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Recall totals

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

37,135

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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

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Source: FDA and USDA public dataLast updated September 23, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit contains 2 Epi Safe Administration Kit (8600-01101) and 1 Epi Safe Training Kit (8600-01102), Rx Only. Distributed by Sarnova HC, LLC's family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc., Emergency Medical Producs, Inc. & Tri-anim Health Services, Inc. 5000 Tuttle Crossing Blvd, Dublin, OH 43016

by Bound Tree Medical, LLC

Reason: Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine within kit 8600-01100 expired on December 2018, but the outer kit label has an expiration date of January 2020. In addition, device component (syringe) may lack 510(k) clearance.
Published: January 23, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cefdinir for Oral Suspension USP, 250mg/5mL, packaged in a) 60mL (NDC 68180-723-20), b)100mL (NDC 68180-723-10), Rx Only, Manufactured for: Lupin Pharmaceuticals Inc. Baltimore, MD 21202; Manufactured by: Lupin Limited Mandideep 462 046 INDIA

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: Product complaints received indicating reconstituted suspension was observed to be thick.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cefdinir for Oral Suspension USP, 125mg/5mL, packaged in a) 60mL (NDC 68180-722-20), b)100mL (NDC 68180-722-10), Rx Only, Manufactured for: Lupin Pharmaceuticals Inc. Baltimore, MD 21202; Manufactured by: Lupin Limited Mandideep 462 046 INDIA

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: Product complaints received indicating reconstituted suspension was observed to be thick.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to 20 mL Lyophilized, 10 x 20 mg vials, Rx Only, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway Halol-389 350, Gujarat, India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 NDC: 47335-932-40 [vial] 47335-932-44 [carton]

by Sun Pharmaceutical Industries, Inc.

Reason: Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Vecuronium Bromide for Injection 10 mg, 1mg/mL when reconstituted to 10 mL Lyophilized, 10 x 10 mg vials, Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway Halol-389 350, Gujarat, India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 NDC 47335-931-40 [vial] NDC 47335-931-44 [carton]

by Sun Pharmaceutical Industries, Inc.

Reason: Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Ceftriaxone for Injection USP, 2 g, packaged in 10 Single Use Vials (NDC 68180-644-01) per box, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-644-10.

by Lupin Pharmaceuticals Inc.

Reason: Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Ceftriaxone for Injection USP, 1 g, packaged in a) one Single Use Vial (NDC 68180-633-01) and b) 10 Single Use Vials per box (NDC 68180-633-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep 462 046 INDIA.

by Lupin Pharmaceuticals Inc.

Reason: Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Ceftriaxone for Injection USP, 500 mg, packaged in a) one Single Use Vial (NDC 68180-622-01) and b) 10 Single Use Vials per box (NDC 68180-622-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep 462 046 INDIA.

by Lupin Pharmaceuticals Inc.

Reason: Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Ceftriaxone for Injection USP, 250 mg, packaged in a) one Single Use Vial (NDC 68180-611-01) and b) 10 Single Use Vials per box (NDC 68180-611-10); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep 462 046 INDIA.

by Lupin Pharmaceuticals Inc.

Reason: Presence of Particulate Matter: Product complaints received of grey flecks, identified as shredded rubber particulate matter from the stopper observed in reconstituted vials.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials, Rx only, Mfd by: Emcure Pharmaceuticals Ltd., Hinjawadi, Pune, India Mfg. for : Heritage Pharmaceuticals Inc. NDC 23155-0216-31

by Heritage Pharmaceuticals, Inc.

