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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

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

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Source: FDA and USDA public dataLast updated November 8, 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

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

FDA Recall TerminatedTerminated: September 17, 2022Historical recordClass III

QUIK-CARE Aerosol Foam Hand Sanitizer (62.5% Ethyl Alcohol), packaged in 7 oz cans, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102-1390 USA, NDC 47593-490-82

by Ecolab Inc

Reason: Incorrect/undeclared excipients: Hand sanitizer was made using the wrong alcohol raw material.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 28, 2022Historical recordClass III

Myorisan (isotretinoin capsules, USP), 40 mg, packaged in cartons of 30 Capsules containing 3 x 10 Prescription Packs, Rx Only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forest, IL 60045, NDC 61748-304-13

by Akorn Inc

Reason: Labeling: Label mix-up: Product secondary carton erroneously states 40mg instead of 30 mg, primary carton is label correctly.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 27, 2025Historical recordClass III

Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented), a) 15 gram (NDC 52565-019-15) and b) 50 gram (NDC 52565-019-51) tubed, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 06310

by Teligent Pharma, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 8, 2021Historical recordClass II

Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended-Release Tablets, USP, Allergy & Congestion, 20-count box.Distributed by: Walgreen Co. 200 Wilmore Rd. Deerfield, IL 40015. Made in India UPC 3 11917 19453 0

by Sun Pharmaceutical Industries, Inc.

Reason: Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation Specifications: elevated substance results that were reported above or near the specification limit
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 8, 2021Historical recordClass II

Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg/ Extended-Release Tablets, USP, Allergy & Congestion, 30-count box. Distributed by: Walgreen Co. 200 Wilmore Rd. Deerfield, IL 40015. Made in India. UPC 3 11917 19454 7

by Sun Pharmaceutical Industries, Inc.

Reason: Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation Specifications: elevated substance results that were reported above or near the specification limit
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 8, 2021Historical recordClass II

Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended Release Tablets, USP, 20-count box, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895. Made in India. UPC 0 50428 43023 1

by Sun Pharmaceutical Industries, Inc.

Reason: Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation Specifications: elevated substance results that were reported above or near the specification limit
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 8, 2021Historical recordClass II

Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended Release Tablets, USP, 30-count box, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895. Made in India. UPC 0 50428 39131 0

by Sun Pharmaceutical Industries, Inc.

Reason: Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation Specifications: elevated substance results that were reported above or near the specification limit
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: December 27, 2019Historical recordClass II

APS BioGroup, Inc

Product: Immulox, UPC 1 82863 000064 6. Immune Balance Polypeptide Su…
Reason: The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: December 27, 2019Historical recordClass II

APS BioGroup, Inc

Product: DPS Throat Spray, UPC 8 55602 00021 3. Colostrum Immune Conc…
Reason: The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: December 27, 2019Historical recordClass II

APS BioGroup, Inc

Product: Viralox, UPC 8 63784 00015 0. Immune Balancing Ploypeptide O…
Reason: The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: December 27, 2019Historical recordClass II

APS BioGroup, Inc

Product: Immuno PRP Spray, UPC 8 12527 01176 2. Colostrum Polypeptide…
Reason: The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 25, 2019Historical recordClass II

Gertrude Hawk Brands dba Gertrude Hawk Chocolates

Product: R.H. Macy & Co. Milk Chocolate Butter Almond Toffee, 6 oz.…
Reason: Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 25, 2019Historical recordClass II

Gertrude Hawk Brands dba Gertrude Hawk Chocolates

Product: R.H. Macy & Co. Dark Chocolate Sea Salt Caramels, 7 oz. 1 u…
Reason: Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 25, 2019Historical recordClass II

Gertrude Hawk Brands dba Gertrude Hawk Chocolates

Product: R.H. Macy & Co. Milk Chocolate Covered Pecan Caramel Cluster…
Reason: Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 25, 2019Historical recordClass II

Gertrude Hawk Brands dba Gertrude Hawk Chocolates

Product: R.H. Macy & Co. Milk Chocolate Covered Peanut Butter Pretzel…
Reason: Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.
Published: June 26, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 21, 2024Historical recordClass II

Senna (sennosides 8.8 mg) Syrup 8 fl oz. (236 mL) bottles, Distributed by Geritrex, LLC 40 Commercial Avenue Middletown, NY 10941, NDC 54162-007-08

by Geritrex, LLC

Reason: Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported
Published: June 19, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 21, 2024Historical recordClass II

Senna (sennosides 8.8 mg) Syrup, 8 fl oz. (237 mL) bottles, Rij Pharmaceuticals Corporation 40 Commercial Avenue, Middletown, NY 10941, NDC 53807-556-08

by Geritrex, LLC

Reason: Failed Impurities/Degradation Specifications: Atypical odor and unpleasant taste was reported
Published: June 19, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2020Historical recordClass II

Sevoflurane, USP Inhalation Anesthetic 250 mL bottles, Rx only, Manufactured for Baxter Healthcare Corporation Deerfield, IL 60015 USA, NDC 10019-651-64

by Baxter Healthcare Corporation

Reason: Failed Stability Specifications
Published: June 19, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 15, 2020Historical recordClass II

Sn-Pyrophosphate Kit, 11.9 mg sodium pyrophosphate, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.

by Synthetopes Inc

Reason: Lack of Processing Controls.
Published: June 19, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 15, 2020Historical recordClass II

Sn-Tetrofosmin Kit 5.0 mL, Thaw and Vent before use, Not for Direct Injection, Store Frozen, Synthetopes, Inc.

by Synthetopes Inc

Reason: Lack of Processing Controls.
Published: June 19, 2019
Distribution: Nationwide

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Data last updated: November 8, 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.