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Recall totals

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

37,118

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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

State: WI ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 20, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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

Five Star Gourmet Foods of Florida

Product: Simply Fresh brand MiniMeals2Go Avocado Toast (6.75 OZ) read…
Reason: Products have potential to be contaminated with Listeria monocytogenes.
Published: January 15, 2020
Distribution: Illinois, Indiana, Kentucky, Michigan, O…

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FDA Recall United States Terminated Historical recordClass I

Five Star Gourmet Foods of Florida

Product: Simply Fresh brand MiniMeals2Go Protein Pack (8.25 OZ) ready…
Reason: Products have potential to be contaminated with Listeria monocytogenes.
Published: January 15, 2020
Distribution: Illinois, Indiana, Kentucky, Michigan, O…

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FDA Recall United States Terminated Historical recordClass II

Bay State Milling Co.

Product: SimplySafe Sesame Seed Hulled; 49lbs bag; Lot #PBAT10025110
Reason: Product may be contaminated with Salmonella.
Published: January 15, 2020
Distribution: Multiple states

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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

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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

SARA LEE FROZEN FOODS

Product: Chef Pierre 37 Ounce Pumpkin Spice Latte Pie, in foil pie pa…
Reason: undeclared FD & C Red 40
Published: January 8, 2020
Distribution: Multiple states

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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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Data last updated: September 20, 2026 ET

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.