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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 2,072 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 27, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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 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 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 Terminated Historical recordClass I

Eillien's Candies, Inc.

Product: Item # 413674, WIP SPORTSMAN MIX 25#, UPC 120046901. ( this…
Reason: Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.
Published: September 28, 2016
Distribution: IL, IA, MI, MN, NY, ND, OK, SD, TX, WI.

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FDA Recall United States Terminated Historical recordClass I

Eillien's Candies, Inc.

Product: Mae's Corner Market, HOLIDAY PARTY TRAY MIX 31.4.5OZ( 1 l…
Reason: Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.
Published: September 28, 2016
Distribution: IL, IA, MI, MN, NY, ND, OK, SD, TX, WI.

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FDA Recall United States Terminated Historical recordClass I

Eillien's Candies, Inc.

Product: Mae's Corner Market, FIJI MIX, 14 OZ(397 g) , UPC 0349524…
Reason: Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.
Published: September 28, 2016
Distribution: IL, IA, MI, MN, NY, ND, OK, SD, TX, WI.

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FDA Recall United States Terminated Historical recordClass I

Eillien's Candies, Inc.

Product: Mae's Corner Store, DELUX PARTY TRAY. 24.5 OZ(1 lb 8.5 oz)…
Reason: Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.
Published: September 28, 2016
Distribution: IL, IA, MI, MN, NY, ND, OK, SD, TX, WI.

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FDA Recall United States Terminated Historical recordClass I

Eillien's Candies, Inc.

Product: BULK - ROASTED & SALTED SUNFLOWER KERNELS 50#, UPC: 03495…
Reason: Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.
Published: September 28, 2016
Distribution: IL, IA, MI, MN, NY, ND, OK, SD, TX, WI.

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FDA Recall United States Terminated Historical recordClass I

Eillien's Candies, Inc.

Product: BLAIN'S FARM & FLEET SUNFLOWER KERNEL 2 OZ (57 g), UPC 03495…
Reason: Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.
Published: September 28, 2016
Distribution: IL, IA, MI, MN, NY, ND, OK, SD, TX, WI.

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FDA Recall United States Terminated Historical recordClass I

Eillien's Candies, Inc.

Product: BLAIN'S FARM & FLEET ROASTED/UNSALTED SUNFLOWER KERNEL 16 OZ…
Reason: Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.
Published: September 28, 2016
Distribution: IL, IA, MI, MN, NY, ND, OK, SD, TX, WI.

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FDA Recall United States Terminated Historical recordClass I

Eillien's Candies, Inc.

Product: BLAIN'S FARM & FLEET, The BIG GAME PARTY TRAY B 25 OZ, UPC…
Reason: Eillien's Candies was notified by Sunopta, an ingredient supplier that the sunflower kernels may be contaminated with Listeria monocytogenes. In turn Eillien's in recalling a number of products manufactured with Roasted Salted Sunflower Kernels and / or Roasted Unsalted Sunflower Kernels. There have been no reported illnesses to date.
Published: September 28, 2016
Distribution: IL, IA, MI, MN, NY, ND, OK, SD, TX, WI.

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Data last updated: September 27, 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.