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Recall totals

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

37,115

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 15, 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 United States Terminated Historical recordClass II

Champlain Chocolate Company

Product: Lake Champlain Chocolates - gift basket- BE MINE; Net Wt. 2l…
Reason: Chocolate may contain plastic pieces
Published: February 10, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Champlain Chocolate Company

Product: "Lake Champlain Chocolates ***NET WT. 9 oz. (255 g)***a sens…
Reason: Chocolate may contain plastic pieces
Published: February 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Ketorolac Tromethamine Injection, USP, 30 mg per mL, packaged in 1 mL Single Dose Vials (NDC 63323-162-00); 25 x 1 mL Single Dose Vials per tray (NDC 63323-162-01); For IM or IV use, Rx only, Fresenius Kabi, Lake Zurich, IL 60047.

by Fresenius Kabi USA, LLC

Reason: Presence of Particulate Matter - found in reserve sample vials at the firm.
Published: February 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Phytonadione Tablets 5mg, 30-count bottle, Rx Only, Manufactured For: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USA NDC 68682-170-30

by Bausch Health Companies, Inc.

Reason: Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.
Published: February 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Mephyton (phytonadione) Tablets 5mg, 100-count bottle, Rx Only, Manufactured for: Valeant Pharmaceuticals North America, LLC Bridgewater, NJ 08807 USA NDC 0187-1704-05

by Bausch Health Companies, Inc.

Reason: Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.
Published: February 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Testosterone Cypionate Injection, USP CIII 200mg/ml FOR INTRAMUSCULAR USE ONLY 1mL Single-dose vial Distributed by: Sun Pharma Ind. Inc, NJ 08512 Manufactured by: Sun Pharma Ind. Ltd., India NDC 62756-015-40

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Incorrect Labeling: Incorrect lot number on secondary packaging
Published: February 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 10.1 fl. oz. (300 ml), Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384. Labeled as Thrifty White Pharmacy Wash-Free Hand Sanitizer. UPC 8 19845 00599 2

by Shane Erickson Inc

Reason: CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Published: February 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 3.4 fl. oz. (100 ml), Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384. Labeled as a) SAFE-GUARD Products International, b) Safe-WAY JEVCO Wash-Free Hand Sanitizer, c) TRACTION CAPITAL, d) United States Census 2020. UPC 8 19845 00598 5

by Shane Erickson Inc

Reason: CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Published: February 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 1.7 fl. oz. (50 ml) bottles, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384, Made in China, ALSO distributed with Custom front labels as follows a) Sadie G. Mays Health & Rehabilitation Center, b) Pacers logo, c) northwood CHURCH, d) ROGERTHEROOFER.com and e) SoFi Stadium Wash-Free Hand Sanitizer. UPC 8 19845 00597 8

by Shane Erickson Inc

Reason: CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Published: February 3, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

EMILIA FOODS SRL

Product: Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Ke…
Reason: Good and Gather Four Cheese Gnocchi may contain foreign material.
Published: February 3, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ceftazidime Sterile Ophthalmic Solution for Injection Preservative Free 11.25mg / 0.5ml (22.5mg/ml) 0.5ml per syringe. KEEP FROZEN UNTIL USE AND PROTECT FROM LIGHT SINGLE USE SYRINGE FOR INTRAOCULAR INJECTION Edge Pharma, LLC is an FDA-registered 503B outsourcing facility. This is a compounded (re-packaged) drug. Not for Resale, Hospital/Office use only. Edge Pharma, LLC 856 Hercules Dr. Colchester, VT 05446 Customer Service (USA) 1-802-992-1178

by Edge Pharma, LLC

Reason: Lack of Assurance of Sterility; the media used to conduct post-compounding sterility testing for the Methotrexate product was expired.
Published: January 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HUMAN CHORIONIC GONADOTROPIN 1,250 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035

by Complete Pharmacy and Medical Solutions, LLC.

Reason: CGMP deviations: Lack of potency testing.
Published: January 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HUMAN CHORIONIC GONADOTROPIN 5,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035

by Complete Pharmacy and Medical Solutions, LLC.

Reason: CGMP deviations: Lack of potency testing.
Published: January 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HUMAN CHORIONIC GONADOTROPIN 6,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035

by Complete Pharmacy and Medical Solutions, LLC.

Reason: CGMP deviations: Lack of potency testing.
Published: January 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HUMAN CHORIONIC GONADOTROPIN 11,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035

by Complete Pharmacy and Medical Solutions, LLC.

Reason: CGMP deviations: Lack of potency testing.
Published: January 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie company Madison, NJ 07940 UPC 3 00236 63410 0, NDC 0023-6634-10.

by Allergan, PLC.

Reason: Labeling: Missing instructions for use insert
Published: January 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100 per carton (10 capsules x 10 blister cards), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC Carton: 68084-446-01; NDC Blister Card: 68084- 446-11

by American Health Packaging

Reason: Failed Dissolution Specifications
Published: January 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Oxycodone Hydrochloride Oral Solution, USP 5 mg/5mL unit dose cups, Rx Only, Genus Lifesciences Inc. NDC 64950-354-05 Case NDC: 64950-354-450(40 unit dose cups) Case NDC 64950-354-55 (50 unit dose cups)

by Genus Lifesciences Inc.

Reason: Presence of Foreign Substance: Particulate matter was found in multiple lots of product.
Published: January 20, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Chlorhexidine Gluconate Oral Rinse USP 0.12%, packaged in a) 15 mL x 30 Unit Dose Cups (30-pack case) NDC 68094-028-61, b) 15 mL x 100 Unit Dose Cups (100-pack case) NDC 68094-028-62, Rx only, Precision Dose, Inc., South Beloit, IL 61080.

by Precision Dose Inc.

Reason: cGMP deviations: The firm was notified of the manufacturer's expanded recall.
Published: January 20, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg, 100 tablets per bottle, Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120, NDC: 29033-056-01

by Nostrum Laboratories Inc

Reason: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
Published: January 20, 2021
Distribution: Nationwide

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Data last updated: September 15, 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.