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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

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 9, 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

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

FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

CVS Health Children's Nasal Saline Drops With Himalayan Salt Saline Nasal Moisturizer Single-Use 30 Single-Use 0.05 fl. oz. (1.5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, UPC 050428598207

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

DrKids Children's Natural Cough Syrup English Ivy Leaf Organic Agave Nectar Pre-measured Single-Use 0.17 fl. oz. (5 mL), Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, UPC 370302489019

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

CVS Health Children's Cough Syrup English Ivy Leaf Daytime Relief Natural Pineapple Flavor 20 Single-Use 0.08 fl. oz. (2.5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 050428597958

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

DrKids Children's Cough & Chest Congestion DM, Dextromethorphan HBr 5 mg Guaifenesin 100 mg Mixed Berry Flavor 20 Pre-measured Singe-Use 0.17 fl. oz. (5 mL), Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, NDC 70302-013-20, UPC 370302268010

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

CVS Health Children's Allergy Relief Liquid Medication Diphenhydramine HCl 12.5 mg/5 mL Oral Solution Antihistamine Mixed Berry Flavor 20 Single-Use 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC 69842-261-01, UPC 050428597156

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

DrKids Children's Pain & Fever Oral Solution Acetaminophen 160 mg/5 mL, 20 Pre-measured Single-Use Vials 0.17 fl. oz. (5 mL), Cherry Flavor, Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, NDC 70302-011-20, UPC 370302223019

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL Antihistamine, 20 Pre-measured Single-Use Vials, 0.17 fl. oz. (5 mL), Mixed Berry, Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, NDC 70302-012-20, UPC 370302255010

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

CVS Health Children's Mucus Relief Chest Congestion Plus Cough Dextromethorphan HBr Cough Suppressant Guaifenesin Expectorant Mixed Berry Flavor 20 Singe-Use Vials Per Carton 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC 69842-260-01, UPC 050428597675

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 25, 2020Historical recordClass II

CVS Health Children's Pain & Fever Acetaminophen 160 mg/5 mL Pain reliever/Fever reducer Single-Use Vials Cherry Flavor 20 Single-Use Vials per carton 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC 69842-0258-01, UPC 050428601891

by Unipharma, Llc.

Reason: CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 7, 2023Historical recordClass I

Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020

by D.B.P. Distribution

Reason: Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 26, 2021Historical recordClass III

Relpax (eletriptan HBr) 40 mg, a) 12 tablets 2 cards x six 40 mg tablets per blister pack, NDC 0049-2340-05; b) 6 tablets 1 card x six 40 mg tablets per blister pack, NDC 0049-2340-45, Rx Only, Made in Ireland, Distributed by Roerig, Division of Pfizer Inc, NY NY 10017.

by Pfizer Inc.

Reason: Labeling: Label Error on Declared Strength: an artwork error on the secondary packaging of Relpax 40 mg Tablets, indicates that each tablet contains eletriptan hydrobromide equivalent to 20mg eletriptan, instead of 40mg, on one side of the carton.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 12, 2019Historical recordClass II

AmeriHerb International Inc

Product: Goldenseal herb c/s, Hydrastis Canadensis, Not for use durin…
Reason: Dried spice and herb products potentially contaminated with generic E. coli.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 12, 2019Historical recordClass II

AmeriHerb International Inc

Product: Lemon balm leaf c/s, Melissa officinalis, 1# Net, AmeriHerb…
Reason: Dried spice and herb products potentially contaminated with generic E. coli.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 12, 2019Historical recordClass II

AmeriHerb International Inc

Product: Mullein leaf c/s, Verbascum Thapsus, 1# Net, AmeriHerb LLC,…
Reason: Dried spice and herb products potentially contaminated with generic E. coli.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 12, 2019Historical recordClass II

AmeriHerb International Inc

Product: Dill weed c/s, Anethum graveolens, 1# Net, AmeriHerb LLC, Am…
Reason: Dried spice and herb products potentially contaminated with generic E. coli.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 12, 2019Historical recordClass II

AmeriHerb International Inc

Product: Blessed thistle herb c/s, Centaurea benedicus, Not for use d…
Reason: Dried spice and herb products potentially contaminated with generic E. coli.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 12, 2019Historical recordClass II

AmeriHerb International Inc

Product: Parsley flakes, Petroselinum sativum, 1# Net, AmeriHerb LLC,…
Reason: Dried spice and herb products potentially contaminated with generic E. coli.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical recordClass III

Barlean's Llc

Product: Item FG 10079, Barleans, Flax Oil, 100 Softgels per bottle.…
Reason: Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical recordClass III

Barlean's Llc

Product: Item FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg…
Reason: Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published: May 22, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical recordClass III

Barlean's Llc

Product: Item FG 10190, Barleans Full Spectrum Hemp Extract, 60 Softg…
Reason: Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Published: May 22, 2019
Distribution: Nationwide

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Data last updated: November 9, 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.