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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 14, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall United States Ongoing Historical recordClass I

Abbott Laboratories

Product: Abbott Similac Human Milk Fortifier 0.9g Pouch / Sachet, 50…
Reason: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
Published: March 16, 2022
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass I

Abbott Laboratories

Product: Abbott EleCare Infant Formula Unflavoured 400g can. 6 cans…
Reason: Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced
Published: March 16, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

DEL MONTE FOODS INC

Product: Del Monte Bubble Fruit - Tropical Mixed Fruit Cup Snacks. Mi…
Reason: Product being recalled due to potential metal fragment approximately 2-3mm in size.
Published: March 16, 2022
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

FACTOR

Product: Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tr…
Reason: Undeclared Milk Allergen
Published: March 16, 2022
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

El Chavito

Product: El Chavito¿ Saladitos Enchilados Salted Plums with Chili, ne…
Reason: Potential to be contaminated with lead.
Published: March 16, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

El Chavito

Product: El Chavito¿ Saladitos Dried Salted Plums, net wt. 1.7 oz bag…
Reason: Potential to be contaminated with lead.
Published: March 16, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053, NDC 60432-466-08.

by Morton Grove Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications: higher than permissible levels of unknown impurities were found in the drug product.
Published: March 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) 30 tablets per bottle, NDC: 68788-6381-03, b) 60 tablets per bottle, NDC: 68788-6381-06, c) 90 tablets per bottle, NDC: 68788-6381-09, Mfg: Par Pharmaceutical.

by Preferred Pharmaceuticals, Inc.

Reason: CGMP deviations
Published: March 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Olanzapine Tablets, USP 10 mg, 30-count bottles, Rx only, Manufactured for: Macleods Pharma USA , Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd., Baddi, HImachal Pradesh, India, NDC 33342-070-07.

by Macleods Pharma Usa Inc

Reason: cGmp Deviations
Published: March 9, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Luxury 70% Isopropyl Alcohol, 16 FL. OZ. (1PT) 473 ML bottle, Distributed by: TSM Brands LLC, 540 Equinox Ln, Manalapan, NJ 07726, UPC 868275965734.

by Tsm Brands LLC

Reason: Labeling - product contains undeclared ethyl alcohol
Published: March 9, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen, 12 FL. OZ. 355 ML bottle, Distributed By: TSM Brands LLC, 540 Equinox LN, Manalapan, NJ 07726, www.tsmbrands.com, Made in Turkey, UPC 868275965765

by Tsm Brands LLC

Reason: Labeling - product contains undeclared ethyl alcohol
Published: March 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amlodipine and Olmesartan Medoxomil Tablets, 10 mg /20 mg, 30-count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc., Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals, Ltd, Baddi, Himachal Pradesh, INDIA, NDC 33342-192-07.

by Macleods Pharma Usa Inc

Reason: cGMP deviations
Published: March 9, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Vadilal Industries USA Inc.

Product: Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz…
Reason: Product may be contaminated with Salmonella
Published: March 9, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

J & M Foods, Inc.

Product: Favorite Day Carrot cake soft bake cookies Net Wt 8 oz. (227…
Reason: Pecans although listed in the Ingredient Statement, was omitted from the CONTAINS statement.
Published: March 9, 2022
Distribution: Multiple states

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FDA Recall Ongoing Historical recordClass II

Premium Nature Instant Hand Sanitizer, (ethyl alcohol 70%), plastic bottle packaged as (a) 8 OZ, UPC 8 19192 02866 8; (b) 16 OZ, UPC 8 19192 02874 3; Premium Nature, South Plainfield, NJ.

by AMS Packaging Inc

Reason: Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), plastic bottles packaged as (a) 2 OZ / 60ML, UPC 8 19192 02865 1; (b) 4 OZ, 118 ML, UPC 8 19192 02826 2; (c) 16 OZ, 473 ML, UPC 8 19192 02874 3; (d) 1 gallon, UPC 8 19192 02830 9; Premium Nature, South Plainfield, NJ.

by AMS Packaging Inc

Reason: Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

RISE UP RED EDITION Capsules, 650 mg, 10-count blisters packaged in a carton, ASIN B08JCWG84D, barcode X002NI8PE1.

by Positive Health

Reason: Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Sapropterin Dihydrochloride Powder for Oral Solution, 100 mg, 30 individual packets per carton, Rx Only, Dr. Reddy's, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC: 43598-477-11 (packet), 43598-477-30 (carton).

by Dr. Reddy's Laboratories, Inc.

Reason: Subpotent Drug: Out-of-specification results observed in Assay in sapropterin dihydrochloride powder 100mg.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant with Menthol, 1 FL Oz (30 mL) per bottle, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544. NDC 41250-989-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant with Menthol, 1 FL Oz (30 mL) per bottle, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544. NDC 41250-989-10

by Perrigo Company PLC

Reason: CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published: March 2, 2022
Distribution: Nationwide

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Data last updated: September 14, 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.