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Recall totals

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

37,497

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,881

Class I recallsReasonable probability of serious health consequences

24,543

Class II recallsTemporary or medically reversible health consequences

2,935

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 2,098 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 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 11, 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	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

FOLIC ACID 10MG/ML W/PRES. (METHYLPARABEN 0.05%, PROPYLPARABEN 0.025% IN NACL, 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

FOLIC ACID 10MG/ML IN NACL (PF), 1ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

ESTRADIOLVAL 3MG/TEST CYP 35MG/ TEST PROP 35MG/ML W/PRES. (BENZYL ETOH 2%), 3ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

EDTA DISODIUM 15% (150MG/ML), 20ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

DMSO 99.9 (PF), In a) 5ML Vials and b) 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

DMPS 50MG/ML (PF), 5ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

DEXPANTHENOL 250MG/ML W/PRES. (BENZALKONIUM CHL 0.01%), 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

DEXPANTHENOL 250MG/ML (PF), In a) 2ML Vials and b) 5ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

CESIUM CHLORIDE 600MG/ML (PF), 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

CALCIUM SODIUM EDTA 300MG/ML (PF), 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX W/METHYL B12/LIDO W/PRES (BENZYL ETOH 2%), B1-100MG, B2-5-PO4-2MG, B3-50MG, B5-2MG, B6-2MG, LIDOCAINE 1%, METHYL B12 1MG/ML, In a) 1ML Vials, b) 5ML Vials, and c) 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX W/CYANO B12 W/PRES., (BENZYL ETOH 2%), B1-100MG, B2-5-PO4-2MG, B3-50MG, B5-2MG, B6-2MG, CYANO B12 1MG/ML, In a) 2ML Vials, b) 5MLVials, c) 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX 50 IN NACL 0.9% W/PRES., (BENZYL ETOH 2%), B1-50MG, B2-5-PO4-5MG, B3-50MG, B5-50MG, B6-50MG/ML, 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX 50 IN NACL 0.9% (PF) B1-50MG, B2-5-PO4-5MG, B3-50MG, B5-50MG, B6-50MG/ML, 2ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX WITHOUT B12 W/PRES (BENZYL ETOH 2%), B1-100MG, B2-5-PO4-2MG, B3-50MG, B5-2MG, B6-2MG/ML, In a) 5ML Vials and b) 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX WITHOUT B12 (PF) IN NACL 0.9%, B1-100MG, B2-5-PO4-2MG, B3-50MG, B5-2MG, B6-2MG/ML, In a) 2ML Vials and b) 5ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX (LIEBERMAN) IN NACL 0.9% (PF), B1-12.5MG, B2-5-PO4-10MG, B3-12.5MG, B5-12.5MG, B6-12.5MG/ML, 2ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX #3 W/PRES (BENZYL ETOH 2%), B1-100MG, B2-5-PO4-2MG, B3-100MG, B5-2MG, B6-2MG/ML, 10ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 16, 2017Historical recordClass II

B-COMPLEX #3 (PF), B1-100MG, B2-2-PO4-2MG, B3-100MG, B5-2MG, B6-2MG/ML, 2ML Vials, MEDAUS PHARMACY

by Medaus, Inc.

Reason: Lack of Assurance of Sterility
Published: July 20, 2016
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 16, 2016Historical recordClass II

Magic Seasoning Blends, LLC

Product: OUTBACK STEAKHOUSE CRAWFISH/CHICKEN/CALAMARI BREADER, NET W…
Reason: There is a potential presence of peanut protein in certain lots of milled flour which was used in custom seasoned flour blends.
Published: July 20, 2016
Distribution: Nationwide

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Data last updated: November 11, 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.