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Recall totals

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

37,118

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 18, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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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FDA Recall Terminated Historical recordClass II

Sn-DTPA Kit 10 mg, DTPA, 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 Terminated Historical recordClass II

Sn-d, l-Exametazime (Sn-d,l-HMPAO), Not for Direct Injection, Store Below 25 C, Synthetopes, Inc.

by Synthetopes Inc

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

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FDA Recall Terminated Historical recordClass II

Sulfur Colloid Reaction Vial 1.0 mL, Thaw 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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FDA Recall Terminated Historical recordClass II

Sn-Mertiatide Kit,1 milligram betiatide, 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 Terminated Historical recordClass II

Sn-DMSA solution, Store Frozen, Not for Direct Injection, Synthetopes, Inc.

by Synthetopes Inc

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

View recall →

Data last updated: September 18, 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.