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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

36,949
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/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-riskPublished September 4, 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 441–460 of 17,758 recalls

FDA Recall Ongoing 2026 recordClass II

Phenylephrine Hydrochloride Injectable Solution, 40mg, 250*mL Bag, wells pharma of Houston, NDC 73702-122-03

by Wells Pharma of Houston LLC

Reason
cGMP deviations.
Published
May 6, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

Similasan, iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, Distributed by: Thea Pharma Inc., Waltham, MA 02451, NDC 59262-700-11

by Thea Pharma, Inc.

Reason
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, Distributed by: Thea Pharma Inc., Waltham, MA 02451, NDC 82584-700-11

by Thea Pharma, Inc.

Reason
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Optase Dry Eye Intense Drops (Glycerin 0.2%), packaged in 0.33 fl oz, Sterile, Manufactured for Scope Health Inc., 79 Madison Ave., 8th Floor, New York, NY 10016, USA, NDC 72972-002-01.

by SCOPE HEALTH

Reason
Lack of Assurance of Sterility
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Levocarnitine Injection, USP, 1 g/5 mL (200 mg/mL), 5 mL Single-Dose Vial, For intravenous use, Rx Only, American Regent, Inc., Shirley, NY 11967. NDC: 0517-1045-01

by American Regent, Inc.

Reason
Labeling: Missing Label
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

GenTeal Tears, Lubricant Eye Gel, Sterile, 10g (0.34 Fl oz), Distributed by: Alcon Laboratories, Inc., Fort Worth, Texas 76134, USA, NDC: 0065-8064-01.

by Alcon Research LLC

Reason
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality.
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Systane, Lubricant Eye Gel, Night Gel, Sterile, 10g (0.35 oz), Processed in France for: Alcon Laboratiroes, Inc., Fort Worth, TX 76134, USA, NDC 0065-0474-01

by Alcon Research LLC

Reason
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality.
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

King Juice Company, Inc.

Product
Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UP…
Reason
Product contains undeclared Yellow No. 5.
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

The Mochi Ice Cream Company, LLC

Product
My Mochi Strawberry flavored Non-Dairy Frozen Dessert; 7.5 o…
Reason
Foreign object found inside retail container.
Published
May 6, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, NDC 0555-1054-56, with 10x10 blister packs NDC 0555-1054-60; b) 30-count carton, NDC 0555-1054-86, with 3X10 blister pack NDC 0555-1054-60; Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.

by Teva Pharmaceuticals USA, Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

LACTATED RINGER'S IRRIGATION, 3000 mL bags, Sterile, Ex only, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7389-60.

by B BRAUN MEDICAL INC

Reason
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

0.9 % SODIUM CHLORIDE IRRIGATION, USP, 3000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7388-60.

by B BRAUN MEDICAL INC

Reason
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7387-50.

by B BRAUN MEDICAL INC

Reason
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Published
April 29, 2026
Distribution
Nationwide

View recall →

FDA Recall Ongoing 2026 recordClass II

Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 18018-3524, NDC: 0264-7385-60.

by B BRAUN MEDICAL INC

Reason
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premier Medical Products, 1710 Romano Drive, Plymouth Meeting, PA 19462, NDC 48783-112-08.

by Premier Dental Products Co

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the vial itself; the saleable unit of the box of 12 bottles has the correct expiration date printed.
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.

by Harrow Eye LLC

Reason
Lack of Assurance of Sterility
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-118-01

by Leading Pharma, LLC

Reason
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Pantoprazole Sodium, Delayed-Release Tablets, USP, 40 mg, 1000-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, By: Hetero, Hetero Labs Limited, Unit V, Polepally, Jadcherta, Mahabubager-509 301, India, NDC 31722-713-10

by Hetero Labs Limited (Unit V)

Reason
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46288. NDC: 0904-7495-06

by The Harvard Drug Group LLC

Reason
Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.
Published
April 29, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

Marquez Brothers International, Inc.

Product
EL MEXICANO agua fresca de horchata Instant Horchata Drink N…
Reason
Undeclared milk.
Published
April 29, 2026
Distribution
Domestic distribution: AK, AL, AR, AZ, C…

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.