2

by The Procter & Gamble Company

Reason
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Published
January 24, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Secret, Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Lavender, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-383-10, UPC: 0 37000 72986 0

by The Procter & Gamble Company

Reason
Chemical contamination: presence of benzene
Published
January 24, 2024
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Secret, powder fresh, Aluminum chlorohydrate 24%, Anti-Perspirant/Deodorant, Topical spray can Net Wt., (a) 4OZ (113g), NDC 37000-134-11, UPC 0 37000 71109 4, (b) 6OZ (170g), NDC 37000-134-17, UPC 0 37000 71108 7; (c) twin pack-2 each can Net Wt. 6OZ (170g), NDC: 37000-134-01, UPC 0 37000 58690 6; Distr. by: Procter & Gamble, Cincinnati, OH 45202

by The Procter & Gamble Company

Reason
Chemical contamination: presence of benzene
Published
January 24, 2024
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass I

4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake Forst, IL 60045, NDC 0409-5534-24 (carton), 0409-5534-14 (case).

by Pfizer Inc.

Reason
Presence of Particulate Matter; identified as glass
Published
January 24, 2024
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Freskaro refresh & revitalize Magnesium Citrate Saline Laxative Oral Solution Grape Flavor 10 fl. oz, Manufactured by: Pharma Lobis, 7400 Alumax Dr., Texarkana, TX 75501, NDC 82645-311-10.

by Pharma Nobis LLC

Reason
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.
Published
January 24, 2024
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Good Neighbor Pharmacy, DYE FREE, SUGAR FREE Magnesium Citrate Saline Laxative, Oral Solution, Cherry Flavor 10 fl. oz, Distributed by AmerisourceBergen, 1 West First Ave, Conshochoken, PA 19428, NDC 46122-741-38

by Pharma Nobis LLC

Reason
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.
Published
January 24, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Mead Johnson & Company LLC

Product
Enfamil Nutramigen Hypoallergenic Infant Formula Powder with…
Reason
Product has the potential to be contaminated with Cronobacter sakazakii.
Published
January 24, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Ministry of Snacks Sweet and Savory Collection #8700
Reason
Potential Salmonella contamination of Quaker Oats Chewy Granola Bars packed in gift baskets.
Published
January 24, 2024
Distribution
U.S. distribution to the following: AK,…

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FDA Recall Completed Historical recordClass II

Tizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-180-15

by Dr. Reddy's Laboratories, Inc.

Reason
Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.
Published
January 17, 2024
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.