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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,326
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,859
Class I recallsReasonable probability of serious health consequences
24,440
Class II recallsTemporary or medically reversible health consequences
2,900
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 2,095 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/winco-foods-llc-issues-allergy-alert-undeclared-sesame-hoagie-rollsPublished October 22, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2

Showing 6,321–6,340 of 19,481 recalls

FDA Recall United States TerminatedTerminated: February 16, 2022Historical recordClass I

DREAM POPS

Product
100% Plant-Based Dream Pops Birthday Cake Bites UPC 85409700…
Reason
Undeclared allergen; milk
Published
January 19, 2022
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: February 16, 2022Historical recordClass I

DREAM POPS

Product
100% Plant-Based Dream Pops Berry Dreams Bites UPC 854097008…
Reason
Undeclared allergen; milk
Published
January 19, 2022
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 16, 2022Historical recordClass I

DREAM POPS

Product
100% Plant-Based Dream Pops Vanilla Sky Bites UPC 8540970082…
Reason
Undeclared allergen; milk
Published
January 19, 2022
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: October 27, 2022Historical recordClass I

Joseph Seviroli Inc.

Product
Aplenty Rotini with Plant based Bolognese Meal Kit 24oz
Reason
May contain undeclared milk
Published
January 19, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 6, 2023Historical recordClass II

Pregabalin Capsules, 50 mg, 100 count bottle, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Survey No. 259/15 Dadra-396 191, (U.T. of D & NH), India, NDC 47335-687-88.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Tablet/Capsule Specifications: Out of Specification results for particle Size Distribution and Bulk Density of the Active Pharmaceutical Ingredient.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 13, 2023Historical recordClass II

Cefixime Capsules, 400 mg, 50-count bottles, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ, NDC 67877-584-50

by Ascend Laboratories, LLC

Reason
Failed impurities/degradation specifications
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

GoodSense Aller.Ease, Fexofenadine hydrochloride 24 HR, 180 mg tablets, 30 count bottle, Made in the Czech Republic, Distributed by Perrigo Allergan MI., 49010, UPC 3 0113 0571 39 3; NDC 0113-0571-30,

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

CVS Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, 30 count bottle, NDC 69842-698-39, UPC 0 50428 62564 4

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

KIRKLAND ALLER-FEX, Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24HR, 180 count bottle, Made in the Czech Republic, Packaged by Perrigo 515 Eastern Ave., Allegan, MI 49010, For Costco Wholesale Corporation. P.O. Box 34535 Seattle, WA 98124-1535, NDC 63981-571-48, UPC 0 96619 98776 4

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

amazon basic+care, Allergy Fexofenadine Hydrochloride Tablets, 60 mg/Antihistamine, 12HR, 100 count bottle, Made in the Czech Republic, Distributed by: Amazon.com services LLC 410 Terry Avenue N., Seattle WA 98109, NDC 72288-425-78 UPC 3 70030 14536 2

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

Wal-Fex Fexofenadine Hydrochloride tablets, 60mg/antihistamine, 12HR, 24 count bottle, Distributed by Walgreen Co. 200 Wilmot Rd Deerfield IL 60015, Made in the Czech Republic, NDC 0363-0903-62 UPC 3 11917 18625 2

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

Wal-Fex Fexofenadine Hydrochloride tablets, 180mg/antihistamine, 24HR, packaged as a) 5 count bottle, NDC 0363-0600-13,UPC 3 11917 12267 0, b)30 count bottle, NDC 0363-0600-39 UPC 3 11917 16172 3 c) 90 count bottle, NDC 0363-0600-75 UPC 3 11917 12271 7 ; Distributed by Walgreen Co. 200 Wilmot Rd Deerfield IL 60015, Made in the Czech Republic,

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

up&up allergy relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/antihistamine, packaged as a) 15 count bottle, NDC 11673-571-22 UPC 3 70030 62303 7; b) 30 count bottle, NDC 11673-571-39 UPC 3 70030 62301 3; Distributed by Target Corp., Mpls., MN 55403, Made in the Czech Republic,

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

TopCare Allergy Relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, packaged as a) 5 count bottle, NDC 36800-319-13 UPC 0 36800 33277-5 b) 15 count bottle, NDC 36800-319-22 UPC 0 36800 33278 2; c) 45 count bottle, NDC 36800-319-95 UPC 0 36800 33280-5; d) 90 count bottle, NDC 36800-319-75 UPC 0 36800 33282 9; Distributed Topco Associates LC, Elk Grove Village, IL 60007, Made in the Czech Republic,

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

TopCare Allergy Relief, Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 12 count bottle, Distributed Topco Associates LC, Elk Grove Village, IL 60007, Made in the Czech Republic, NDC 36800-954-53 UPC 0 36800 33284 3

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, packaged as a) 30 count bottle, NDC 11822-0571-2 UPC 0 11822 99908 3; b) 150 count bottle, NDC 11822-0571-5 UPC 0 11822 85411 5; Made in the Czech Republic, Distributed by Rite Aid 30 Hunter Lane Camp Hill PA 17011

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 24 count bottle, Made in the Czech Republic, Distributed by Rite Aid 30 Hunter Lane Camp Hill PA 17011 NDC 11822-0425-0 UPC 0 11822 85410 8

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

Perrigo Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 100 count bottle, Made in the Czech Republic, Distributed by Perrigo Allergan, MI 49010 NDC 45802-425-78 UPC 3 45802 425 78 2

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

Perrigo Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, 100 count bottle, Made in the Czech Republic, Distributed by Perrigo Allergan, MI 49010 NDC 45802-571-78 UPC 3 45802 571 78 6

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: November 8, 2022Historical recordClass II

allergyrelief, Fexofenadine Hydrochloride tablets, 24HR, 1800mg Antihistamine, packaged as a) 15 count bottle, NDC 56062-571-22 UPC 0 41415 38973 1; b) 45 count bottle, NDC 56062-571-95 UPC 0 41415 38773 7; Distributed by PubliX SUpermarket Inc 3300 Publix Corporate Parkway Lakeland, FL 33811, Made in the Czech Republic

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

View recall →

Data last updated:

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.

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