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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: AZ ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 12, 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 Ongoing Historical recordClass I

Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile Single Dose Container, Rx Only, Baxter USA, NDC 0338-0433-04

by Baxter Healthcare Corporation

Reason: Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

SSP America PHX, LLC

Product: Apple Danish in a clear plastic bag with a white paper label…
Reason: Allergens were declared but the finished product label incorrectly listed ingredients of Almond Croissant.
Published: September 11, 2024
Distribution: AZ

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FDA Recall United States Terminated Historical recordClass II

SSP America PHX, LLC

Product: Cheese Danish in a clear plastic bag with a white paper labe…
Reason: Finished product label stated cheese in the product name but did not declare milk in the ingredients or allergen statement.
Published: September 11, 2024
Distribution: AZ

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FDA Recall United States Terminated Historical recordClass III

SSP America PHX, LLC

Product: Almond Croissant in a clear plastic bag with a white paper l…
Reason: Finished product label stated almond in the product name but did not declare tree nuts or almonds in the ingredients or allergen statement.
Published: September 11, 2024
Distribution: AZ

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FDA Recall United States Terminated Historical recordClass II

SSP America PHX, LLC

Product: Pita Jungle Hummus & Pita Chips packaged as individual "snac…
Reason: Finished product label does not declare sesame which is an ingredient of hummus (tahini).
Published: September 11, 2024
Distribution: AZ

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FDA Recall United States Terminated Historical recordClass II

SSP America PHX, LLC

Product: Pita Jungle Cilantro Jalapeno Hummus & Pita Chips packaged a…
Reason: Finished product label does not declare sesame which is an ingredient of hummus (tahini).
Published: September 11, 2024
Distribution: AZ

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FDA Recall United States Terminated Historical recordClass II

SSP America PHX, LLC

Product: Pita Jungle Greek Salad packaged in 11.8oz plastic clamshell…
Reason: Finished product label stated feta but did not declare milk in the sub-ingredients or allergen statement.
Published: September 11, 2024
Distribution: AZ

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FDA Recall United States Terminated Historical recordClass I

Unilever North America Supply Chain Company, LLC

Product: Popsicle Jolly Rancher Frozen Confection Pop Net Wt 2.71 FL…
Reason: Undeclared milk
Published: September 11, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cefixime for Oral Suspension USP, 100 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-405-01

by Lupin Pharmaceuticals Inc.

Reason: Subpotent Drug- An out of specification ( OOS ) result observed in assay test during 18-month long term stability study.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

IBU Ibuprofen Tablets, USP, 400 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a) NDC 55111-682-01 - 100 Tablets per bottle, b) NDC 55111-682-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

IBU Ibuprofen Tablets, USP, 600 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-683-01 - 100 Tablets per bottle, b)NDC 5511-683-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

IBU Ibuprofen Tablets, USP, 800 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-684-01 - 100 Tablets per bottle, b)NDC 55111-684-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Indomethacin Extended-Release Capsules, USP, 75 mg, packaged in a) 60-count bottle (NDC 68462-325-60) and b) 90-count bottle (NDC 68462-325-90), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Plot No. 2 Phase-2, Pharma Zone, SEZ, Pithampur, Dist-Dhar, Madya Pradesh - 454775, India Mfg Llc. No: 25/9/2010, Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: Failed Dissolution Specifications: below specification results
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

NOW Foods

Product: NOW Real Foods Whole & Unsalted Raw Brazil Nuts 12oz. bag UP…
Reason: High mold, yeast, and total viable count
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Colonna Brothers Inc.

Product: Ground cinnamon. Supreme Tradition brand ground cinnamon p…
Reason: Elevated lead levels in cinnamon
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

J F C International Inc

Product: J-Basket Brand, Napa Kimchi, Net Wt. 14.1oz. plastic jar con…
Reason: High levels of Yeast growth and film on top of jarred Kimchi product.
Published: September 4, 2024
Distribution: Firm ships product to the following stat…

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FDA Recall United States Terminated Historical recordClass I

Prime Food Processing Corp.

Product: Prime Food brand Steam Bun with Egg Custard & Coconut Added;…
Reason: Products may contain undeclared sesame
Published: September 4, 2024
Distribution: AZ, CA, CO, CT, FL, GA, HI, IL, KS, KY,…

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FDA Recall United States Terminated Historical recordClass I

Prime Food Processing Corp.

Product: Prime Food brand Steam Bun with Egg Custard Added; 10pcs/pac…
Reason: Products may contain undeclared sesame
Published: September 4, 2024
Distribution: AZ, CA, CO, CT, FL, GA, HI, IL, KS, KY,…

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FDA Recall Ongoing Historical recordClass II

Timolol Maleate Ophthalmic Solution USP, 0.5%, packaged in: a) 5mL bottle (NDC 64980-514-05), and b) 10mL bottle (NDC 64980-514-01), Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey

by FDC Limited

Reason: Defective Container: patients are unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
Published: August 28, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

HAND-I-SAN, No-Rinse Hand Sanitizer (75% Isopropyl Alcohol), packaged in a) 3.78L (1-gallon jug packaged in a case of 4x1 gallon jugs), b) 18.92L (5-gallon pail), c) 208.19L (55-gallon drum), and d) 1040.98L (275-gallon tote), ZEE Company 3401 Cummings Road, Chattanooga, TN, 37419, NDC 86161-210

by Zeco LLC

Reason: CGMP Deviations: sterile water not used for production
Published: August 28, 2024
Distribution: Nationwide

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Data last updated: September 12, 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.