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Recall totals

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

37,271

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 20, 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	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall TerminatedTerminated: April 17, 2024Historical recordClass III

Susvimo (ranibizumab injection), 100mg/mL, sold together as a) carton containing One Susvimo single-dose vial and One Susvimo initial fill needle, NDC 50242-078-55; and b) carton labeled as Susvimo Ocular Implant with Insertion Tool Assembly, containing One carrier with implant and One insertion Tool, UDI 81004259001, GTIN 00810042590014, Rx only, Genentech, Inc., A Member of the Roche Group, South San Francisco, CA 94080-4990.

by Genentech Inc

Reason: Defective Delivery System: Commercial implants do not meet the filed specification for the intended use, a few patients have experienced an issue with the implants that renders it non-functioning.
Published: November 9, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 7, 2023Historical recordClass II

Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg, 30-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India; NDC 62756-970-83

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Presence of Foreign Substance
Published: November 9, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 10, 2025Historical recordClass I

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.

by Exela Pharma Sciences LLC

Reason: Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 10, 2025Historical recordClass I

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx only, Manufactured and Distributed by: Exela Pharma Sciences, LLC Lenoir, NC 28645. Carton NDC 51754-5001-5, vial NDC 51754-5001-1

by Exela Pharma Sciences LLC

Reason: Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Quinapril and Hydrochlorothiazide Tablets, USP 20mg/12.5mg, 90 Tablets bottles Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520, Made in India, NDC 65862-162-90

by Aurobindo Pharma USA Inc.

Reason: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 20, 2025Historical recordClass I

Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC 60429-027-10

by Golden State Medical Supply Inc.

Reason: Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 30, 2024Historical recordClass II

Pyridostigmine Bromide Oral Solution, USP 60 mg/5 mL Delivers 5 mL, packaged in 5mL unit-dose cup, Rx only, Dist. by: VistaPharm, NDC 66689-406-01

by VistaPharm, Inc.

Reason: cGMP Deviations: Out of specification for assay of one of the preservative ingredients.
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 13, 2024Historical recordClass II

Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills 99.99% of germs, Green Tea and Aloe, Family Safe, No Gels, Water Based, 24 Hour Germ Protection with Moisturizers for Sensitive Skin, a) 8 oz bottle, b) 32 oz bottle, and c) 1.7 fl oz or 50 mL bottle, Supplier details: Ultra Chem Labs, Ontario, CA, Active Ingredients - Benzalkonium Chloride 0.13% (antimicrobial), ULS 8357 0.33% (antimicrobial shield), NDC 79208-001-50.

by Ultra Chem Labs Corp

Reason: Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 13, 2024Historical recordClass II

Proton Armor, Anti-Microbial Alcohol-Free Foaming Hand Sanitizer, kills 99.99% of germs, Odor Free, Family Safe, No Gels, Water Based, 24 Hour Germ Protection with Moisturizers for Sensitive Skin, a) 8 oz bottle, b) 32 oz bottle and c) 1.7 fl oz or 50 mL bottle, Supplier details: Ultra Chem Labs, Ontario, CA, Active Ingredients - Benzalkonium Chloride 0.13% (antimicrobial), ULS 8357 0.33% (antimicrobial shield), NDC 79208-001-50.

by Ultra Chem Labs Corp

Reason: Chemical Contamination and CGMP Deviations: trace amounts of methanol found in one of the components during the manufacturing process.
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 18, 2024Historical recordClass II

Fondaparinux Sodium Injection, USP, 7.5 mg per 0.6 mL, Single Dose, Prefilled Syringe, Distributed by: AuroMedics Pharma LLC 279 Princeton-Hightstown Rd. E. Windsor, NJ 08520. Made in India. NDC 55150-232-10 (carton)NDC 55150-232-00 (syringe)

by AuroMedics Pharma LLC

Reason: Subpotent Drug: Out of specification for assay
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 5, 2024Historical recordClass II

Secrets Of The Tribe

Product: Indian Gooseberry Alcohol-Free Extract, 2 oz. glass bottle,…
Reason: Product has elevated level of lead.
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 5, 2024Historical recordClass II

Secrets Of The Tribe

Product: Amla Alcohol-Free Extract, 2 oz. glass bottle, UPC 041979376…
Reason: Product has elevated level of lead.
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE, USP - 900 mg, WATER FOR INJECTION, USP - qs, 1000mL Bag, 12 PK, Rx Only, Fresenius Medical Care North America, Waltham, MA 02451, NDC 49230-300-10

by Fresenius Medical Care Holdings, Inc.

Reason: Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 25, 2023Historical recordClass III

NDC 0363-6171-09 Walgreens Sinus Pressure, Pain & Cough ACETAMINOPHEN/ PAIN RELIEVER DEXTROMETHORPHAN HBr/ COUGH SUPPRESSANT GUAIFENESIN/ EXPECTORANT PHENYLEPHRINE HCl/ NASAL DECONGESTANT Maximum Strength Decongestant Free DISTRIBUTED BY: WALGREENS CO. 200 WILMOT RD., DEERFIELD, IL 60015 walgreens.com

by LNK International, Inc.

Reason: Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Acyclovir Sodium Injection, 500mg/10mL (50mg/mL), 10 mL Single Dose Vial, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520; Made in India, NDC 55150-154-10.

by AuroMedics Pharma LLC

Reason: Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 19, 2025Historical recordClass II

Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA, NDC 51407-322-30

by Golden State Medical Supply Inc.

Reason: Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 19, 2025Historical recordClass II

Rifampin Capsules, USP, 300 mg, packaged in a) 30-count bottle (NDC 51407-323-30), b) 60-count bottle (NDC 51407-323-60), c) 100-count bottle (NDC 51407-323-01), Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA.

by Golden State Medical Supply Inc.

Reason: Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Flunisolide Nasal Solution, USP 0.025%, 25 mL bottles, Rx only, Manufactured for: Ingenus Pharmaceuticals, LLC Orlando, FL 32839-6408; NDC 50742-317-25 UPC 3 50742 31725 7

by Ingenus Pharmaceuticals Llc

Reason: Out of specification for related substances (impurities).
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 28, 2022Historical recordClass II

D. F. Stauffer Biscuit Co, Inc.

Product: White frosted animal cookies with multi-colored non-pareils…
Reason: Potential contamination with foreign material (metal).
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: May 11, 2023Historical recordClass II

Eden Foods, Inc

Product: Eden Organic Apple Juice in 32floz., 64floz., and 1.82L size…
Reason: culling not performed to remove rotted apples, excessive levels of patulin found in 1 lot
Published: October 19, 2022
Distribution: Nationwide

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Data last updated: October 20, 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.