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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: VT ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 17, 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

fentaNYL 200 mcg/100 mL (2 mcg/mL) ROPivacaine HCl 0.2% 200 mg/100 mL (2 mg/mL) in 0.9% Sodium Chloride , 100 mL bag, Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1108-36

by QuVa Pharma, Inc.

Reason: Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
Published: December 11, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL 2750 mcg/55 mL (50 mcg/mL) 55 mL Syringe, Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1100-50

by QuVa Pharma, Inc.

Reason: Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
Published: December 11, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL 200 mcg/100 mL (2 mcg/mL) ROPivacaine HCl 0.2% 200 mg/100 mL (2 mg/mL) in 0.9% Sodium Chloride 100 mL CADD, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478NDC 70092-1259-75

by QuVa Pharma, Inc.

Reason: Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
Published: December 11, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Regular Strength Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC's 67751-152-01 67751-152-02

by Sanofi-Aventis U.S. LLC

Reason: CGMP Deviations: Presence of NDMA impurity detected in product.
Published: December 11, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Regular Strength Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC 50269-222-25.

by Sanofi-Aventis U.S. LLC

Reason: CGMP Deviations: Presence of NDMA impurity detected in product.
Published: December 11, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Cool Mint Tablets Maximum Strength Zantac 150 mg Sanofi Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC's: 0597-0120-06, 0597-0120-08, 0597-0120-09, 0597-0120-24, 0597-0120-38, 0597-0120-50, 0597-0120-76, 0597-0120-78, 0597-0120-80, 0597-0120-82, 0597-0120-87.

by Sanofi-Aventis U.S. LLC

Reason: CGMP Deviations: Presence of NDMA impurity detected in product.
Published: December 11, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Kettle Cuisine, LLC

Product: Marketside Creamy Cauliflower Parmesan Soup 16 ounce UPC C…
Reason: Soup labeled Creamy Cauliflower Parmesan Soup may contain undeclared fish and wheat
Published: December 11, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lamb Weston Inc

Product: Lamb Weston Grown In Idaho Crispy Hash Brown Dices, packaged…
Reason: Crispy Hash Brown Dices product is recalled because it may contain pieces of hard rubber material.
Published: December 11, 2019
Distribution: distributed in AZ, CA, CO, CT, GA, MA, M…

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FDA Recall United States Terminated Historical recordClass I

Mill Stream Corp.

Product: Sullivan Harbor Farm Smokehouse Refrigerated, Ready-to-Eat,…
Reason: Low water phase salt.
Published: December 11, 2019
Distribution: Multiple states

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FDA Recall Terminated Historical recordClass II

Potassium Phosphate, Monobasic, Crystal, NF, Multi-Compendial, Bulk Pharmaceutical Chemical, packaged in a) 500G glass bottles, product number 3248-01, NDC 10106-3248-1; b) 2.5KG glass bottles, product number 3248-05, NDC 10106-3248-2; c) 12KG pails, product number 3248-07, NDC 10106-3248-3; d) 1KT bottles and drums, product number 3248-X2; e) 1KT bottles and drums, product number 3248-X3; f) 12KG pails, product number 7390-19; Avantor Performance Materials, LLC, 100 Matsonford, Road, Suite 200, Radnor, PA 19087.

by Avantor Performance Materials Inc

Reason: Failed Stability Specifications: Product exceeds compendia and firm's specifications for iron content.
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lidocaine HCl Injection, USP, 2% 100 mg/5 mL (20 mg/mL), Preservative-Free, packaged in 10 x 5 mL Single Dose Vials per carton, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520, NDC 55150-165-05.

by AuroMedics Pharma LLC

Reason: Presence of Foreign Substance: Foreign material found inside the vial.
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Aurobindo Ranitidine Capsules 150 mg, 500 count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-05

by AuroMedics Pharma LLC

Reason: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5mL) 474 mL bottle, Rx only Distributed by: Aurobindo Pharma USA Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India NDC 65862-431-74

by AuroMedics Pharma LLC

Reason: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Aurobindo Ranitidine Capsules 300 mg, 30-count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-145-30

by AuroMedics Pharma LLC

Reason: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Aurobindo Ranitidine Caspules 150 mg, 60-count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-60

by AuroMedics Pharma LLC

Reason: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

DG Health Acid Reducer Ranitidine Tablets 150 mg, 8-count carton, Distributed by: Dolgencorp LLC 100 Mission Ridge Goodletville TN 37072 NDC 55910-092-79

by AuroMedics Pharma LLC

Reason: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AVKARE Ranitidine Tablets, USP 300 mg Rx Only NDC Manufactured for: AvKARE, Inc. Pulaski, TN 38478 a) 250 tablets NDC 42291-725-25; b) 30 tablets NDC 42291-725-30

by AVKARE Inc.

Reason: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AVKARE Ranitidine Tablets, USP 150 mg Rx Only Manufactured for: AvKARE, Inc. Pulaski, TN 38478 Manufactured by: Amneal Pharmaceuticals of NY Hauppauge, NY 11788 a) 1000 tablets NDC 42291-724-10; b) 180 tablets NDC 42291-724-18; c) 60 tablets NDC 42291-724-60

by AVKARE Inc.

Reason: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution, 10 mL per vial, New Vitalis Pharmacy

by New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Reason: Lack of sterility assurance.
Published: December 4, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Amiodarone Hydrochloride Injection, USP, 900 mg per 18 mL (50 mg / mL), 18 mL Multiple Dose Vial, Rx only, Distributed by AuroMedics Pharma LLC E. Windsor, NJ. 08520, Made in India. NDC 55150-182-18

by AuroMedics Pharma LLC

Reason: Crystallization: Presence of visible particulate matter.
Published: December 4, 2019
Distribution: Nationwide

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Data last updated: September 17, 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.