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Recall totals

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

37,205

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible-0Published October 1, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 1, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

Bupivacaine 0.25% PF, Bupivacaine 0.5% PF, and Bupivacaine 0.75% PF, manufactured by New England Compounding Center, Framingham, MA

by New England Compounding Center

Reason: Lack of Assurance of Sterility
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Betamethasone Sodium Phosphate 6 mg/mL P Injection, Betamethasone Sodium Phosphate 6 mg/mL PF Injection, Betamethasone Sodium Phosphate 8 mg/mL PF Injection, Betamethasone Sodium Phosphate 12 mg/mL PF Injection, manufactured by New England Compounding Center, Framingham, MA

by New England Compounding Center

Reason: Lack of Assurance of Sterility
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6 mg/mL P Injection, manufactured by New England Compounding Center, Framingham, MA

by New England Compounding Center

Reason: Lack of Assurance of Sterility
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Methylprednisolone Acetate 80 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

by New England Compounding Center

Reason: Non-Sterility
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Methylprednisolone Acetate 40 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

by New England Compounding Center

Reason: Non-Sterility
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Methylprednisolone Acetate (PF) 40 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA

by New England Compounding Center

Reason: Non-Sterility
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Methylprednisolone Acetate (PF) 80 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA

by New England Compounding Center

Reason: Non-Sterility
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Synthroid (Levothyroxine Sodium) tablets, 150 mcg (0.15 mg), 90 tablets per bottle, Rx Only, NDC 0074-7069-90; ABBOTT LABORATORIES NORTH CHICAGO, IL 60064 U.S.A.

by Abbott Laboratories

Reason: Labeling: Error on Declared Strength. Product labeled to contain 150 mcg tablets actually contained 75 mcg tablets.
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01

by Hospira Inc.

Reason: Presence of Particulates; may contain glass particles
Published: January 9, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmaceutical Corp, San Juan, PR

by Alara Pharmaceutical Co

Reason: Subpotent; 15 month stability
Published: January 2, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

by Lloyd Inc. of Iowa

Reason: Subpotent; 9-month stability interval
Published: January 2, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thyro-Tab 0.075 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA

by Lloyd Inc. of Iowa

Reason: Subpotent; 9-month stability interval
Published: January 2, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levothroid (levothyroxine sodium tablets, USP), 50 mcg., 100-count bottles, Rx only, NDC 0456-1321-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

by Lloyd Inc. of Iowa

Reason: Subpotent; 9-month stability interval
Published: January 2, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Thyro-Tab 0.050 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

by Lloyd Inc. of Iowa

Reason: Subpotent; 9-month stability interval
Published: January 2, 2013
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lidocaine HCl Injection, USP, 1% (10 mg/mL), 30 mL Single-dose Teartop Vial, packaged in 25-count vials per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045; NDC 0409-4279-02.

by Hospira, Inc.

Reason: Presence of Particulate Matter: Report of a vial containing visible particulate matter embedded in the glass wall which has the potential to dislodge resulting in the presence of particulate matter in the product.
Published: December 26, 2012
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles per carton, NDC 0004-0259-05; b) 120-count capsules per bottle, NDC 0004-0259-51; Made in Ireland; Distributed by: Genentech USA, Inc., South San Francisco, CA 94080.

by Genentech, Inc.

Reason: Short Fill: some bottles contained less than 120-count per labeled claim.
Published: December 26, 2012
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nalbuphine HCl Injection, 20 mg/mL, 10 mL Multiple-dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1467-01

by Hospira, Inc.

Reason: Lack of Assurance of Sterility: Complains of a loose crimp applied to the fliptop vial; and a missing stopper and flip cap were received and therefore sterility cannot be assured.
Published: December 26, 2012
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Choletec - Kit for the Preparation of Technetium Tc 99m Mebrofenin, 10 vials per box, Nonradioactive, Diagnostic Use, For Intravenous Use, Multidose, Rx Only, Manufactured for Bracco Diagnostics Inc. Princeton, NJ 08543, by Hollister-Stier Laboratories LLC, Spokane Washington 99207, NDC 0270-0083-20.

by Bracco Diagnostic Inc

Reason: Presence of Particulate Matter; potential for charcoal particulates
Published: December 26, 2012
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clean & Clear advantage, 3-in-1 foaming wash 8 FL. OZ. (240 mL) bottle, OTC, Distributed in the US by: Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies Inc. Skillman, NJ 08558-9418 NDC 58232-0326-8

by Johnson & Johnson

Reason: Superpotent (Single Ingredient Drug): salicylic acid
Published: December 26, 2012
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Caziant (desogestrel and ethinyl estradiol) Tablets, USP, (Triphasic Regimen), 0.1 mg/0.025 mg, 0.125 mg/0.025 mg, 0.15 mg/0.025 mg, 28-count tablets per dispenser (NDC 52544-959-28), packaged in 3-count Tablet Dispensers per carton (NDC 52544-959-31), Rx only Manufactured by: Watson Laboratories, Inc., Corona, CA 92880; Distributed by: Watson Pharma, Inc., Corona, CA 92880.

by Watson Laboratories Inc

Reason: Impurities/Degradation Products: Out-of-specification results were obtained for a known impurities.
Published: December 26, 2012
Distribution: Nationwide

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Data last updated: October 1, 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.