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Recall totals

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

37,061

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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 10, 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 United States Terminated Historical recordClass II

QUEEN BEE GARDENS

Product: Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended u…
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 Terminated Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Ongoing Historical 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 Completed Historical 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 Terminated Historical 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 Terminated Historical 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 United States Terminated Historical recordClass I

SHEEHAN BROTHERS VENDING

Product: Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw,…
Reason: Undeclared sesame
Published: August 6, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

SHEEHAN BROTHERS VENDING

Product: Sheehan Brothers Vending Chili Cheese Coney, 4.3 oz (120g),…
Reason: Undeclared sesame
Published: August 6, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

SHEEHAN BROTHERS VENDING

Product: Sheehan Brothers Vending Pepperoni Pizza Mini Sub, 4.8 oz (1…
Reason: Undeclared sesame
Published: August 6, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

SHEEHAN BROTHERS VENDING

Product: Sheehan Brothers Vending Italian Mini Sub, 6.1 oz (174g), in…
Reason: Undeclared sesame
Published: August 6, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

SHEEHAN BROTHERS VENDING

Product: Sheehan Brothers Vending Spicy Chicken Sandwich, 6.5 oz (184…
Reason: Undeclared sesame
Published: August 6, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

SHEEHAN BROTHERS VENDING

Product: Sheehan Brothers Vending Cheeseburger, 4.7 oz (132g), indivi…
Reason: Undeclared sesame
Published: August 6, 2025
Distribution: Multiple states

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FDA Recall Ongoing Historical 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 Ongoing Historical recordClass II

BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations; potential temperature excursions due to transit delays
Published: July 30, 2025
Distribution: Within the U.S - OH, VA, FL.

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FDA Recall Ongoing Historical recordClass II

EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-880-02.

by Mckesson Medical-Surgical Inc. Corporate Office

Reason: CGMP Deviations; potential temperature excursions due to transit delays
Published: July 30, 2025
Distribution: Within the U.S - OH, VA, FL.

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Data last updated: September 10, 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.