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Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 9, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: April 23, 2018Historical recordClass II

B-Complex, 30 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659,1 (877) BELLA.

by Bella Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 23, 2018Historical recordClass II

Calcium chloride 10%, 10 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.

by Bella Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 23, 2018Historical recordClass II

G.A.C 25/100/250mg, 30 mL Vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.

by Bella Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 23, 2018Historical recordClass II

Mannitol 20%, 10 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.

by Bella Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 23, 2018Historical recordClass II

Methylcobalamin 10mg, (1mg/ml), 30 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.

by Bella Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 23, 2018Historical recordClass II

PF-Glutathione 200mg/ml, 30 mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659 1 (877) BELLA.

by Bella Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 27, 2018Historical recordClass I

Super Panther 7K Capsules 1250 mg blend, a) 1 count blister cards shipped in boxes of 30 (UPC# 6015577513247); and b) 6 count bottles (UPC# 601577513209), Distributed by SX Power CO., Brooklyn, NY

by Chiavna Saffron LLC

Reason: Marketed without an Approved NDA/ANDA;FDA analysis found product to be tainted with sildendafil and tadalafil
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 10, 2018Historical recordClass I

New Kopi Jantan Tradisional Natural Herbs Coffee, packaged in 13 gram red packets, and each box contains 25 packets, Made in Malaysia, USA Distributor: Bestherbscoffee LLC (USA), Email: bestherbscoffee@yahoo.com

by BESTHERBS COFFEE LLC

Reason: Marketed without an approved NDA/ANDA: presence of undeclared desmethyl carbodenafil and undeclared milk.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 14, 2020Historical recordClass II

Ninjacof-A (Acetaminophen 160 mg, Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz. (473 mL), Cotton Candy Flavor, Manufactured for: Centurion Labs, LLC Birmingham, AL 35243 --- NDC 23359-033-16

by Centurion Labs, LLC

Reason: Microbial contamination of Non-sterile Products; potential B. cepacia contamination
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 14, 2020Historical recordClass II

Ninjacof (Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz. (473 mL), Cotton Candy Flavor, Manufactured for: Centurion Labs, LLC Birmingham, AL 35243 --- NDC 23359-032-16

by Centurion Labs, LLC

Reason: Microbial contamination of Non-sterile Products; potential B. cepacia contamination
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 11, 2019Historical recordClass III

Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL (Cherry Flavored), 473 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771 ---- NDC 66689-023-16

by VistaPharm, Inc.

Reason: Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class III controlled substance instead of Class II controlled substance
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 21, 2017Historical recordClass II

Vitamin A&D Ointment (petroleum 93.5%), Skin Protectant, NET Wt. 0.18 OZ (5g), Manufactured for Medline Industries, Inc., Northfield, IL 60093 USA. NDC: 53329-090-16

by Medline Industries Inc

Reason: Labeling Mixup; the individual A&D ointment foil packets are incorrectly labeled as petroleum jelly. The boxes and outer case are correctly labeled as A&D ointment.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 6, 2020Historical recordClass II

Paroxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534, NDC 68382-099-06, UPC 3 6838209906 8

by Zydus Pharmaceuticals USA Inc

Reason: Presence of Foreign tablets/capsules: risperidone Tablets were found in bottle of paroxetine Tablets
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 25, 2018Historical recordClass III

AMLODIPINE BESYLATE TABLET, USP, 10 mg, 1000 count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India, Distributed by: Ascend Laboratories, LLC Montvale, NJ 07645, NDC 67877-199-10

by Ascend Laboratories LLC

Reason: PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet was found co-mingled with 10 mg Amlodipine Besylate tablets in a bottle labeled as Amlodipine Besylate 10 mg.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 14, 2017Historical recordClass II

Wegmans Food Markets, Inc.

Product: Wegmans Assorted Muffins 4-Pack-18 oz. (1 lb. 2 oz.) 510g p…
Reason: 4-pack may contain banana nut muffin containing walnuts, allergen-walnuts not listed on the ingredient label
Published: September 20, 2017
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: April 28, 2020Historical recordClass II

The Harvard Drug Group

Product: Leader Liquid Vitamin D Supplement for Breastfed Infants, 1…
Reason: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 28, 2020Historical recordClass II

The Harvard Drug Group

Product: Leader Liquid Multivitamin Supplement for Infants and Toddle…
Reason: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 28, 2020Historical recordClass II

The Harvard Drug Group

Product: Major Tri-Vita Drops, 1 2/3 oz (50 mL)
Reason: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 28, 2020Historical recordClass II

The Harvard Drug Group

Product: Major Poly-Vita Drops with Iron, 1 2/3 oz (50 mL)
Reason: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published: September 20, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: April 28, 2020Historical recordClass II

The Harvard Drug Group

Product: Major Poly-Vita Drops, 1 2/3 oz (50 mL)
Reason: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard Drug Group dba Rugby Laboratories are jointly initiating a voluntary recall of multiple supplements due to possible product contamination with B. cepacia, which may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
Published: September 20, 2017
Distribution: Nationwide

View recall →

Data last updated: November 9, 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.