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Recall totals

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

37,212

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 6, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass I

Bounce Life Style HQ

Product: Bounce Energy Ball Cashew & Pecan Vitality Lift, each loose…
Reason: Bounce Energy Ball Cashew & Pecan Vitality Lift 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical recordClass III

Shearer's Snacks

Product: Keebler, Sugar Wafers, Vanilla, Net Wt 2.75 OZ (77 g), Made…
Reason: Sugar wafer cookies contain an ingredient that was recalled by the ingredient manufacturer due to the presence of extraneous foreign matter in the refined granulated sugar (ingredient in the finished product).
Published: September 28, 2016
Distribution: Distributed to customer distribution cen…

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FDA Recall United States Terminated Historical recordClass II

Coca-Cola Company (The)

Product: Huberts Lemonade Watermelon, 16 Fl. Oz. (473 ml), Manufactur…
Reason: The product may contain foreign material (glass) in some bottles.
Published: September 28, 2016
Distribution: CA, CO, CT, DE, FL, GA, IO, IL, IN, ME,…

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FDA Recall United States Terminated Historical recordClass II

Coca-Cola Company (The)

Product: Huberts Lemonade Strawberry, 16 Fl. Oz. (473 ml), Manufactur…
Reason: The product may contain foreign material (glass) in some bottles.
Published: September 28, 2016
Distribution: CA, CO, CT, DE, FL, GA, IO, IL, IN, ME,…

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FDA Recall United States Terminated Historical recordClass I

Ryszard Food Distributor, Inc.

Product: Novus Snack brand Golden Raisins, Net 10 oz., Product of U.S…
Reason: The product contained undeclared sulfites (1337.2 ppm) based on sampling and analysis by New York State Department of Agriculture and Markets.
Published: September 28, 2016
Distribution: Brooklyn, NY

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FDA Recall United States Terminated Historical 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 Terminated Historical 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 Terminated Historical recordClass III

Shearer's Snacks

Product: Family Gourmet, Sugar Wafers, Vanilla, Net Wt 8 OZ (227 g),…
Reason: Sugar wafer cookies contain an ingredient that was recalled by the ingredient manufacturer due to the presence of extraneous foreign matter in the refined granulated sugar (ingredient in the finished product).
Published: September 28, 2016
Distribution: Distributed to customer distribution cen…

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Data last updated: October 6, 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.