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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 16, 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

Phentermine HCL Blue/White Capsules, 37.5 mg, 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: KVK-Tech., Inc Newtown, PA 18940; NDC 10702-0029-10

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Phentermine HCL Blue/Clear capsules, 30mg, packaged in a) 10-count bags (NDC 10702-0028-10), b) 28-count bags (NDC 10702-0028-10) and c) 56-count bags (NDC 10702-0028-10), Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by KVK-Tech Newtown, PA 18940; NDC 10702-0028-10

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phentermine HCL Yellow Caps 30mg, packaged in 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: Tagi Pharma, South Beloit, IL 61080; NDC 51224-0202-70

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phentermine HCL GrayYellow capsules, 15mg, packaged in a) 28-count bags and b) 56-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: Tagi Pharma, South Beloit, IL 61080; NDC 51224-0203-70

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phentermine 15mg grey/Yellow Capsules, 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: Sunrise Pharm., Rahway NJ, 07065; NDC 11534-0157-03

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phentermine HCL Gray/Yellow capsules, 15mg, 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123 Manufactured by Kvk-Tech, NDC 10702-0026-10

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phendimetrazine Brown/Clear Capsules, 105 mg, 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Virtus Pharm., LLC Newtown, PA 18940; NDC 69543-0409-11

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phendimetrazine Yellow Tabs 35mg, packaged in a) 10-count bags (NDC 69543-0410-11) and b) 28-count bags (NDC 69543-0410-11), and c) 56-count bags (NDC 69543-0410-11) Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Virtus Pharm, LLC.

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Phendimetrazine Yellow Tabs 35mg, 28-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, MFG: KVK-Tech, Newtown, PA 18940, NDC 0702-0077-10

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Topiramate 25mg Tabs White/round tablets, 10-count bags, Distributed by: Calvin Scott & Co., Inc. Alb., MN 87123, Mfg: Sun Pharm., Inc. Cranbury, NJ 08512, NDC 47335-0707-13

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thyroid Neutral Tabs 2 gr, 28-count tablets, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, MN 87123, Manufactured by RLC, Cave Creek, AZ 85331 Labs, NDC 64727-3308-02

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thyroid 1 Gr tablets, 28-count bags, Rx Only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by RLC Labs Cave Creek, AZ 85331, NDC 64727-3300-01

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thyroid 1 Grain Tablets, 28-count bags, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by RLC Labs, Cave Creek, AZ 85331, NDC 64727-3300-02

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Hydrochlorothiazide 50mg tablets, 14-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Accord Healthcare, Inc., Durham NC 27703; NDC 16729-0184-17

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Hydrochlorothiazide (HCTZ) Orange Tabs 25mg, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123 Manufactured by Unichem Pharmaceuticals, NDC 29300-0128-10

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Hydrochlorothiazide 25mg tablets, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Mfg: Accord Healthcare, Inc, Durham, NC 27703, NDC 16729-0183-17

by Calvin Scott & Company, Inc.

Reason: CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Prednisone Tablets, USP 2.5 mg, 100 tablets, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, Manufactured by: Tianjin Tianyao Pharmaceuticals Co., Ltd No. 221 Huanghai Road, Tianjin Economical-Technological Development Area, Tianjin, China 300457 NDC 0527-2931-37

by Lannett Company, Inc.

Reason: Labeling: Label Mix Up: bottle labeled to contain Prednisone Tablets, USP 2.5 mg actually contained Prednisone Tablets, USP 10 mg
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Elitek (rasburicase) for injection, 7.5 mg vial, Rx Only Mfd. by Sanofi - Aventis U. S. LLC Bridgewater, NJ, 08807, NDC 0024-5151-75

by Sanofi-Aventis U.S. LLC

Reason: Failed Stability Specifications: Out of Specification result for enzyme activity levels noted during routine stability testing.
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

STIMATE (desmopressin acetate) Nasal Spray1.5 mg/mL, 2.5 mL glass vial with spray cap, Rx only, Manufactured for: CSL Behring LLC, King of Prussia, PA 19406-0901; By: Ferring GmbH, Kiel, Germany, NDC 0053-6871-00

by Ferring Pharmaceuticals Inc

Reason: Superpotent Drug
Published: August 26, 2020
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Desmopressin Acetate Nasal Spray 10 mcg/0.1 mL, 5mL glass vial with spray cap, Rx only, Manufactured for: AMRING PHARMACEUTICALS INC., Berwyn, PA 19312, NDC 69918-501-05

by Ferring Pharmaceuticals Inc

Reason: Superpotent Drug
Published: August 26, 2020
Distribution: Nationwide

View recall →

Data last updated: September 16, 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.