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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: AR ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 18, 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 United States TerminatedTerminated: February 13, 2026Historical recordClass II

QUEEN BEE GARDENS

Product: Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Inte…
Reason: Product may have small flakes of stainless steel in product.
Published: August 13, 2025
Distribution: Nationwide

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FDA Recall United States CompletedTerminated: September 11, 2026Historical recordClass I

Navarro Pecan Holdings, LLC

Product: FANCY MEDIUM PECAN PIECES 81124 561958 554707 6/13/2025 SDC1…
Reason: Pecans have the potential to be contaminated with Salmonella,
Published: August 13, 2025
Distribution: TX, MN, OK, AR, NJ; UAE, Netherlands, It…

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FDA Recall OngoingHistorical recordClass II

Lorazepam Injection, USP, 2 mg/mL, 25 x 1mL vials/carton, Rx Only, Manufactured by: Hikma Berkeley Heights, NJ 07922, NDC# 0641-6044-25

by Hikma Pharmaceuticals USA Inc.

Reason: Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Sucralfate Tablets, USP 1 gram, packaged in a) 100-count bottles NDC 29033-0003-01, and b) 500-count bottles, NDC 29033-0003-05), Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120.

by Nostrum Laboratories, Inc.

Reason: CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Cinacalcet Tablets 90 mg, 30-count bottles, Rx only, Manufactured by: Strides Pharma Science Ltd. Puducherry, India; Distributed by: Strides Pharma Inc. East Brunswick, NJ 08816, NDC 64380-885-04

by Strides Pharma, Inc.

Reason: Failed Dissolution Specifications.
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , Syringe NDC-60793-702-04

by Pfizer Inc.

Reason: CGMP Deviations; particulates identified during visual inspection
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001. Made in Austria, Carton NDC - 60793-701-10, Syringe NDC - 60793-701-02

by Pfizer Inc.

Reason: CGMP Deviations; particulates identified during visual inspection
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-05.

by FDC Limited

Reason: Defective Container: spike of the cap becomes lodged in the nozzle of the product bottle.
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg, 100 Capsules bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL, 34108, United States, Manufactured by: Lupin Limited, Goa 103 722, INDIA, NDC 68180-755-01.

by Lupin Pharmaceuticals Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 21, 2025Historical recordClass II

NuNaturals Inc

Product: Pure Monk Fruit Sweetener, net wt. 0.71oz. UPC 7 39223 00187…
Reason: Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit Sweetener.
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 21, 2025Historical recordClass II

NuNaturals Inc

Product: Organic Pure Stevia, net wt. 1oz. UPC 7 39223 00204 0. Produ…
Reason: Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
Published: August 6, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pithampur, India. Manufactured for: Ciple USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC# 69097-319-86 (pouch), 69097-319-87 (carton)

by Cipla USA, Inc.

Reason: Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.
Published: July 30, 2025
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 5, 2026Historical recordClass II

clomiPRAMINE Hydrochloride Capsules USP 25 mg, 100 count bottles, 5801 Pelican Bay Boulevard, Suite 500, Naples, Florida 34108, NDC# 68180-492-01

by Lupin Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during retention sample testing at expiry.
Published: July 30, 2025
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass III

Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.

by Imprimis NJOF, LLC

Reason: Sub-Potent Drug: Subpotent assay results during stability testing.
Published: July 30, 2025
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01

by Imprimis NJOF, LLC

Reason: Sub-Potent Drug: Subpotent assay results during stability testing.
Published: July 30, 2025
Distribution: Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Mondelez Global Llc

Product: Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 co…
Reason: Undeclared allergens (Peanut) due to mispackaging
Published: July 30, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States OngoingHistorical recordClass II

Mondelez Global Llc

Product: Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20-…
Reason: Undeclared allergens (Peanut) due to mispackaging
Published: July 30, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States OngoingHistorical recordClass II

Mondelez Global Llc

Product: Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 c…
Reason: Undeclared allergens (Peanut) due to mispackaging
Published: July 30, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States OngoingHistorical recordClass II

Mondelez Global Llc

Product: Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 co…
Reason: Undeclared allergens (Peanut) due to mispackaging
Published: July 30, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: August 18, 2025Historical recordClass II

LEWIS BAKERIES

Product: Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/…
Reason: Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts was put in the Artisan Style 1/2 loaf bags. Bags do not have allergen statement that includes hazelnuts.
Published: July 30, 2025
Distribution: Product was distributed to: TN, KS, AR,…

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Data last updated: October 18, 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.