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

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Source: FDA and USDA public dataLast updated September 22, 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

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

Hydroxocobalamin 10 mg/mL Injection (ALT) Solution, 30 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

View recall →

FDA Recall Terminated Historical recordClass II

Prostaglandin 20 mcg/mL/Procaine 0.1% Injection, packaged in a) 2.5mL and b)10 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205 (509) 343-6252

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

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FDA Recall Terminated Historical recordClass II

Hydroxyprogesterone Caproate 250 mg/mL Sesame Oil Injection, 5 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

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FDA Recall Terminated Historical recordClass II

Testosterone Cyp/Estradiol Cyp 50 mg/2.5 mg/mL Injection, 3mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate 100 mg/mLOil Injection Injection, 12 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate 200 mg/mL Ethyl Oleate Injection, packaged in a) 7.2 mL. b) 9.6 mL, c) 10.8mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252.

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate 200 mg/mL Sesame Oil Injection, packaged in a) 9 mL, b) 12 mL vials, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343- 6252

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

View recall →

FDA Recall Terminated Historical recordClass II

Testosterone Cypionate 150 mg/mL Sesame Oil Injection, 12 mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343- 6252.

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

View recall →

FDA Recall Terminated Historical recordClass II

Testosterone Cypionate 100 mg/mL Sesame Oil Injection, 12mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252

by First Pharma Associates LLC dba Riverpoint Pharmacy

Reason: Lack of Assurance of Sterility.
Published: July 17, 2019
Distribution: ID, WA only

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FDA Recall Terminated Historical recordClass II

Anastrozole Tablets, USP, 1 mg, a) 30-count (NDC 68001-155-04) and 1000-count (NDC 68001-155-08) bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories

by American Health Packaging

Reason: GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP. 50 mg. NDC# 0904-6390-61. Rx only. 100 count Unit Dose Cartons. Manufactured by Major Pharmaceuticals 17177 N. Laurel Park Drive Suite 233, Livonia, MI 48152.

by MAJOR PHARMACEUTICALS

Reason: CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium, 100 mg tablets, 90 count bottle, NDC 60429-318-90

by Golden State Medical Supply Inc.

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium, 50 mg tablets, 1000 count bottle, NDC 60429-317-10

by Golden State Medical Supply Inc.

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium, 50 mg tablets, 90 count bottle, NDC 60429-317-90

by Golden State Medical Supply Inc.

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium, 50 mg tablets, 30 count bottle, NDC 60429-317-30

by Golden State Medical Supply Inc.

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium andHydrochlorothiazide Tablets 100 mg/25 mg 90 tablets, USP Rx Only, Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-052-10

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/12.5 mg 90 Tablets, USP Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-051-10

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg 90 Tablets, USP Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-050-10

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets 50 mg 1000 Tablets, USP Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-045-44

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP 50 mg 90 tablets Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-045-10

by Macleods Pharma Usa Inc

Reason: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published: July 17, 2019
Distribution: Nationwide

View recall →

Data last updated: September 22, 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.