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Recall totals

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

37,139

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 25, 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 II

INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL), Rx Only, packaged in a) single dose vials, (NDC 52544-931-07), b) carton of 10 x 2 ml Single Dose Vials (NDC 52544-931-02) Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054, Manufactured by: Patheon Italia S.p.A. Ferentino, Italy 03013.

by ALLERGAN

Reason: Failed Stability Specifications: Product stability testing results did not meet specifications for iron content.
Published: March 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Acyclovir Tablets, USP, 400 mg, 50 Tablets (5 x 10) unit dose blisters [NDC 50268-061-11] per carton [NDC 50268-061-15], Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478

by Apace KY LLC

Reason: Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir tablets may contain Torsemide tablets in some of the blister cavities.
Published: March 7, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Seggiano Usa Inc.

Product: Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g,…
Reason: The Tuscan Kale Pesto was mislabeled as Seggiano Artichoke & Garlic Sauce & Spread and therefore, contains undeclared cashews.
Published: March 7, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Market of Choice Inc

Product: Sezam Kale Salad ingredient kits, net wt. 6.43 pound. Ingre…
Reason: Sezam Kale Salad kits, 6.43 lbs, are recalled due to undeclared egg. The wrong dressing packet was added to the Sezam Kale Salad kit and the dressing contains undeclared egg.
Published: March 7, 2018
Distribution: distributed in OR

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FDA Recall United States Terminated Historical recordClass II

Meijer Distribution, Inc

Product: Meijer Greek Yogurt 0% Blueberry 5.3 oz. The products are…
Reason: The firm is announcing a voluntary recall of select Meijer branded Greek and Low-fat yogurt as a precautionary measure due to the potential risk of small particles of glass.
Published: March 7, 2018
Distribution: Domestic: Meijer stores in Michigan, Ohi…

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FDA Recall United States Terminated Historical recordClass II

Meijer Distribution, Inc

Product: Meijer Greek Yogurt 0% Strawberry 5.3 oz. The products are…
Reason: The firm is announcing a voluntary recall of select Meijer branded Greek and Low-fat yogurt as a precautionary measure due to the potential risk of small particles of glass.
Published: March 7, 2018
Distribution: Domestic: Meijer stores in Michigan, Ohi…

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FDA Recall United States Terminated Historical recordClass II

Meijer Distribution, Inc

Product: Meijer Greek Yogurt 0% Vanilla 5.3 oz. The products are pac…
Reason: The firm is announcing a voluntary recall of select Meijer branded Greek and Low-fat yogurt as a precautionary measure due to the potential risk of small particles of glass.
Published: March 7, 2018
Distribution: Domestic: Meijer stores in Michigan, Ohi…

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FDA Recall United States Terminated Historical recordClass II

Meijer Distribution, Inc

Product: Meijer Greek Yogurt 0% Plain 5.3 oz. The products are pac…
Reason: The firm is announcing a voluntary recall of select Meijer branded Greek and Low-fat yogurt as a precautionary measure due to the potential risk of small particles of glass.
Published: March 7, 2018
Distribution: Domestic: Meijer stores in Michigan, Ohi…

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FDA Recall United States Terminated Historical recordClass II

Meijer Distribution, Inc

Product: Meijer Yogurt Blended Low-fat Blueberry 6 oz.The products ar…
Reason: The firm is announcing a voluntary recall of select Meijer branded Greek and Low-fat yogurt as a precautionary measure due to the potential risk of small particles of glass.
Published: March 7, 2018
Distribution: Domestic: Meijer stores in Michigan, Ohi…

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FDA Recall United States Terminated Historical recordClass II

Meijer Distribution, Inc

Product: Meijer Greek Yogurt 0% Black Cherry 5.3 oz. The products ar…
Reason: The firm is announcing a voluntary recall of select Meijer branded Greek and Low-fat yogurt as a precautionary measure due to the potential risk of small particles of glass.
Published: March 7, 2018
Distribution: Domestic: Meijer stores in Michigan, Ohi…

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FDA Recall United States Terminated Historical recordClass II

Margalaxy LLC

Product: Cosmic Crunch Granola, packaged in paper bag, net wt 10 oz.…
Reason: Cosmic Crunch Granola is recalled due to undeclared coconut flakes.
Published: March 7, 2018
Distribution: distributed in OR

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FDA Recall United States Terminated Historical recordClass II

Bell Plantation Inc.

Product: Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic…
Reason: Analytical results for generic non-pathogenic E. coli surpassed firm's in-house specifications for finished product..
Published: March 7, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

La Salsa Foods Inc

Product: Pepitas - International Food Court brand, Thai Sweet Chili R…
Reason: Pepitas, International Food Court brand, Thai Sweet Chili Roasted Pumpkin Seeds, 4oz. bags, is recalled due to undeclared soybean oil and soy lecithin.
Published: March 7, 2018
Distribution: distributed in OR and WA.

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FDA Recall Terminated Historical recordClass II

Fluticasone propionate USP (Micronized) for prescription compounding, packaged in a) 1g (NDC (58597-8276-1), b) 10g (NDC 58597-8276-3), c) 25g (NDC 58597-8276-4), d) 100g (NDC 58597-8276-6), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

by American Pharmaceutical Ingredients LLC

Reason: CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Published: February 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cyanocobalamin USP (Vitamin B12) for prescription compounding, packaged in a) 1g (NDC 58597-8044-1), b) 5g (NDC 58597-8044-2), c) 25g (NDC 58597-8044-4), d) 100g (NDC 58597-8044-6), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

by American Pharmaceutical Ingredients LLC

Reason: CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Published: February 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Methylcobalamin (Vitamin B12) for prescription compounding, packaged in a) 500mg (NDC 58597-8142-1); b) 1g (NDC 58597-8056-2); c) 5g (NDC 58597-8056-3); d) 10g (NDC 58597-8056-4), e) 25 g (NDC 58597-8056-4); f) 100g (NDC 58597-8056-6), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

by American Pharmaceutical Ingredients LLC

Reason: CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Published: February 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Biotin USP (Vitamin H) for prescription compounding, packaged in a) 500mg (NDC 58597-8142-1); b) 1g (NDC 58597-8142-2); c) 5g (NDC 58597-8142-3); d ) 25g (NDC 58597-8142-4), Rx only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

by American Pharmaceutical Ingredients LLC

Reason: CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Published: February 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ascorbic Acid USP, for prescription compounding, packaged in a) 100g (NDC 58597-8120-6); b) 500g (NDC 58597-8120-7); c) 1000g (NDC 58597-8120-8); d) 5000g (NDC 58597-8120-9); e) 25000g (NDC 58597-8120-3), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

by American Pharmaceutical Ingredients LLC

Reason: CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Published: February 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Verapamil HCl USP for prescription compounding, packaged in a) 100g (NDC 58597-8039-6); b) 500g (NDC 58597-8039-7); c) 1000g (NDC 58597-8039-8), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

by American Pharmaceutical Ingredients LLC

Reason: CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Published: February 28, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Vardenafil HCl USP (trihydrate) for prescription compounding, packaged in a) 5g (NDC 58597-8575-2); b) 100g (NDC 58597-8575-6);c) 500g (NDC 58597-8575-7); d) 1000g (NDC 58597-8575-8), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327

by American Pharmaceutical Ingredients LLC

Reason: CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Published: February 28, 2018
Distribution: Nationwide

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Data last updated: September 25, 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.