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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.

37,113
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 5,821–5,840 of 17,229 recalls

FDA Recall Terminated Historical recordClass I

BD ChloraPrep Hi-Lite Orange 26 mL Applicator (2% w/v chlorhexidine gluconate (CHG) and 70% v/v Isopropyl alcohol (IPA)) Sterile Solution, CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co, NDC 54365-400-38

by CareFusion 213, LLC

Reason
Defective Delivery System: An increase in complaints identified endcap being loose or falling off upon activation releasing glass shards containing the solution.
Published
May 19, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Metformin HCl Extended-Release Tablets, USP, 500 mg, packaged in 500-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-142-02.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Presence of foreign substance: identified as activated carbon.
Published
May 19, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

NATURE'S SUNSHINE PRODUCTS

Product
Love & Peas Protein Rich Meal Replacement, Sugar Free, 1 LB…
Reason
The firm was notified by an ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that are marketed and sold as vegan and dairy-free.
Published
May 19, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

NATURE'S SUNSHINE PRODUCTS

Product
Love & Peas Protein Rich Meal Replacement, 1 LB 8 OZ (675 G)…
Reason
The firm was notified by its ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that are marketed and sold as vegan and dairy-free.
Published
May 19, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Imperial Platinum 2000, 1 capsule, UPC 718122040702

by QMart

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Burro en Primavera, 2 capsules, UPC 638632431055

by QMart

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

PremierZen Extreme 3000, Male Sexual Performance Enhancement, 1 Capsule, UPC 728175421887

by QMart

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

IMPERIAL GOLD 2000, Male Sexual Performance Enhancement, 1 Capsule, UPC 718122040702

by QMart

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Thumbs Up 7 Red 70K, 10 count blister pack cartons, Distributed by Ummzy LLC., Made in USA, UPC 6 17135 89467 3.

by Antoto-K

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of sildenafil and tadalafil.
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Acetaminophen, Extra Strength, Aspirin Free, 500 MG Tablets, 100-count bottles, Mfr: Major Pharmaceuticals, Livonia, MI 48152; Packaged Exclusively By: A-S Medication Solutions LLC, Libertyville, IL 60048, Product # 6967-0; NDC: 50090-5350-0; contained within Health Essentials Kit, Kit Contains: 1 bottle hand sanitzer, 1 reusable face mask, 1 bottle Acetaminophen 500 mg, 1 bag cough drops, 1 digital thermometer, 50 disposable gloves.

by A-S Medication Solutions LLC.

Reason
Labeling: Label Mix-up; The bottle of over-the-counter Acetaminophen 500mg Extra Strength, 100 count, included in Health Essential Kits, labeled incorrectly with a prescription drug label instead of an OTC drug label.
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Creative Foods Inc

Product
Bueno Coffee Substitute Creamy Hazelnut, Gluten-Free, net wt…
Reason
Bueno Coffee Substitute Creamy Hazelnut product contains undeclared hazelnut and peanut.
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Creative Foods Inc

Product
Bueno Coffee Substitute Pecan Praline, Gluten-Free, net wt.…
Reason
Bueno Coffee Substitute Pecan Praline Gluten-Free product contains undeclared peanut and barley (which contains gluten).
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Forest Mushroom Food Inc.

Product
Guan's Enoki Mushroom - Champigons d'enoki; Net Wt./ Poids…
Reason
Michigan Department of Agriculture and Rural Development sampled Enoki mushrooms and found some samples to be positive for Listeria monocytogenes.
Published
May 12, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Evrysdi (risdiplam) for oral solution, 60 mg/80mL (0.75mg/mL), 80 mL total volume after constitution, Rx only, Distributed by: Genentech, Inc. NDC:50242-175-05

by Genentech Inc

Reason
Defective Container: complaints received regarding some incorrect press-in-bottle-adapters (PIBA), the incorrect PIBAs have a female instead of male fit so they cannot be used in combination with co-packed syringes.
Published
May 5, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxygen, Compressed, USP UN 1072, packaged in cylinders labeled as: a) M6 Medical Gas Cylinder, b) C Medical Gas Cylinder; c) D Medical Gas Cylinder; d) E Medical Gas Cylinder; e) M Medical Gas Cylinder; f) H Medical Gas Cylinder, Rx only, Grace Healthcare 1418 31st Avenue Gulfport, MS 39501 228-863-3331

by Grace Healthcare Medical, Inc

Reason
cGMP deviations
Published
May 5, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW LIFE Distributors Los Angeles CA 90005 UPC 7 15122 05089 4

by Na Na Collection

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Published
May 5, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

PremierZen Platinum 5000, Packaged in paper packaging with a pill blister, 1 capsule per box, Distributed by New Premier Group Los Angeles CA 90006

by Na Na Collection

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.
Published
May 5, 2021
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Imperial Extreme 2000 Capsules, 2000 mg, 1 count blister cards, distributed S&B Shopper LLC. Little Ferry, NJ UPC 7 18122 04073 5

by S & B Story LLC

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and sildenafil.
Published
May 5, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PremierZen Black 5000 capsules, 1 capsule per card/24 capsules per box, Distributed by New Premier Group Los Angeles CA 90006 UPC 7 2817542189 4

by Namoo Enterprise LLC

Reason
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and sildenafil.
Published
May 5, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Non-Sterile Solution - Hi-Lite Orange, 0.10 fl. oz. (3 ml) each, 25 applicators in carton, applicator is sterile if package is intact. CareFusion El Paso, TX 79912, NDC 054365-400-11 Cat. No. 260415

by CareFusion 213, LLC

Reason
CGMP Deviations: Product is being recalled because at labeled storage conditions of 30*C/75% Relative Humidity, there is the potential for growth of Aspergillus penicillioides, a type of fungus, resulting in a breach of the package integrity.
Published
May 5, 2021
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.