Skip to main content

Data Explorer

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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 7,061–7,080 of 18,020 recalls

FDA Recall Terminated Historical recordClass II

nICARdipine HCl (0.1 mg/mL) 1 mg/10mL, in 0.9% Sodium Chloride Injection USP, 10 ml in a 20mL syringe, Rx Only, PharMEDium Services LLC 12620 W. Airport Boulevard #130 Sugar Land, TX 77470. NDC 71019-206-01

by PharMEDium Services, LLC

Reason
Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published
April 15, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate, 5 mg per mL, 50 mg per 10 mL, In 0.9% Sodium Chloride 10 mL syringe, For IV Use Preservative Free PharMEDium 913 N. Davis Ave. Cleveland, MS NDC 71030-003-12

by PharMEDium Services, LLC

Reason
Firm is recalling 46 lots of various products because of a lack of sterility assurance.
Published
April 15, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 10 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-02

by Akorn Inc

Reason
Failed impurities/degradation specification: Out-of-Specification result for total impurity at 4.1% (Limit: NMT 3.0%) during retained sample testing.
Published
April 8, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Phytonadione Injectable Emulsion, USP, 10 mg/mL 1 mL ampule (NDC 43598-405-11) packaged in 25 x 1 mL Single-Dose Ampules per carton (NDC 43598-405-16); Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540.

by Dr. Reddy's Laboratories, Inc.

Reason
Defective Container: Recall is due to breaking and shattering of ampules upon opening
Published
April 8, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, NDC 68180-982-01

by Lupin Pharmaceuticals Inc.

Reason
Presence of Foreign Tablet/ Capsule: Product complaint received indicating mix-up of one lisinopril 5mg tablet inside of a 30 mg, 100-count bottle of Lisinopril Tablets.
Published
April 8, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

New Capstone, Inc

Product
ReStructure VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G…
Reason
The firm was notified that the labeling does not include the word milk on the ingredient statement
Published
April 8, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Nystatin Oral Suspension, USP, 100,000 units per mL, Cherry/Peppermint Flavor, 16 fl oz (473 mL) bottle, Rx ONLY, pai Pharmaceutical Associates, Inc., Greenville, SC 29605; NDC 0121-0810-16.

by PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Reason
SubPotent Drug: Low out-of-specification results for assay testing.
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Tacrolimus Capsules, USP 5mg, 100-count bottle, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505, NDC 0378-2047-01

by Mylan Pharmaceuticals Inc.

Reason
Presence of foreign tablet/capsule - Potential presence of commingled one Tacrolimus 1 mg capsule in 5 mg bottles.
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Colostat, Homeopathic Remedy, 1 fl. oz. (30 mL) per bottle, 20% Ethanol, Dist. by Energique, Inc., 201 Apple Blvd., Woodbine, IA 51579, NDC 44911-0411-1

by Grato Holdings, Inc.

Reason
Labeling mix-up - Indications on product label are incorrect.
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Touchstone Essentials Organic Super Protein Vanilla Coconut…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Touchstone Essentials Super Greens Juice - Raspberry Apple;…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Pure Planet Organic Parasite Cleanse; Net Wt. 174g Glass Ja…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Springboard Green Power, Dietary Supplement; 240g Plastic B…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
RAWr! Life Organic Superfoods; Dietary Supplement; 300g Pla…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
L.O.V.E. Supermeal Vanilla Chai: 1320g Plastic Bottle, 660…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
L.O.V.E. Supermeal Original: 420g Plastic Bottle, 1396g Pla…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Purim Daily Fiber Blend - Original unflavored; 540g Plastic…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Daily Fiber Blend - Caramel Apple Flavor; Organic Plant Pow…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Nested Naturals Super Kids; Superfood Powder Full of Nutrie…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Organic By Nature, Inc.

Product
Erom, Inc. Slim Natural Raw Meal; Bulk; Finished product i…
Reason
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Published
April 1, 2020
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.