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Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated November 8, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product: Fresh Thyme Original Hummus with Pretzels 4.1 oz. UPC 41330…
Reason: Product has potential to be contaminated with Listeria monocytogenes
Published: September 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product: Bucee's Texas Spicy Hummus w/ Pretzels 4.1 oz. UPC 850157003…
Reason: Product has potential to be contaminated with Listeria monocytogenes
Published: September 25, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 13, 2020Historical recordClass I

Pita Pal Foods LP

Product: Bucee's Garlic Hummus with Pretzels 4.1 oz UPC 850157000312…
Reason: Product has potential to be contaminated with Listeria monocytogenes
Published: September 25, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 4, 2020Historical recordClass I

Milk of Magnesia USP, 2400 mg/30 mL, Magnesium Hydroxide 2400 mg, 30 mL unit dose cups, For Institutional Use Only, packaged in 100-count cartons of 10 trays x 10 unit dose cups, Major Pharmaceuticals, Livonia, MI 48152, NDC 0904-6846-73.

by Plastikon Healthcare LLC

Reason: Microbial Contamination of Non-Sterile Products: product failed bioburden testing for Total Aerobic Microbial Count.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg, 500 Tablets per bottle, NDC 42291-297-50.

by AVKARE Inc.

Reason: Failed Stability Specifications.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 25, 2023Historical recordClass II

Bacteriostatic Water for Injection, USP, 30 mL vials, Rx only, Mfd. for: Hospira, Inc., Lake Forest, IL 60045 USA. NDC Vial: 0409-3977-01; NDC Carton: 0409-3977-03

by Pfizer Inc.

Reason: Lack of Assurance of Sterility
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 28, 2021Historical recordClass III

Pramipexole Dihydrochloride Tablets 0.125 mg,90-count bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Phamaceuticals Ltd. Baddi Himachal Pradesh, India. NDC 33342-031-10

by Macleods Pharma Usa Inc

Reason: Subpotent Drug: Out of specification result during stability study in Pramipexole Dihydrochloride Tablets 0.125 mg
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 16, 2020Historical recordClass III

Gatifloxacin Ophthalmic Solution 0.5%, 2.5 mL per bottle, Rx Only, Mfd. for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. Made in India. NDC: 0378-5431-35

by Mylan Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications:OOS for unknown impurity.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 9, 2020Historical recordClass III

Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC: 60687-362-11), Distributed by American Health Packaging, Columbus, OH

by American Health Packaging

Reason: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms and Strengths section of the insert that incorrectly lists the tablet description coding for the tablets.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 17, 2019Historical recordClass III

Seattle Gourmet Foods Inc.

Product: FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms…
Reason: FungusAmongUs Shiitake Organic Mushrooms are recalled due to undeclared Sulfites. the Florida Department of Agriculture and Consumer Services tested and found 0.33 mg Sulfites per serving.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 23, 2019Historical recordClass II

Tri-Union Frozen Products, Inc.

Product: Lemon Chive Chicken of the Sea Wild-Caught Pink Salmon Skinl…
Reason: Customer reported that a small percentage of pouches of Salmon to be bloated. Testing found that bloating was due to production of CO2 as a result of microbial activity of non-heat resistant non-spore forming mesophilic aerobic or facultative spoilage organisms.
Published: September 18, 2019
Distribution: West Virginia, Ohio, Pennsylvania and Ma…

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FDA Recall United States TerminatedTerminated: September 23, 2019Historical recordClass II

Tri-Union Frozen Products, Inc.

Product: Cracked Pepper Chicken of the Sea Wild-Caught Pink Salmon Sk…
Reason: Customer reported that a small percentage of pouches of Salmon to be bloated. Testing found that bloating was due to production of CO2 as a result of microbial activity of non-heat resistant non-spore forming mesophilic aerobic or facultative spoilage organisms.
Published: September 18, 2019
Distribution: West Virginia, Ohio, Pennsylvania and Ma…

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FDA Recall United States TerminatedTerminated: March 10, 2020Historical recordClass II

Natures One Inc

Product: PediaSmart Organic Soy Vanilla Beverage Mix, 12.7 oz. (360g)…
Reason: Undeclared milk allergen.
Published: September 18, 2019
Distribution: Distributed to AL, AR, AZ, CA, CO, CT, D…

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FDA Recall United States TerminatedTerminated: January 14, 2021Historical recordClass III

Jivan Shakti Inc.

Product: Plastic Bottles labeled with: "Ancient Youth Secret - Since…
Reason: Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis revealed no Vitamin D in product.
Published: September 18, 2019
Distribution: Product was distributed in: AZ, CA, CT,…

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FDA Recall United States TerminatedTerminated: March 10, 2020Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product: Trader Joes - Green Tea Item Code 64669, UPC Code 00645003.…
Reason: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 10, 2020Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product: Trader Joes - Vanilla Item Code 64500, UPC Code 00645003. Pr…
Reason: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 10, 2020Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product: Bubbies Mochi Ice Cream Strawberry, Triple Chocolate Item Co…
Reason: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 10, 2020Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product: Bubbies Mochi Ice Cream Premium Variety Pack (Strawberry, G…
Reason: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 10, 2020Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product: Bubbies Mochi Ice Cream -Vanilla Item Code CS800002, UPC Cod…
Reason: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Published: September 18, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 10, 2020Historical recordClass II

Bubbies Homemade Ice Cream and Desserts, Inc.

Product: Bubbies Mochi Ice Cream -Triple Chocolate Item Code CS800012…
Reason: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's Mochi six-piece products because of the potential for "free-floating" foreign plastic pieces in the product.
Published: September 18, 2019
Distribution: Nationwide

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Data last updated: November 8, 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.