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Recall totals

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

37,448

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/snack-right-super-foods-inc-dba-brads-raw-chips-recalls-brads-crunchy-kale-veggie-chips-duePublished November 2, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 4, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Dibutyl Squaric Acid, Topical Solution (PF), Multiple Dose Vial, 2%, 10 mL per vial, Edge Pharma, LLC, 856 Hercules Dr, Colchester VT, 05446, NDC 05446-1047-03

by Edge Pharma, LLC

Reason: CGMP Deviations
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Dexamethasone sodium phosphate 0.4%, 120 mL per bottle, Multiple Dose Container For Topical Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-0622-01

by Edge Pharma, LLC

Reason: CGMP Deviations
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

CSF-HC Otic Insufflation Capsule, Sulfacetamide Sodium/Ciprofloxacin/Hydrocortisone/Amphotericin B Otic Powder, 50mg/ 30mg/ 25mg/ 5mg, 5 count bottle, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1634-01

by Edge Pharma, LLC

Reason: CGMP Deviations
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

CSF Otic Insufflation Capsule, Sulfacetamide Sodium/ Ciprofloxacin/ Amphotericin B Otic Powder, 50mg / 30mg / 5mg, 5 count bottle, For Otic Use with Insufflator, Edge Pharma, LLC 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1633-05

by Edge Pharma, LLC

Reason: CGMP Deviations
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Cantharidin PLUS, Cantharidin/Salicylic Acid Gel-Forming Suspension, 10 mL per vial, Multiple Dose Vials for Topical Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT, 05446, NDC 05446-0970-03

by Edge Pharma, LLC

Reason: CGMP Deviations
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Cantharidin Gel-Forming Suspension, 0.7%, 10 mL per vial, Multiple Dose Vial for Topical Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05546 NDC 05446-0572-03

by Edge Pharma, LLC

Reason: CGMP Deviations
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

BLT Topical Cream, Benzocaine/Lidocaine/Tetracaine, 20%/8%/4%, 60gm per jar, Multiple Dose Container For Topical Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT, 05446, NDC 05446-1235-01

by Edge Pharma, LLC

Reason: CGMP Deviations
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Vancomycin HCl in 0.9% Sodium Chloride Injection, USP, 1,750mg/500mL, Single Use Bag for IV Injection (Preservative Free), 500 mL pre-filled bag, Rx Only, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446 NDC 05446-1459-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Vancomycin HCl in 0.9% Sodium Chloride Injection, 1,500 mg/500 mL, USP, Single Use Bag for IV Injection (Preservative Free), 500 mL pre-filled bag, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1458-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Vancomycin HCl in 0.9 % Sodium Chloride Injection, USP, 1,250 mg/250 mL, Single Use Bag for IV Injection (Preservative Free), 250 mL pre-filled bag, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1456-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Vancomycin HCl, Sterile Ophthalmic Solution for Injection, Preservative Free, 8 mg/0.8mL (10 mg/mL) (vancomycin equivalent), 0.8 mL per syringe, Single Use Syringe, For Intraocular Injection, Edge Pharma LLC, 856 Hercules Dr., Colchester, VT, 05446, NDC 05446-0736-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Betadine (povidone-iodine), Sterile Ophthalmic Solution, Preservative Free, 5% 0.5mL per syringe, Single Use Syringe, For Topical Ophthalmic Use, Edge Pharma, LLC, 656 Hercules Dr., Colchester, VT 05446, NDC 05446-1680-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Phenylephrine HCl/Tropicamide/Cyclopentolate HCl/ Ketorolac Sterile Ophthalmic Solution, 10%/ 0.25%/ 0.25%/0.125%, 10 mL per dropper, Multiple Dose Droptainer for Topical Ophthalmic Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT, NDC 05446-0859-03

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Phenylephrine HCl/Tropicamide/Cyclopentolate HCl/Ketorolac Sterile Ophthalmic Solution, 2.5%/0.25%/0.25%/0.125%, 0.5 mL syringe, Single Use Syringe, For Topical Ophthalmic Use, NDC 05446-0993-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Phenylephrine HCl/Tropicamide, Sterile Ophthalmic Solution, 2.5%/1%, 15 mL per dropper, Multiple Dose Droptainer for Topical Ophthalmic Use, Edge Pharma, LLC, 856 Colchester, VT 05446, NDC 05446-0815-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Phenylephrine HCl/Lidocaine, Sterile Ophthalmic Solution for Injection, Preservative Free, 1.5%/1%, 0.8mL per syringe, Single Use Syringe For Intraocular Injection, Edge Pharma LLC, 856 Hercules Dr, Colchester, VT 05446, NDC 05446-1118-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

PHENYLephrine, 0.9% Sodium Chloride Injection, USP, 20 mg/250mL, (0.08 mg/mL), Single use bag for IV injection (Preservative Free), Rx Only, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT NDC 05446-1667-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Phenylephrine HCl, Sterile Solution for Injection, (PF), 800 mcg/10mL (80 mcg/mL), Single Use Syringe for IV Injection, Edge Pharma, LLC 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1652-01

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Phenylephrine HCl, 1mg/10mL (0.1mg/mL), 10 mL per syringe, Single Use Syringe for IV Injection, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT 05446 NDC 05446-1544-10

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Phenylephrine HCl 0.5 mg/5mL, (0.1 mg/mL), 5 mL per syringe, Single Use Syringe for IV Injection, Edge Pharma, LLC, 856 Hercules Dr, Colchester, VT 05446, NDC 05446-1545-05

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility
Published: February 2, 2022
Distribution: Nationwide

View recall →

Data last updated: November 4, 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.