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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

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

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Source: FDA and USDA public dataLast updated September 11, 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 II

TRP Natural Eyes Dryness Relief, Sterile Eye Drops, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-178-15.

by Optikem International, Inc.

Reason: Lack of Assurance of Sterility
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Eye Twitching Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-040-15.

by Optikem International, Inc.

Reason: Lack of Assurance of Sterility
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Blur Relief, Sterile Eye Drops, Homeopathic 0.5 FL OZ (15mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-002-11.

by Optikem International, Inc.

Reason: Lack of Assurance of Sterility
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

TRP Natural Eyes Allergy Eyes Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-032-15.

by Optikem International, Inc.

Reason: Lack of Assurance of Sterility
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Betimol (timolol ophthalmic solution) 0.5%, 15mL bottles, Rx only, Manufactured for: Thea Pharma Inc. Lexington, MA 02420, NDC 82584-002-15

by Thea Pharma, Inc.

Reason: Lack of Assurance of Sterility: Out of specification for volume and compromised container closure.
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Chloride for Injection Concentrate USP, 500 mEq/250 mL (2 mEq/mL), 250 mL Bag, Rx only, B. Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-1944-20

by B. Braun Medical Inc

Reason: Lack of assurance of sterility: pinholes, within the blue label characters on the EXCEL bag, specifically within the dotted characters on the label, resulting in leaks.
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Febuxostat Tablets 80mg, RX Only, 30 Tablets per bottle, NorthStarx, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India, NDC 16714-060-01.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Febuxostat Tablets 40mg, RX Only, 30 Tablets per bottle, NorthStarx, Manufactured for: Northstar Rx LLC., Memphis, TN 38141 , Manufactured by: Sun Pharmaceutical Industries Limited Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India, NDC 16714-059-01.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Trader Joe's Company

Product: Trader Joe s Southwest Salad (SKU 56077) 9 oz.
Reason: L. mono contamination
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Trader Joe's Company

Product: Trader Joe s Elote Chopped Salad Kit (SKU 74768) 11.94 oz.
Reason: L. mono contamination
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Trader Joe's Company

Product: Trader Joe s Cilantro Salad Dressing (SKU 36420) Perishable…
Reason: L. mono contamination
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

House of Coffee Beans, Inc

Product: Coffee 5 pound bags, 2 pound bags, 1 pound bags, 12 ounce ba…
Reason: potential allergen contact with almonds, pecans and coconut.
Published: March 20, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Mercaptopurine Tablets, USP 50 mg, packaged in: a) 25-count bottle (NDC 69076-913-02), b) 250-count bottle (NDC 69076-913-25), Rx only, Manufactured for: Quinn Pharmaceuticals, Boca Raton, FL, www.quinnrx.com

by Stason Pharmaceuticals, Inc.

Reason: Failed Dissolution Specifications: results slightly under spec at at 9-months.
Published: March 13, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Clindamycin Phosphate Topical Solution USP, 1%, 60 mL bottle, Manufactured for: Glasshouse Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, L5N 6R8, NDC 71428-0003-60

by Contract Pharmaceuticals Limited Canada

Reason: Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.
Published: March 13, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Clindamycin Phosphate, Topical Solution USP, 1%, 60 mL, Rx Only, Manufactured for and Distributed by: Marlex Pharmaceuticals, Inc., New Castle, DE 19720, NDC 10135-0691-61

by Contract Pharmaceuticals Limited Canada

Reason: Defective Container: Out of specification for weight due to a slow leakage at the 12-month stability timepoint.
Published: March 13, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% (15mg/mL), 1 ml in a Single- Dose Vial, RX Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-090-42

by Denver Solutions, LLC DBA Leiters Health

Reason: Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Moxifloxacin 5mg/ml, 1 ml in a Single- Dose Vial, Rx Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-097-42

by Denver Solutions, LLC DBA Leiters Health

Reason: Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42

by Denver Solutions, LLC DBA Leiters Health

Reason: Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, mountain spring scent, 1250 mL cases, Seatex LLC, 445 TX Hwy 36 Rosenberg, YX 77471

by Seatex LLC

Reason: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033

by Seatex LLC

Reason: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published: March 6, 2024
Distribution: Nationwide

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Data last updated: September 11, 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.