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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

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

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Source: FDA and USDA public dataLast updated September 6, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,263
Class I	9,732
Class III	2,873
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,263
Class I	9,732
Class III	2,873
Not Yet Classified	1

FDA Recall Ongoing 2026 recordClass II

Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Dry Eye Relief Revitalizing Formula, 10 ml (1/3 fl.oz.), Wizcure Pharmaa PVT. LTD., H-881, Phase 3, RIICO Industrial Area, Bhiwadi-301019, India, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ 85260, NDC 77790-003-10.

by Wizcure Pharmaa Private Limited

Reason: Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Vista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, 10 ml. (1/3 fl. oz), Wizcure Pharmaa PVT. LTD, H-881, Phase-3, RIICO Industrial Area, Bhiwadi-301019, India, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260, NDC 77790-002-10.

by Wizcure Pharmaa Private Limited

Reason: Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Vista Tears Polyethylene Glycol 400 0.4% w/v, Propylene Glycol 0.3% w/v Eye Drops, Dry Eye Relief, Lubricant Drops, Sterile 10 ml (1/3 fl. oz.), Manufactured by: RA/Drugs/ MFG/2019/196283, Omni Lens Pvt. Ltd. 5, Samrudhhi, Opposite:Sakar-III, Navrangpura, Ahmedabad-380014, INDIA. Manufactured for and distributed by hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260. NDC 77790-001-10.

by Wizcure Pharmaa Private Limited

Reason: Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Agebox iKids-Growth (Night Formula), 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 850065597027

by Agebox

Reason: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wilmington, DE 19801 USA, UPC 8 50065 59701 0

by Agebox

Reason: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass III

Eptifibatide Injection, 75 mg/100 mL vial for weight-adjusted bolus dosing, 1x100 mL Single-dose Vial, For Intravenous Use Only, Rx Only, Manufactured by: Hainan Poly Pharm. Co., Ltd., Guilinyang Economic Development Area, Haikou, Hainan Province, China 571127; Distributed by: Slate Run Pharmaceuticals, LLC, Columbus, Ohio 43215. NDC Slate Run Carton Label: 70436-027-80; NDC ProRx Carton Label: 70436-163-80

by Slate Run Pharmaceuticals

Reason: Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.

by AvKARE

Reason: Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Adbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single dose Autoinjector, SAMPLE NOT FOR SALE, NDC 50222-350-91; b) 2 x Single dose Autoinjectors, NDC 50222-350-02; Rx only, Manufactured by: LEO Pharma A/S. Industriparken 55, DK-2750 Ballerup, Denmark, Distributed by: LEO Pharma Inc., Madison, NJ 07940, USA,

by LEO PHARMA INC

Reason: Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

Gerber Products Company dba Nestle Infant Nutrition

Product: Gerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged…
Reason: Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
Published: March 4, 2026
Distribution: Nationwide

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FDA Recall United States Terminated 2026 recordClass I

Art Monkey LLC dba Why Not Natural

Product: Why Not Natural Moringa Capsules 120 capsule bottle marked w…
Reason: Potential to be contaminated with Salmonella
Published: February 25, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass I

UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041 Arco Corporate Drive, Suite 200, Raleigh, NC 27617, NDC 69448-025-63

by McKesson

Reason: Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated environment.
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90.

by Meitheal Pharmaceuticals, Inc

Reason: Defective Delivery System: Missing or duplicated needles within the injection kit
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11

by Amerisource Health Services LLC

Reason: Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

vancomycin HCl, 2 grams, 2 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-019-59.

by Fresenius Kabi Compounding, LLC

Reason: Lack of Assurance of Sterility
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

vancomycin HCl, 1.5 grams, 1.5 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-016-59

by Fresenius Kabi Compounding, LLC

Reason: Lack of Assurance of Sterility
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-079-56.

by Fresenius Kabi Compounding, LLC

Reason: Lack of Assurance of Sterility
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

ketamine HCl, 1,000 mg, 1,000 mg per 100 mL (10 mg per mL) in Sodium Chloride Injection, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-050-56

by Fresenius Kabi Compounding, LLC

Reason: Lack of Assurance of Sterility
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

acyclovir sodium, 200 mg, 200mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, For Intravenous Use, Single-Use Bag, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-035-56

by Fresenius Kabi Compounding, LLC

Reason: Lack of Assurance of Sterility
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Testosterone 100mg Anastrozole 4mg , 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-32

by F.H. INVESTMENTS, Inc. (dba Asteria Health)

Reason: Presence of Foreign substance - potential presence of metal particulate matter
Published: February 18, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Testosterone 87.5mg, Triamcinolone Acetonide17.5 mcg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-6087-32.

by F.H. INVESTMENTS, Inc. (dba Asteria Health)

Reason: Presence of Foreign substance - potential presence of metal particulate matter
Published: February 18, 2026
Distribution: Nationwide

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Data last updated: September 6, 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.