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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

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 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

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

FDA Recall TerminatedTerminated: December 15, 2017Historical recordClass III

Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-370-01.

by Alvogen, Inc

Reason: Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published: April 12, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 15, 2017Historical recordClass III

Nifedipine Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-369-01.

by Alvogen, Inc

Reason: Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published: April 12, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 15, 2017Historical recordClass III

Adalat CC (nifedipine) Extended Release Tablets, 60 mg, 100- count bottles, Rx only Manufactured for Almatica, Almatica Pharma Inc. Pinebrook, NJ 07058 USA, NDC 50419-702-05

by Alvogen, Inc

Reason: Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published: April 12, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 15, 2017Historical recordClass III

Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles, Rx only, Manufactured for Bayer Healthcare Bayer Healthcare Pharmaceuticals Inc. Whippany, NJ 07901 Manufactured in Germany, NDC 50419-701-05

by Alvogen, Inc

Reason: Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published: April 12, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 15, 2017Historical recordClass III

Nifedipine Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-368-01.

by Alvogen, Inc

Reason: Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published: April 12, 2017
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 22709, NDC 0173-0682-20.

by GlaxoSmithKline, LLC

Reason: Defective Delivery System: Elevated number of units with out of specification results for leak rate.
Published: April 12, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 25, 2021Historical recordClass II

Kalbitor (ecallantide), 10mg/mL, packaged in 3 vials per Carton, Rx Only, Dynax Corp., Burlington, MA. NDC47783-101-01

by Shire

Reason: Presence of Particulate Matter: Glass
Published: April 12, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 19, 2018Historical recordClass II

Ikea North America Srvcs Inc

Product: Choklad Not; Milk Chocolate with hazelnut Net Wt 3.5 OZ;…
Reason: IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. CHOKLAD N¿T Milk Chocolate with Hazelnut, 3.5 oz. (100g), UPC: 120293926000: the manufacturing process adds the undeclared ingredient almond to the product. The labeling carries a "May Contain" statement identifying Almond.
Published: April 12, 2017
Distribution: AZ CA Co CT FL GA IL KS MA MD…

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FDA Recall United States TerminatedTerminated: January 19, 2018Historical recordClass II

Ikea North America Srvcs Inc

Product: Choklad Ljus Milk Chocolate Net Wt 3.5 OZ; IKEA Produce…
Reason: IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. CHOKLAD LJUS Milk Chocolate Bar, 3.5 oz. (100g), UPC: 1402939250003; the manufacturing process adds the undeclared ingredients Hazelnut and Almond . The labeling carries a "May Contain" statement identifying almond and hazelnuts.
Published: April 12, 2017
Distribution: AZ CA Co CT FL GA IL KS MA MD…

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FDA Recall United States TerminatedTerminated: January 19, 2018Historical recordClass II

Ikea North America Srvcs Inc

Product: Godis Chokladran Wafers filled and covered with Milk chocol…
Reason: IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. GODIS CHOKLADRAN Wafer Filled and Covered with Chocolate, 5.9 oz. (168g), UPC: 1202290300009, the ingredient statement fails to declare Hazelnut and Almond. The manufacturer's process adds hazelnut and almond to the product. The product labeling does include a "May Contains" statement identifying "tree nuts". This statement does not declare the almond and hazelnut.
Published: April 12, 2017
Distribution: AZ CA Co CT FL GA IL KS MA MD…

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FDA Recall United States TerminatedTerminated: January 19, 2018Historical recordClass II

Ikea North America Srvcs Inc

Product: Godis Chokladkrokant Milk chocolate with butterscotch pieces…
Reason: IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. GODIS CHOKLADKROKANT Milk Chocolate with Butterscotch, 15.9 oz. (450g); UPC: 1202155040002, as manufactured was found to contain undeclared ingredients: Hazelnut, Almond. Labeling does include a "May Contain" statement identifying: Almonds and Hazelnuts.
Published: April 12, 2017
Distribution: AZ CA Co CT FL GA IL KS MA MD…

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FDA Recall United States TerminatedTerminated: January 19, 2018Historical recordClass II

Ikea North America Srvcs Inc

Product: Choklad Lingon & Blabar Assortment of milk chocolate Squares…
Reason: IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. CHOKLAD LINGON & BLABAR, 6.3 0z (180g), UPC: 1602184210009. Due to manufacturing process, the product contains the undeclared ingredients Hazelnut and Almond. The labeling carries a "May Contain" statement identifying Almonds and Hazelnuts.
Published: April 12, 2017
Distribution: AZ CA Co CT FL GA IL KS MA MD…

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FDA Recall United States TerminatedTerminated: January 19, 2018Historical recordClass II