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Recall totals

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

36,950
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
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 2,071 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% 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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 421–440 of 17,946 recalls

FDA Recall Ongoing 2026 recordClass II

Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, In Single-Dose kits containing: 8-mL vial of 30 mg strength, a pre-filled syringe containing 2 mL of diluent, one vial adapter, and one sterile 1¿ 19-gauge safety injection needle, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 69300 Greece, Manufactured For: TEVA Pharmaceuticals, Parsippany, NJ 07054. NDC Kit Carton: 0480-9262-08; Vial Label: 0480-9260-01; Tray Label: 0480-9262-08; Diluent Label: 0480-9263-21.

by Teva Pharmaceuticals USA, Inc

Reason
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Published
May 13, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl. oz. (10.5 mL) x 25 applicators per box. Carefusion 213, LLC, El Paso, TX 79912, subsidary of Becton Dickinson and Co. NDC 54365-014-41

by CareFusion 213, LLC

Reason
Lack of assurance of Sterility: potential product contamination
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL Applicators per carton. Carefusion 213 LLC, El Paso, TX 79912, NDC 54365-014-42.

by CareFusion 213, LLC

Reason
Lack of assurance of Sterility: potential product contamination
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Duloxetine Delayed-Release Capsules, 20 mg, Rx Only, 60 capsules, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-097-06.

by Ajanta Pharma Ltd.

Reason
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Duloxetine Delayed-Release Capsules, 60 mg, Rx Only, 30 capsules, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-099-03

by Ajanta Pharma Ltd.

Reason
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Duloxetine Delayed-Release Capsules, 30 mg, Rx Only, a) 90 Capsules, NDC 27241-098-09, b) 30 capsules, NDC 27241-098-03, c) 1000 Capsules, NDC 27241-098-10, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India

by Ajanta Pharma Ltd.

Reason
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 2.5% DEX. LM/LC, 2L 5PK, Part Number 054-20222, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.

by Fresenius Medical Care Holdings, Inc.

Reason
Lack of Assurance of Sterility: Potential leaks from perforations in bags.
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 1.5% DEX. LM/LC, 2L 5PK, Part Number 054-20221, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.

by Fresenius Medical Care Holdings, Inc.

Reason
Lack of Assurance of Sterility: Potential leaks from perforations in bags.
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

busPIRone Hydrochloride Tablets, USP, 5 mg, 500-count bottle, Rx Only, Manufactured by Unichem Laboratories LTD., Ind, Area, Meerut Road, Ghazibad - 201 003, India Manufactured for: Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ 08816, NDC 29300-244-05.

by Unichem Pharmaceuticals USA Inc.

Reason
Subpotent drug
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

Wehah Farms

Product
LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb)…
Reason
Potential contamination with foreign materials.
Published
May 13, 2026
Distribution
U.S. States: CA, CT, FL, IL, NC, NH, NY,…

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FDA Recall United States Ongoing 2026 recordClass I

French Broad Chocolate Factory

Product
french broad CHOCOLATE bette's bake sale (a multi-flavor bon…
Reason
Undeclared nut allergen (walnut) due to mislabeling. The product's printed tasting guide incorrectly identifies the Walnut Fudge and Peach Cobbler flavor chocolates (bonbons). Consumers relying on the printed materials could mistakenly consume a nut-containing bonbon.
Published
May 13, 2026
Distribution
Product was shipped to the following sta…

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FDA Recall United States Ongoing 2026 recordClass III

Falcon Trading Co., Inc.

Product
SunRidge Farms Organic SUNSET SOUP MIX CERTIFIED ORGANIC BY…
Reason
Potential contamination with pesticides, haloxyfop and thiamethoxam
Published
May 13, 2026
Distribution
U.S. Distribution: CA, CO, HI, MO, TX, V…

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FDA Recall United States Ongoing 2026 recordClass III

Falcon Trading Co., Inc.

Product
SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY…
Reason
Potential contamination with pesticides, haloxyfop and thiamethoxam
Published
May 13, 2026
Distribution
U.S. Distribution: CA, CO, HI, MO, TX, V…

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FDA Recall United States Ongoing 2026 recordClass III

Falcon Trading Co., Inc.

Product
SunRidge Farms Organic Black Beans CERTIFIED ORGANIC BY QAI…
Reason
Potential contamination with pesticides, haloxyfop and thiamethoxam
Published
May 13, 2026
Distribution
U.S. Distribution: CA, CO, HI, MO, TX, V…

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FDA Recall United States Terminated 2026 recordClass II

Green Organic Vegetables

Product
Woodstock Organic Shelled Edamame 10 oz. and 48 oz.
Reason
Foreign object: metal pieces
Published
May 13, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass III

Tops Markets LLC

Product
Christopher Ranch Peeled Garlic 6 oz.
Reason
The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm
Published
May 13, 2026
Distribution
Multiple states

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FDA Recall United States Terminated 2026 recordClass III

Tops Markets LLC

Product
Garland Fresh Peeled Garlic 6 oz. bag
Reason
The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm
Published
May 13, 2026
Distribution
Multiple states

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FDA Recall Ongoing 2026 recordClass II

Alendronate Sodium Oral Solution, 70 mg/75 mL, 75 mL, Rx only, 4 x 75 mL Single Dose Bottles, Distr. by: Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ 07922, NDC 0054-0282-59.

by Hikma Pharmaceuticals USA INC

Reason
This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side.
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950

by Water-Jel Technologies, LLC

Reason
Failed PH Specifications
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.

by Wells Pharma of Houston LLC

Reason
cGMP deviations.
Published
May 6, 2026
Distribution
Nationwide

View recall →

Data last updated:

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.