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Recall totals

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

37,450

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresh-ready-foods-llc-recalls-fresh-you-brand-sausage-egg-cheese-biscuit-sandwich-due-possiblePublished November 8, 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 United States TerminatedTerminated: July 5, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: Whole Foods Market, TART LEMON SMALL
Reason: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.
Published: February 22, 2017
Distribution: According to the firm the product was di…

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FDA Recall United States TerminatedTerminated: July 5, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: Whole Foods Market, TART FRENCH APPLE SMALL
Reason: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.
Published: February 22, 2017
Distribution: According to the firm the product was di…

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FDA Recall United States TerminatedTerminated: July 5, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: Whole Foods Market, TART PEANUT BUTTER CHOCOLATE
Reason: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.
Published: February 22, 2017
Distribution: According to the firm the product was di…

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FDA Recall United States TerminatedTerminated: July 5, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: Whole Foods Market, SMALLTART FRESH BERRY SMALL, TART FRESH…
Reason: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.
Published: February 22, 2017
Distribution: According to the firm the product was di…

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FDA Recall United States TerminatedTerminated: July 5, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: Whole Foods Market, TART CHOCOLATE GANACHE SMALL, TART CHOCO…
Reason: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.
Published: February 22, 2017
Distribution: According to the firm the product was di…

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FDA Recall United States TerminatedTerminated: July 5, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: Whole Foods Market, TART KEY LIME 4IN TART KEY LIME 4IN,TAR…
Reason: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.
Published: February 22, 2017
Distribution: According to the firm the product was di…

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FDA Recall United States TerminatedTerminated: July 5, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: Whole Foods Market, TART FRUIT 4IN
Reason: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.
Published: February 22, 2017
Distribution: According to the firm the product was di…

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FDA Recall United States TerminatedTerminated: July 5, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: Whole Foods Market, TART FRESH FRUIT AMERO SHELL LARGE
Reason: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.
Published: February 22, 2017
Distribution: According to the firm the product was di…

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FDA Recall TerminatedTerminated: June 15, 2022Historical recordClass III

Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9; Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-3075-3.

by Apotex Inc.

Reason: Superpotent Drug: Product may not meet specifications throughout shelf life.
Published: February 15, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 29, 2020Historical recordClass III

Pantoprazole Sodium for Injection, 40mg per vial, Single-dose vial, Rx only, Mfd. in India for: Auromedics Pharma LLC 6 Wheeling Road, Dayton, NJ 08810, NDC 55150-202-00

by Aurobindo Pharma USA Inc

Reason: Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.
Published: February 15, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 24, 2017Historical recordClass III

Olanzapine tablets, USP, 2.5 mg, packaged in a 30-count bottle, Rx only, Mfd: By: Dr. Reddy's Laboratories Limited, Bachupally, India, NDC 55111-163-30

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: due to out-of-specification result for the Related Substance Compound C (Impurity 6 - N-Oxide at the 18 month stability station.
Published: February 15, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 10, 2018Historical recordClass I

Dutch Valley Food Distributors Inc.

Product: Cappuccino Snack Mix Lot code: 20161027; Best By: 05/25/17…
Reason: As a result of an ingredient supplier recall, Dutch Valley is issuing a recall on Cappuccino Snack Mix due to the potential for it to be contaminated with Salmonella.
Published: February 15, 2017
Distribution: DE FL GA IA ID IL IN KS MA MD…

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Methadone Hydrochloride Oral Concentrate, USP 5 mg/5 mL C-II, 500 mL, 6 bottles per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-711-16.

by VistaPharm, Inc.

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published: February 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II (Sugar Free), 1 liter (1000 mL), 4 bottles per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-695-79.

by VistaPharm, Inc.

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published: February 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II, a.) 1 fl. oz. (30 mL), 12 bottles per case (NDC No. 66689-695-30), b). 1 liter (1000 mL), 4 bottles per case, (NDC No. 66689-695-79), Rx only, Manufactured by VistaPharm, Largo, FL 33771.

by VistaPharm, Inc.

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published: February 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Oxycodone Hydrochloride Oral Solution, USP 5 mg/5 mL, a). 5 mL, 50 unit dose cups of 5 mL per case (NDC No. 66689-401-50), b). 500 mL, 12 bottles per case (NDC No. 66689-403-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771.

by VistaPharm, Inc.

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published: February 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Lactulose Solution, USP 10 g/15 mL, 50 unit dose cups of 15 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-039-50.

by VistaPharm, Inc.

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published: February 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Lactulose Solution, USP 20 g/30 mL, 50 unit dose cups of 30 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-038-50.

by VistaPharm, Inc.

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published: February 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Nystatin Oral Suspension, USP 500,000 Units/5 mL, a). 50 unit dose cups of 5 mL per case (NDC No. 66689-037-50), b). 100 unit dose cups of 5 mL per case (NDC 66689-037-99), Rx only, Manufactured by VistaPharm, Largo, FL 33771.

by VistaPharm, Inc.

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published: February 8, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Phenytoin Oral Suspension, USP 100 mg/ 4 mL, 50 unit dose cups of 4 mL per case., Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-036-50.

by VistaPharm, Inc.

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published: February 8, 2017
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.