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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.

37,063
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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 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)

  • 1,527 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

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

Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 2,801–2,820 of 18,346 recalls

FDA Recall Terminated Historical recordClass II

PHENYLephrine in 0.9 sodium chloride, 800 mcg/10 mL, (80 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-6008-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

PHENYLephrine in 0.9 sodium chloride, 400 mcg/10 mL, (40 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6007-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

lidocaine 2%, 100 mg/5 mL, (20 mg/mL), 5 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6006-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

ePHEDrine in 0.9% sodium chloride, 50 mg/5 mL, (10 mg/mL), 5 mL Syringe, Rx only, CAPS Inc., Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-6004-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

ketamine in 0.9% sodium chloride, 50 mg/5mL (10mg/mL), 5 mL syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-3022-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL in 0.9% sodium chloride, 10 mcg/1 mL, (10 mcg/mL), 3 mL syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2071-7

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%), packaged in 90-count plastic jar, further packaged in case of 6 jars per case, Distributed by RB Health (US), Parsippany, NJ 07054, NDC 63824-431-90

by RB Health (US) LLC

Reason
Labeling: Label Error on Declared Strength: The incorrect label on the back of the product packaging.
Published
October 4, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Eligard (leuprolide acetate) for injectable suspension, 7.5 mg every month, Sterile, Rx Only, Must be reconstituted before use, NDC 62935-753-75, Manufactured by: Tolmar Inc., Fort Collins, CO 80526, For Tolmar Therapeutics Inc., Fort Collins, CO 80526.

by Tolmar, Inc.

Reason
Superpotent Drug - Higher than expected levels of leuprolide acetate in the constituted product.
Published
October 4, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ozona Organics LLC

Product
OZONA ORGANICS LIQUID PROBIOTICS & GO HEALTHY LIQUID PROBIOT…
Reason
Products contain high water activity in the formula that provides a potential for microbial growth.
Published
October 4, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Humanrace Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, packaged as a 148mL (5 fl oz.) bottle, PA ++++, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Squalene, Aloe, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-002

by HUMANRACE

Reason
Subpotent Drug: Product does not contain SPF that is declared on the label.
Published
September 27, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, packaged as a 53mL (1.8 fl oz.) bottle, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-01

by HUMANRACE

Reason
Subpotent Drug: Product does not contain SPF that is declared on the label.
Published
September 27, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936, NDC 0078-0110-22.

by Novartis Pharmaceuticals Corp.

Reason
Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals.
Published
September 27, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)), Rx only, Manufactured for Sun Pharma Global FZE by: Laboratoire Unither, Coutances, France NDC 47335-506-96

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Subpotent: Out of Specification result observed for low assay
Published
September 27, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Rasagiline Tablets 0.5mg, 30-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A., NDC 0378-1270-93

by Aurobindo Pharma USA Inc.

Reason
Failed dissolution specifications - results obtained were below spec average.
Published
September 27, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Sterile Solution, 0.03mL (1 ml) each, 60 applicators in carton, applicator is sterile if package is intact. CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co., NDC 54365-400-31 REF 930480 Product is packaged in the following manner: There is one (1) sterile applicator (sponge) per pouch. Each inner carton contains sixty (60) pouches. There are four (4) inner cartons per shipping case (total of 240 pouches per case).

by CareFusion 213, LLC

Reason
Stability data does not support expiry: Shelf-life of the impacted lots of BD ChloraPrep" Clear 1 mL Applicator cannot be substantiated beyond 12-months although labeled with 36-month expiry. Stability studies indicate that the impacted lots, if stored at 30¿C/75% relative humidity continuously beyond 12 months, may exhibit growth of Aspergillus penicillioides.
Published
September 27, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

octiq Lubricating Eye Drops, Dextran 70.01%, Hypromellose 0.3%, 0.5 FL OZ Each (2X 15 mL Bottles), Manufactured for Innovus Pharmaceuticals, Inc., Englewood, CO 80112, Made in Jordan, NDC:57483-610-15.

by AMMAN PHARMACEUTICAL INDUSTRIES

Reason
Lack of Assurance of Sterility
Published
September 27, 2023
Distribution
Product was distributed to two (2) direc…

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes, Twitching Relief, Sterile Eye Ointment, Homeopathic 0.33 FL OZ (10 mL), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502, NDC: 17312-099-15.

by AMMAN PHARMACEUTICAL INDUSTRIES

Reason
Lack of Assurance of Sterility
Published
September 27, 2023
Distribution
Product was distributed to two (2) direc…

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes, Stye Relief, Sterile Eye Ointment, Homeopathic 0.14 oz (4 grams), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502, NDC: 17312-014-13.

by AMMAN PHARMACEUTICAL INDUSTRIES

Reason
Lack of Assurance of Sterility
Published
September 27, 2023
Distribution
Product was distributed to two (2) direc…

View recall →

FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes, Red Eye Relief PF, Sterile Eye drops, Homeopathic 0.33 FL OZ (10 mL), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502 NDC: 17312-095-19.

by AMMAN PHARMACEUTICAL INDUSTRIES

Reason
Lack of Assurance of Sterility
Published
September 27, 2023
Distribution
Product was distributed to two (2) direc…

View recall →

FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes, Red Eye Relief, Sterile Eye drops, Homeopathic 0.33 FL OZ (10 mL), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502, NDC: 17312-058-15.

by AMMAN PHARMACEUTICAL INDUSTRIES

Reason
Lack of Assurance of Sterility
Published
September 27, 2023
Distribution
Product was distributed to two (2) direc…

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.