Reason: Lack of Assurance of Sterility: complaints received about dried powder on the outside of bottle
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5% Dextrose, 2000 mL UltraBag container bag, Rx only; Baxter Healthcare Corporation, Deerfield, IL 60015; Product Code 5B9766, NDC 0941-0424-52.

by Baxter Healthcare Corporation

Reason: Lack of Assurance of Sterility: Confirmed customer complaints for leaks on the tubing.
Published: January 16, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nitrofurantoin Oral Suspension, USP, 25mg/5mL, 230 mL bottle, Rx only, Manufactured by: Novel Laboratories, Inc., Somerset, NJ 08873; Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, NDC 43386-450-11.

by LUPIN SOMERSET

Reason: Subpotent Drug: Expansion of June 2018 recall of lots S700065 and S700619 due to below specification results for assay.
Published: January 9, 2019
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Apio, Inc.

Product: Eat Smart Salad Shake Ups - Tropical Lime/Lime Tropicale 5.…
Reason: Canadian Food Inspection Agency notified firm of positive finding Listeria Monocytogenes in several varieties of Eat Smart Single-Serve Salad Shake Ups.
Published: January 2, 2019
Distribution: Arizona, California, Colorado, Florida,…

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FDA Recall United States Terminated Historical recordClass I

Apio, Inc.

Product: Eat Smart Salad Shake Ups - Sweet Kale/Chou Frise Doux: 5.5…
Reason: Canadian Food Inspection Agency notified firm of positive finding Listeria Monocytogenes in several varieties of Eat Smart Single-Serve Salad Shake Ups.
Published: January 2, 2019
Distribution: Arizona, California, Colorado, Florida,…

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FDA Recall United States Terminated Historical recordClass I

Apio, Inc.

Product: Eat Smart Salad Shake Ups - Raspberry Acai/Framboises ET: 5…
Reason: Canadian Food Inspection Agency notified firm of positive finding Listeria Monocytogenes in several varieties of Eat Smart Single-Serve Salad Shake Ups.
Published: January 2, 2019
Distribution: Arizona, California, Colorado, Florida,…

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FDA Recall United States Terminated Historical recordClass I

Apio, Inc.

Product: Eat Smart Salad Shake Ups - Avocado Ranch/Ranch et Avocats:…
Reason: Canadian Food Inspection Agency notified firm of positive finding Listeria Monocytogenes in several varieties of Eat Smart Single-Serve Salad Shake Ups.
Published: January 2, 2019
Distribution: Arizona, California, Colorado, Florida,…

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FDA Recall United States Terminated Historical recordClass I

Apio, Inc.

Product: Eat Smart Salad Shake Ups - Asian Sesame/Sesame Asiatique;…
Reason: Canadian Food Inspection Agency notified firm of positive finding Listeria Monocytogenes in several varieties of Eat Smart Single-Serve Salad Shake Ups.
Published: January 2, 2019
Distribution: Arizona, California, Colorado, Florida,…

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FDA Recall Terminated Historical recordClass III

Absorica (Isotretinoin) Capsules 30 mg USP, 30 capsules (3x10 Prescription Packs) Rx only, Manufactured by: Galephar Pharmaceutical Research Inc. Humacao, PR 00792, Distributed by: Sun Pharmaceutical Industries Inc. Cranbury, NJ 08512, UPC 310631117313, NDC 10631-117-31 (carton) NDC10631-117-69 (prescription pack)

by Sun Pharmaceutical Industries, Inc.

Reason: Subpotent Drug: Isotretinoin content results were lower than the specification limit obtained during routing product monitoring.
Published: December 26, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Nevirapine Extended Release Tablets, 400 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd. Verna Goa, India, Manufactured for: Cipla USA Inc. 9100 S Dadeland Blvd., Suite 1500 Miami, FL 33156, NDC 69097-403-02

by Cipla Limited

Reason: Failed Dissolution Specifications.
Published: December 26, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%), 30 ML bottle, Manufactured and Distributed by: Results RNA, LLC, 1272 S 1380 W., Orem, UT 84058, UPC 7 9238230723 4

by Results RNA, LLC

Reason: Lack of Sterility Assurance and Incorrect/Undeclared excipient: Product was found to contain undeclared colloidal silver
Published: December 26, 2018
Distribution: Nationwide

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Data last updated: September 23, 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.