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Recall totals

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

37,326
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,859
Class I recallsReasonable probability of serious health consequences
24,440
Class II recallsTemporary or medically reversible health consequences
2,900
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 2,095 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,440
Class I9,859
Class III2,900
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2

Showing 4,861–4,880 of 21,229 recalls

FDA Recall United States TerminatedTerminated: October 30, 2023Historical recordClass II

Rocky Mountain Pies, LLC

Product
Red Button Vintage Creamery French Silk Pie, Net Wt. 31.88 o…
Reason
Pies labeled as Red Button French Silk may contain Turtle Cream Pies containing almonds which are not declared on the French Silk label.
Published
December 28, 2022
Distribution
Multiple states

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FDA Recall TerminatedTerminated: March 15, 2024Historical recordClass III

Lacosamide Oral Solution, USP, CV, 10mg/mL, packaged in 200 mL bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured By: HETERO LABS LIMITED, Jeedimetla, Hyderabad - 500 055, India, NDC 31722-627-26

by Camber Pharmaceuticals, Inc

Reason
Failed Excipient Specifications: out of specification result observed for p-Hydroxybenzoic Acid content
Published
December 21, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 20, 2023Historical recordClass II

Menastil, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233-711-01.

by Atlantic Management Resources Ltd.

Reason
cGMP Deviations
Published
December 21, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 20, 2023Historical recordClass II

ProSirona, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Dist. by: Endometriosis Assoc. Inc. (International), Mfg. by Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233-712-01.

by Atlantic Management Resources Ltd.

Reason
cGMP Deviations
Published
December 21, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 20, 2023Historical recordClass II

Neuroquell, A Homeopathic Drug, Calendula Oil, packaged in1/8 Fl. oz. (3.5 g) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233712-01.

by Atlantic Management Resources Ltd.

Reason
cGMP Deviations
Published
December 21, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 20, 2023Historical recordClass II

Neuroquell Plus, Advanced Formula, A Homeopathic Drug, Calendula Oil packaged in 0.22 Fl. oz. (6.6 mL) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233712-01.

by Atlantic Management Resources Ltd.

Reason
cGMP Deviations
Published
December 21, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 10, 2025Historical recordClass I

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.

by Exela Pharma Sciences LLC

Reason
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration.
Published
December 21, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 10, 2025Historical recordClass I

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx only, Manufactured and Distributed by: Exela Pharma Sciences, LLC Lenoir, NC 28645. Carton NDC 51754-5001-5, vial NDC 51754-5001-1.

by Exela Pharma Sciences LLC

Reason
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration.
Published
December 21, 2022
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: May 11, 2023Historical recordClass II

St. Jean's Coast Mountain Resources Ltd. (dba) St. Jean's Ca

Product
Sardines in tomato sauce packed in cans labeled in part, "WI…
Reason
Canned sardines in tomato sauce recalled due to high levels of histamine.
Published
December 21, 2022
Distribution
Distributed wholesale to 148 retail cust…

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FDA Recall OngoingHistorical recordClass II

0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE, USP - 900 mg, WATER FOR INJECTION, USP - qs, 1000mL Bag, 12 PK, Rx Only, Fresenius Medical Care North America, Waltham, MA 02451, NDC 49230-300-10

by Fresenius Medical Care Holdings, Inc.

Reason
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Published
December 14, 2022
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: December 13, 2022Historical recordClass II

Taylor Farms Northwest, LLC

Product
Taylor Farms Carrot - Celery Sticks, Refrigerated & Ready To…
Reason
Metal fragment. A piece of metal about 3/4 inch was found in retail package.
Published
December 14, 2022
Distribution
Distributed in Washington only.

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FDA Recall United States TerminatedTerminated: December 13, 2022Historical recordClass II

Taylor Farms Northwest, LLC

Product
Taylor Farms Guacamole Tray - Large, Refrigerated & Ready To…
Reason
Metal fragment. A piece of metal about 3/4 inch was found in retail package.
Published
December 14, 2022
Distribution
Distributed in Washington only.

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FDA Recall United States TerminatedTerminated: December 13, 2022Historical recordClass II

Taylor Farms Northwest, LLC

Product
Taylor Farms Jicama Sticks, Refrigerated & Ready To Eat prod…
Reason
Metal fragment. A piece of metal about 3/4 inch was found in retail package.
Published
December 14, 2022
Distribution
Distributed in Washington only.

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FDA Recall United States TerminatedTerminated: October 24, 2023Historical recordClass II

Betty Buzz LLC

Product
Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & M…
Reason
Beverage has off-odor
Published
December 14, 2022
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Nestle-USA, Inc. (Corporate Office)

Product
Nestle Toll House Edible Chocolate Chip Cookie Dough package…
Reason
Potential of foreign material within product.
Published
December 14, 2022
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: April 6, 2023Historical recordClass I

GREEN DAY PRODUCE

Product
Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC…
Reason
Product found to be contaminated with Listeria monocytogenes
Published
December 14, 2022
Distribution
Product was distributed to 18 distributo…

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FDA Recall TerminatedTerminated: August 1, 2024Historical recordClass III

Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads, Net weight 3.7g (60 cleansing pads Net weight 3.7 g each per carton,) Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 300025, NDC 42192-113-60

by Acella Pharmaceuticals, LLC

Reason
Subpotent drug: Out of specification for assay at the end-of-shelf-life 24-month period.
Published
December 7, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 28, 2024Historical recordClass III

Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release Tablets USP, packaged as (a) 20 count carton NDC 49032-273-20; (b) 30 count carton, NDC49032-273-30; Distributed by: Walmart Inc., Bentonville, AR 72716, Product of India

by Dr. Reddy's Laboratories, Inc.

Reason
Failed dissolution specifications
Published
December 7, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: December 13, 2023Historical recordClass II

Desmopressin Acetate Tablets 0.2mg, 100-count bottles, RX Only, Distributed by: Avet Pharmaceuticals Inc. East Brunswick, NJ 08816, NDC 23155-490-01

by Heritage Pharmaceuticals Inc

Reason
Subpotent Drug
Published
December 7, 2022
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Daytrana (methylphenidate transdermal system), Delivers 15 mg over 9 hours, (1.6 mg/hr), 30 patches per box, Rx only, Manufactured for Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5553-3.

by Noven Pharmaceuticals Inc

Reason
Defective Delivery System: Recalled lot was found to be out of specification for shear. Shear is an attribute related to the adhesive properties of the transdermal patches.
Published
December 7, 2022
Distribution
Nationwide

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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.

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