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Recall totals

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

37,327

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,859

Class I recallsReasonable probability of serious health consequences

24,440

Class II recallsTemporary or medically reversible health consequences

2,900

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 2,095 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/imperio-distribution-llc-recalls-beef-jerky-products-produced-without-benefitPublished October 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 26, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

FDA Recall Ongoing2026 recordClass II

0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 100 mL in a Single Dose freeflex bag, Rx only, BD Beckton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417 USA, Distributed by BD, Manufactured by: Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Sale NDC Number: 17271-701-03.

by Fresenius Kabi USA, LLC

Reason: Lack of Assurance of Sterility
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

0.9% Sodium Chloride Injection, USP, 50 mL x60, Becton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417 USA, Distributed by BD, Manufactured by Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Sale NDC Number: 17271-701-02.

by Fresenius Kabi USA, LLC

Reason: Lack of Assurance of Sterility
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

0.9% Sodium Chloride Injection, USP, (4,500 mg per 500 mL) (9 mg per mL) 500 mL in a 500 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 65219-472-05, Unit of Sale NDC Number: 65219-472-20.

by Fresenius Kabi USA, LLC

Reason: Lack of Assurance of Sterility
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

0.9% Sodium Chloride Injection, USP, (2,250 mg per 250 mL) (9 mg per mL) 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 65219-470-05, Unit of Sale NDC Number: 65219-470-30.

by Fresenius Kabi USA, LLC

Reason: Lack of Assurance of Sterility
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

0.9% Sodium Chloride Injection, USP, 0.9% (900 mg per 100 mL) (9 mg per mL) 100 mL in a 100 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 600047, Unit of Use NDC: 65219-468-05, Unit of Sale NDC Number: 65219-468-50.

by Fresenius Kabi USA, LLC

Reason: Lack of Assurance of Sterility
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

0.9% Sodium Chloride Injection, USP 0.9% (450 mg per 50 mL) (9 mg per mL) 50 mL, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 65219-466-05, Unit of Sale NDC Number: 65219-466-60.

by Fresenius Kabi USA, LLC

Reason: Lack of Assurance of Sterility
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg per mL), 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 63323-626-03, Unit of Sale NDC Number: 63323-626-25 (30 bags in 1 case).

by Fresenius Kabi USA, LLC

Reason: Lack of Assurance of Sterility
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Lanreotide Injection, 120 mg/0.5 mL, Box contains 1 Pre-filled syringe, Single dose only, Rx Only, Manufactured by: Pharmathen International, S.A., Rodopi, Greece. Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC 69097-906-67

by Cipla USA, Inc.

Reason: Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Lanreotide Injection, 120 mg*/0.5 mL, Box contains 1 Pre-filled syringe and 1 safety needle, Single dose only, Rx Only, Manufactured by: Pharmathen International, S.A., Rodopi, Greece. Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67

by Cipla USA, Inc.

Reason: Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
Published: April 15, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing2026 recordClass II

Blueroot Health, Inc.

Product: Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, is…
Reason: Contains undeclared egg, soy, and hazelnut
Published: April 15, 2026
Distribution: Alaska, Arizona, California, Colorado, C…

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FDA Recall United States Ongoing2026 recordClass II

Riverence Provisions LLC

Product: Riverence Smoked Trout Dip, net wt. 7oz. Product is perishab…
Reason: Label declares cream cheese but does not declare milk
Published: April 15, 2026
Distribution: Distributed in CA, MA, NJ, NY, OR, TX, U…

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FDA Recall United States TerminatedTerminated: April 28, 20262026 recordClass II

F&S Fresh Foods, Inc.

Product: ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, peri…
Reason: Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.
Published: April 15, 2026
Distribution: distributed in OR

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FDA Recall United States TerminatedTerminated: July 14, 20262026 recordClass II

Zarlengo Italian Ice

Product: Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon…
Reason: Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Published: April 15, 2026
Distribution: IL, IN and TX

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FDA Recall United States TerminatedTerminated: July 14, 20262026 recordClass II

Zarlengo Italian Ice

Product: Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl…
Reason: Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Published: April 15, 2026
Distribution: IL, IN and TX

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FDA Recall United States TerminatedTerminated: July 14, 20262026 recordClass II

Zarlengo Italian Ice

Product: Zarlengo's Chocolate Chocolate Chip Gelato packaged in multi…
Reason: Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Published: April 15, 2026
Distribution: IL, IN and TX

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FDA Recall Ongoing2026 recordClass I

Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further packaged in cartons of 12 x 100 mL IV bags, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad, 382110, India, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1720-3.

by Amneal Pharmaceuticals, LLC

Reason: Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.
Published: April 8, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Prazosin Hydrochloride Capsules, USP, 5mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma LLC, Piscataway, NJ, NDC 70377-068-11.

by Appco Pharma LLC

Reason: cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
Published: April 8, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Prazosin Hydrochloride Capsules, USP, 2mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma LLC, Piscataway, NJ, NDC 70377-067-11.

by Appco Pharma LLC

Reason: cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
Published: April 8, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Prazosin Hydrochloride Capsules, USP, 1mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma LLC, Piscataway, NJ, NDC 70377-066-11.

by Appco Pharma LLC

Reason: cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
Published: April 8, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Artificial Tears Sterile Lubricant Eye Drops (polyvinyl alcohol 0.5%, povidone 0.6%), 0.5 FL OZ (15 mL) bottles; a) LEADER, DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70000-0011-1; b) Good Sense, Distributed By: Perrigo Direct, Inc., Peachtree City, GA 30269, www.PerrigoDirect.com, NDC 50804-110-01; c) Good Neighbor Pharmacy, Distributed By AmerisourceBergen, Conshohocken, PA 19428, NDC 24385-006-05; d) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 09331 7; e) Best Choice, PROUDLY DISTRIBUTED BY: VALU MERCHANDISERS, CO., KANSAS CITY, KS 66106, UPC 0 70038 47008 3; f) Kroger, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202, UPC 0 11110 38600 7; g) P, DISTRIBUTED BY PUBLIX SUPER MARKETS, INC, LAKELAND, FL 33811, UPC 0 41415 00976 9; h) Quality Choice, Distributed by CDMA Inc, Novi, MI NDC 83324-189-14

by K.C. Pharmaceuticals, Inc

Reason: Lack of Assurance of Sterility
Published: April 8, 2026
Distribution: Nationwide

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Data last updated: October 26, 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.