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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.

37,116
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potatoPublished September 16, 2026
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 8,121–8,140 of 19,198 recalls

FDA Recall Terminated Historical recordClass III

SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant, Net Wt. 2.6 oz (73g) NDC# 41595-5509-2 UPC 8 83484 71717 2 Made in Canada and Distributed by Idelle Labs, Ltd., El Paso, TX 79912

by Idelle Labs

Reason
Labeling Product Contains Undeclared API: Active Ingredient on label is not the active ingredient in the product.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP and ferrous fumarate tablets 75mg), Rx Only, Distributed by: Lupin Pharmaceuticals Inc Baltimore, MD 21202, Manufactured for: Lupin Limited Pithampur 454775 INDIA 240875, NDC 68180-866-11

by Lupin Pharmaceuticals Inc.

Reason
Failed Tablet/Capsule Specifications: Complaints related to crumbling of tablets when popped out of the blister pack.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass II

TFI Holding dba Grey Ghost Bakery

Product
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.…
Reason
The product contains undeclared sulfites.
Published
January 15, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Reichel Foods Inc.

Product
Pro2Snax To The Max snack tray containing Sweet Gala Apples,…
Reason
Products are being recalled due to Listeria monocytogenes contamination.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Reichel Foods Inc.

Product
Pro2Snax To The Max snack tray containing Sliced Apples, Har…
Reason
Products are being recalled due to Listeria monocytogenes contamination.
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wayfare Health Foods LLC

Product
Plant Based WayFare Butterscotch Pudding Organic Dairy Free,…
Reason
Product is recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wayfare Health Foods LLC

Product
Plant Based WayFare Vanilla Pudding Organic Dairy Free, Item…
Reason
Product recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published
January 15, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wayfare Health Foods LLC

Product
Plant Based WayFare Chocolate Pudding Organic Dairy Free, It…
Reason
Product recalled due to consumer complaints for bloating of package, off flavors (sourness, tart), and textural issues (grittiness, lumpiness).
Published
January 15, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

MYORISAN (isotretinoin capsules, USP), 20mg, packaged in 30-count Capsules (3 x 10 Prescription Packs) per box, Rx only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forset, IL 60045; NDC 61748-302-13.

by Akorn, Inc.

Reason
Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan 20 mg Capsules, USP erroneously contained one 10-count blister card of the 40 mg product in addition to two 10-count blister cards of the 20 mg product.
Published
January 8, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Bimatoprost Ophthalmic Solution, 0.03%, For Use in the Eyes Only, Sterile, Rx Only, 7.5 mL bottle, Manufactured by: Lupin Limited, Pithampur (M.P.), INDIA, NDC: 68180-429-03.

by Lupin Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications: Out-of-specification result observed in any other individual impurity.
Published
January 8, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Silver Bullet, Get Bigger and Harder, Works in Minutes, Lasts for Days, 10 male enhancement capsules in blister foil package, 725mg per capsule, Distributed by Silver Bullet Ltd, Golden Springs, CO, USA, UPC: 610877392698.

by Natures Rx

Reason
Marketed Without an Approved NDA/ANDA; Product contains undeclared active ingredient - Sildenafil.
Published
January 8, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ranitidine Syrup (Ranitidine Oral Solution USP), 15 mg/mL, 150 mg/10 mL per cup, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio. (a) Case of 50 cups (NDC 60687-260-69) (b) Case of 40 cups (NDC 60687-260-23 (c) Unit Dose Cup (NDC 60687-260-69)

by American Health Packaging

Reason
CGMP Deviations: Presence of NDMA impurity detected in product.
Published
January 8, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

CHICKEN OF THE SEA

Product
Chicken of the Sea Sardines in Water; Net Wt. 3.75 oz. (106…
Reason
It was discovered that one batch of sardines were incorrectly labeled - Sardines in Water instead of Sardines in Tomato sauce.
Published
January 8, 2020
Distribution
OR, CA, WA, NV, UT, CO, AZ, ID, TN.

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FDA Recall Terminated Historical recordClass II

Estriol [(16a, 17B)-Estra-1,3,5(10)-triene-3,16,17-triol; Oestriol] Micronized, USP, CAS 50-27-1, packaged in a) 1 G glass bottles, b) 5 G glass bottles, c) 25 G glass bottles, d) 100 G glass bottles, e) 500 G glass bottles, and f) 1 KG plastic bottles, Rx Only, Spectrum Chemical Mfg Corp., Gardena, CA 90248.

by Spectrum Laboratory Products

Reason
Subpotent Drug: Supplier indicated assay results did not meet specifications.
Published
January 1, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 254.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.

by PharMEDium Services, LLC

Reason
Subpotent Drug
Published
January 1, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.

by PharMEDium Services, LLC

Reason
Subpotent Drug
Published
January 1, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.

by PharMEDium Services, LLC

Reason
Subpotent Drug
Published
January 1, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ardent Mills LLC

Product
Wild Harvest Organic Unbleached All Purpose Flour, Net Wt 5…
Reason
Wild Harvest Organic Unbleached All Purpose Flour in 5 lb. bags has the potential to be contaminated with E. coli (STEC).
Published
January 1, 2020
Distribution
900 cases were distributed to 4 differen…

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FDA Recall Terminated Historical recordClass II

Gabapentin Capsules, USP 100 mg, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810, NDC 65682-198-99

by AuroMedics Pharma LLC

Reason
Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was found in Gabapentin 1000 count bottles..
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Levetiracetam Oral Solution 100mg/mL, 473 mL (16 fl. oz.) Bottles, Rx Only, Distributed by: Lannett Company, Inc. Philadelphia, PA 19136, NDC 54838-0548-80

by Lannett Company, Inc.

Reason
Microbial Contamination of Non-sterile Products: Out-of-specification results obtained for Total Aerobic Microbial Count.
Published
December 25, 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.