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Recall totals

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

37,059

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/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 8, 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 2026 recordClass II

BioGlo Fluorescein Sodium Ophthalmic Strips USP, 100 diagnostic strips, Manufactured by Omni Lens PVT. Ltd., 5 - Samrudhhi, Opp. Sakar-III, Navrangpura, Ahmedabad, Gujarat, India - 380014, Email:info@omnilens.in, Manufactured for & disibruted by: HUB Pharmaceuticals, LLC, 8767 E Via de Ventura #175, Scottsdale, AZ, 85258, NDC 17238-900-11.

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

Bio Glo Fluorescein Sodium Ophthalmic Strips USP, 300 diagnostic strips, Manufactured Omni Lens Pvt Ltd 5 - Samruddhi, Opp. Sakar - III, Navrangpura, Ahmedabad - 380014, India, Email:info@omnilens.in, Manufactured for & distributed by: HUB Pharmaceuticals, LLC, 8767 E Via de Ventura #175, Scottsdale, AZ, 85258, NDC 17238-900-30.

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

CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) 100-count box, NDC 83851-100-10; b) 300-count box, NDC 83851-100-30. Manufactured by Wizcure Pharmaa PVT. LTD, H-681, Phase 3, RIICO Industrial Area, Bhiwadi- 301019 INDIA, Vistamerica USA, 20 Perkins Dr. Prescott, AZ 86301, Vistamerica USA, Made in India,

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 Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP (Sterile Drops. Dry Eye Relief, 15 ml. (1/2 fl. oz.), Wizcure Pharmaa Pvt. Ltd., H-881, Phase-3, RIICO Industrial Area, Bhiwadi-901019, INDIA, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260, NDC 77790-022-15.

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 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 I

Navitas, LLC.

Product: NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) IN…
Reason: Potential contamination with Salmonella.
Published: March 4, 2026
Distribution: U.S. Distribution: CA, CO, CT, FL, GA, I…

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FDA Recall United States Terminated 2026 recordClass I

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Product: Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 81009389…
Reason: Undeclared allergen ingredient (Wheat and Sesame)
Published: March 4, 2026
Distribution: Product was distributed to 50 consignees…

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FDA Recall United States Terminated 2026 recordClass I

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Product: Fish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 8100938…
Reason: Undeclared allergen ingredient (Wheat and Sesame)
Published: March 4, 2026
Distribution: Product was distributed to 50 consignees…

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FDA Recall United States Terminated 2026 recordClass I

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Product: Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 8100938…
Reason: Undeclared allergen ingredient (Wheat and Sesame)
Published: March 4, 2026
Distribution: Product was distributed to 50 consignees…

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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 Ongoing 2026 recordClass II

Pure Solutions, Inc.

Product: Pure Factors Professional Nighttime Sleep Formula and Pure F…
Reason: Label declares bovine colostrum but does not declare milk allergen.
Published: February 25, 2026
Distribution: Product was distributed to: AR, FL, CO,…

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FDA Recall United States Ongoing 2026 recordClass I

Lotus Mom Corporation dba Indian Kitchen Mart

Product: Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HAND…
Reason: Potential contamination with leachable lead.
Published: February 25, 2026
Distribution: U.S. Distribution: CA, CO

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FDA Recall United States Ongoing 2026 recordClass II

Lotus Mom Corporation dba Indian Kitchen Mart

Product: Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN IN…
Reason: Potential contamination with leachable lead.
Published: February 25, 2026
Distribution: U.S. Distribution: CA, CO

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Data last updated: September 8, 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.