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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 27, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

BevaDex (bevacizumab) 0.06mL Prefilled 32 g (1.25mg/1mg) Syringes, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659 (877) BELLA.

by Bella Pharmaceuticals, Inc.

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

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FDA Recall Terminated Historical recordClass II

Bevacizumab Prefilled 30g and 31 gram 1.25mg/0.05mL Syringes, 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 Terminated Historical recordClass II

Fluorescein Sodium, 5mL 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 Terminated Historical recordClass II

Sodium Bicarbonate 8.4%, 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 Terminated Historical recordClass II

Phenylephrine2.5%/Tropicamide 1% Ophthalmic Solution, 15mL bottle, 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 Terminated Historical recordClass II

Lidocaine Ophthalmic Gel 3.5%, 15mL bottles, 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 Terminated Historical recordClass II

MIC 25/50/50, 30mL 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 Terminated Historical recordClass II

L-Glutamine 100mg, 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 Terminated Historical recordClass II

Magnesium Chloride 200mg, 30m L 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 Terminated Historical recordClass II

Methylcobalamin 10mg, (10mg/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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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

View recall →

Data last updated: September 27, 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.