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Recall totals

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

37,063

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 11, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Ongoing Historical recordClass I

ALPHASTRIP MALE PERFORMANCE ENHANCER, The fastest acting sublingual, Serving Size (1 strip), Distributed by: GALT INT'L

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

The GOAT SUBLINGUAL STRIP, MALE ENHANCEMENT, 2 Pack, Distributed by Hombres LLC, 130 Maccormick Ave, Suite 105, Costa Mesa, A, UPC 6 61631 26363 1.

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

SILVERBACK XXX POWER MALE ENHANCEMENT, 2 fl. oz., UPC 8 700470 032762

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

libigrow RED DRAGON+, Maximum Strength Formula, 2 capsules per box, UPC 7 05105 83073 5.

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural, UPC: N/A.

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Pink Pussycat Honey, net wt: 20gx12 sachets, UPC 7 918750 046557

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Samurai-X Honey 6800, UPC 2 56891 27553 3.

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Flower Power, CBD infused Female Enhancement, 59 ml bottle, UPC 0 678741 351646.

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Weiner Boner Honey, 12g packet, 100% Organic Formula.

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Spanish Fly 22K capsules, 2-count box, UPC 0 664979 979455

by Pyramids Wholesale Inc.

Reason: Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and/or tadalafil.
Published: May 1, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

S.P.Labs, Thyroid, Full Strength, Rx only, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs, Phoenix, AZ 85034, NDC 81305-500-01.

by Specialty Process Labs LLC

Reason: Failed Stability Specifications
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Sterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGULAR (insulin human injection), Insulin Lispro Injection u-100, 10 mL, Use ONLY with Insulins listed on carton, Marketed by: Lilly USA, LLC, Indianapolis, IN 46285. NDC: 0002-0800-01

by Eli Lilly & Company

Reason: CGMP Deviations
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Digoxin Tablets, USP 62.5 mcg (0.0625 mg), 100-count bottles, Rx Only, Manufactured by: Novitium Pharma LLC, 70 Lake Drive, East Windsor, New Jersey 08520, NDC 70954-200-10

by Novitium Pharma LLC

Reason: Failed Impurities/Degradation Specifications
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Vancomycin Hydrochloride for Oral Solution, USP, 250 mg per 5 mL, packaged as (a) 80 mL bottle, NDC 69238-2261-3; (b) 150 mL bottle, NDC 69238-2261-7; (c)300 mL bottle, NDC 69238-2261-5; Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807

by Amneal Pharmaceuticals of New York, LLC

Reason: Superpotent Drug: Due to overfilling of drug powder
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass III

NEXLIZET (bempedoic acid and ezetimibe) tablets, 180 mg/10 mg, 30-count bottle, Rx only, Manufactured for: Esperion Therapeutics, Ann Arbor, MI 48108, NDC 72426-818-03

by Esperion

Reason: Failed dissolution specifications: out-of-specification bempedoic acid dissolution at the 0-month timepoint.
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

S.P Labs, Thyroid, USP, Rx only, For Manufacturing, Processing or Repackaging Use only, Specialty Process Labs, Phoenix, AZ, NDC #'s a) 81305-100-01, b)81305-100-02, c)81305-100-03

by Specialty Process Labs LLC

Reason: Failed Stability Specifications
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Atovaquone Oral Suspension USP, 750 mg per 5 mL sachets, 20 Units x 5 mL cartons, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 50268-086-12.

by AvKARE

Reason: Microbial contamination of a non-sterile product: potential Bacillus cereus contamination.
Published: April 24, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Methocarbamol Injection, USP 1000mg/10mL, (100mg/mL), 10 mL Single-Dose Vial packed 25 vials per carton, Rx Only, Mfd. in India for: Eugia US LLC. E. Windsor, NJ 08520, NDC 55150-223-10

by Eugia US LLC

Reason: Presence of Particulate Matter
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Isotretinoin Capsules, USP 40mg, 30-count 3x10 blister packs per carton, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054. Blister Pack NDC 0591-2436-45, Carton NDC 0591-2436-15

by Teva Pharmaceuticals USA, Inc

Reason: Superpotent Drug: The 3-month stability result for assay was found to be above specification limit
Published: April 17, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14 capsules per bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41

by NATCO Pharma Limited

Reason: CGMP Deviations
Published: April 17, 2024
Distribution: Nationwide

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Data last updated: September 11, 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.