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Recall totals

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

37,497

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,881

Class I recallsReasonable probability of serious health consequences

24,543

Class II recallsTemporary or medically reversible health consequences

2,935

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 2,098 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 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 11, 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	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: November 3, 2016Historical recordClass I

Bounce Life Style HQ

Product: Australia -Cashew Cinnamon - Caf¿ Bounce, each bulk bag cont…
Reason: Cashew Cinnamon - Caf¿ Bounce is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 3, 2016Historical recordClass I

Bounce Life Style HQ

Product: US - Bounce Apple Cinnamon Protein Punch Energy Balls (old n…
Reason: Apple Cinnamon Protein Punch Energy Ball product is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta.
Published: October 5, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 6, 2017Historical recordClass II

Faribault Foods, Inc

Product: No-Salt-Added Black Beans, 15 oz. (425 g), packaged under th…
Reason: Faribault Foods is recalling 15 oz.No-Salt-Added Black Beans due to potential presence of plastic and/or metal pieces.
Published: October 5, 2016
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: February 17, 2017Historical recordClass II

WHOLE FOODS MARKET

Product: 365 Everyday Value Mango Frozen Fruit Bars 4 Bars-4 fl. oz.…
Reason: Undeclared coconut
Published: October 5, 2016
Distribution: AL, AZ, AR, CA, CO, CT, DC, FL, GA, HI,…

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FDA Recall TerminatedTerminated: April 19, 2018Historical recordClass III

Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial, Rx Only, For Subcutaneous Injection only, Manufactured by: Genzyme Corporation, 500 Kendall Street, Cambridge, MA 02142 A Sanofi Company Country of Origin : United Kingdom, NDC 0024-5862-01

by Genzyme Corporation / Genzyme Biosurgery

Reason: Labeling: Incorrect or Missing Lot and/or Exp. Date
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 15, 2017Historical recordClass III

Escitalopram Tablets USP 20 mg, 100-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Baltimore, MD, 21202, Manufactured by: Lupin Limited, Goa 403 722, India, NDC 68180-136-01

by Lupin Limited

Reason: Labeling: Incorrect or Missing Lot and/or Expiration Date
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 1, 2017Historical recordClass III

Amoxicillin For Oral Suspension, USP - Dye Free, 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: Hikma Pharmaceuticals, PO Box 182400, Amman 11118 - Jordan, Distributed by: West-Ward Pharmaceutical Corp. Eatontown, NJ 07724, NDC 00143-9887-01,

by West-Ward Pharmaceuticals Corp.

Reason: Labeling: Label Error on Declared Strength- bottles missing colored coded panel where strength of the product is displayed.
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 12, 2017Historical recordClass II

Phenylephrine HCI Injection, USP, 10mg/mL, packaged in a) 5 mL Vial, 50 mg/5 mL (NDC 66758-016-03), 25 x 5 mL Vials per carton (NDC 66758-016-04) and b) 10 mL Vials, 100 mg/10 mL (NDC 66758-017-01), Rx only, Manufactured for: Sandoz Inc., Princeton, NJ 08540.

by Sandoz Inc

Reason: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that product sterility may be compromised.
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 12, 2017Historical recordClass II

Ephedrine Sulfate Injection, USP, 50 mg/mL, 1 mL Fill in a 2mL Vial (NDC 66758-008-01), packaged in 25 x 2 mL Vials per carton (NDC 66758-008-02), Rx only, Manufactured for: Sandoz Inc., Princeton, NJ 08540.

by Sandoz Inc

Reason: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing firm raised concerns that product sterility may be compromised.
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 26, 2018Historical recordClass III

Carvediol Tablets, USP, 25 mg, 100-count bottle (NDC 57664-247-88), 500-count bottle (NDC 57664-247-13), 1000-count bottle (NDC 57664-247-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 26, 2018Historical recordClass III

Carvediol Tablets, USP, 12.5 mg, 500-count bottle (NDC 57664-245-13), 1000-count bottle (NDC 57664-245-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 26, 2018Historical recordClass III

Carvediol Tablets, USP, 6.25 mg, 100-count bottle (NDC 57664-244-18), 500-count bottle (NDC 57664-244-13), 1000-count bottle (NDC 57664-244-18), Rx Only, Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 26, 2018Historical recordClass III

Carvediol Tablets , USP, 3.125 mg, 100-count bottle (NDC 57664-242-88). 500-count bottle (NDC 57664-242-13), 1000-count bottle (NDC 57664-242-18), Rx Only Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512

by Sun Pharmaceutical Industries, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 30, 2017Historical recordClass II

CAMBRIDGE FARMS OF HANOVER LLC D

Product: Key Foods Soup Mix Vegetables, Key Foods Stores/ Staten Isla…
Reason: Firm was notified by North Carolina Dept. of Agriculture that a sample of Better Valu Cut Corn was found positive for Listeria monocytogenes. Firm initiated a recall based on the sample results.
Published: September 28, 2016
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: June 30, 2017Historical recordClass II

CAMBRIDGE FARMS OF HANOVER LLC D

Product: Giant Eagle Sweet & Savory Island Quinoa, Giant Eagle, Pitts…
Reason: Firm was notified by North Carolina Dept. of Agriculture that a sample of Better Valu Cut Corn was found positive for Listeria monocytogenes. Firm initiated a recall based on the sample results.
Published: September 28, 2016
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: June 30, 2017Historical recordClass II

CAMBRIDGE FARMS OF HANOVER LLC D

Product: Better Value Mix Vegetables, Federated Group, Inc./Arlington…
Reason: Firm was notified by North Carolina Dept. of Agriculture that a sample of Better Valu Cut Corn was found positive for Listeria monocytogenes. Firm initiated a recall based on the sample results.
Published: September 28, 2016
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: June 14, 2017Historical recordClass I

United Natural Trading

Product: Walnuts Halves & Pieces Net Wt. 2.5 lbs Distributed by Wood…
Reason: Walnut pieces may be contaminated with Listeria monocytogenes which was determined through Third Party Sampling.
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 14, 2017Historical recordClass I

United Natural Trading

Product: Woodstock Cape Cod Cranberry Mix Net Wt. 10 oz. Distributed…
Reason: Walnut pieces may be contaminated with Listeria monocytogenes which was determined through Third Party Sampling.
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 21, 2017Historical recordClass II

Immune Tree, Inc (formerly ITG, Inc.)

Product: LeptiTrim6 Vanilla Shake Item No. 9907; 860 g. Brand Immune…
Reason: Immune Tree is recalling certain Immune Tree; Health Works; Immune Pro6; Good For You and Surthrival brand colostrum products due to undeclared milk allergen.
Published: September 28, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 26, 2017Historical recordClass II

McCormick & Company - Corporate Headquarters

Product: ZATARAINS GUMBO PASTA DINNER 5.7 OZ PACKAGE
Reason: The Zatarains plant in Gretna, LA was contacted by General Mills to inform the plant that they were impacted by General Mills flour recall. Fifty (50) bags of WONDRA ENR 50 UNMALTED were shipped to Gretna in March 2016. This material has been used in the production of four different Zatarains brand pasta dinner mixes over several processing dates.
Published: September 28, 2016
Distribution: Product shipped to the following states:…

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Data last updated: November 11, 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.