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Recall totals

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

37,139

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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 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 24, 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 III

Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube, Distributed by: Ducere Pharma, LLC New Hope, PA 18938 USA --- UPC 849648000023

by Dr. Reddy's Laboratories, Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the secondary packaging doesnt match the lot number printed on the bottle
Published: November 15, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Betadine Solution Swabstick Povidone-Iodine Solution USP, 10% Dist.by: Purdue Products LP. Stamford, CT 06901-3431 NDC 67618-153-01

by Purdue Pharma, LP

Reason: Subpotent Drug: The laminate used to make the pouches was reversed such that the aluminum layer was in contact with the product causing an exothermic reaction between the free iodine and the aluminum.
Published: November 15, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count bottle (NDC 0591-3771-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA.

by Teva Pharmaceuticals USA

Reason: Failed dissolution specifications; all lots within expiry are being recalled due to out of specification dissolution results.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ROCuronium Bromide 10 mg per mL, 5 mL Fill in single dose syringe, (50 mg / 5 mL Total Dose) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-850-09

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Calcium GLUCOnate 2 g added to 0.9% Sodium Chloride 50 mL Bag, Each bag contains 9.3 mEq Ca++ Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0510-30

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine HCl 100 mcg per mL In 0.9% Sodium Chloride 10 mL Fill Volume in a Single Dose Syringe (1,000 mcg / 10 ml Total Dose), Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR, NDC 70004-0810-12

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

oxyTOCIN 30 units added to Lactated Ringers 500 mL Bag, Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0086-44

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

morphine sulfate 1 mg per mL in 0.9% Sodium Chloride a) Total Volume 100 mL in Single Dose CADD Cassette (Total morphine Dose 100 mg per 100 mL) (NDC 70004-0100-63) b) Total Volume 50 mL in Single Dose Syringe (Total morphine Dose 50 mg / 50 mL) (NDC 70004-0100-22) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL as citrate 2 mcg / mL, ROPIVacaine HCl 0.1%, Total Fentanyl Dose (200 mcg per 100 mL) in 0.9% Sodium Chloride single dose CADD Cassette Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0264-64

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentanyl as citrate 2 mcg per mL BUPIvacaine HCl 0.125% (Total FentaNYL Dose 500 mcg/250 mL) in 0.9% Sodium Chloride 250 mL Bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205. NDC 70004-0231-40

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in 0.9% Sodium Chloride 50 mL (HYDROmorphone Total Dose 1000 mcg) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0331-22

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 mL single-dose syringe (Total Dose Hydromorphone 25 mg/25 mL) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0303-17

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

SUCcinylcholine 20 mg per mL, Total Volume 10 mL in single-dose syringe, (SUCcinylcholine 200 mg / 10 ml) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0910-29

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

A1 Slim, Dietary Supplement Beautifully Slim, capsule, 350 mg, 30-count bottle, A1 Slim LLC Pearland TX 77584, www.A1SLIM.COM, info@a1slim.com Bar-Code A105212014

by Kiriko, LLC.

Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine, making this an unapproved drug for which safety and efficacy have not been established and therefore, subject to recall.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.

by Precision Dose Inc.

Reason: Subpotent Drug: low out of specification results.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The Netherlands; Mfd for: Winthrop U.S., a business of sanofi-aventis U.S. LLC, Bridgewater, NJ 08807; NDC 0955-1746-01.

by Sanofi-Aventis U.S. LLC

Reason: Labeling: Incorrect or Missing Package Insert: authorized generic product was packaged with the incorrect insert for the brand name product Clolar (clofarabine) injection.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.

by AVKARE Inc.

Reason: Failed Impurities/Degradation Specifications: slightly elevated levels of phthalic acid.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Tres Latin Foods

Product: Tres Latin Foods Pupusas, Stuffed Corn Tortillas with Black…
Reason: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10 oz. Pupusas and Black Bean and Sweet Corn 10 oz. Pupusas due to undeclared milk allergen.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Tres Latin Foods

Product: Tres Latin Foods Kale & Pinto Bean pupusas Stuffed Corn Tort…
Reason: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10 oz. Pupusas and Black Bean and Sweet Corn 10 oz. Pupusas due to undeclared milk allergen.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

ASK Foods Inc

Product: taste of Inspirations Classic Red Skin Potato Salad; Net Wt.…
Reason: A.S.K. Foods, Inc. of Palmyra, Pennsylvania is voluntarily recalling one lot of Hannaford Supermarkets Taste Of Inspirations Classic Red Skin Potato Salad Net Wt. 16 oz. (454g) because it may contain undeclared egg.
Published: November 8, 2017
Distribution: ME, NY, MA, NH and VT.

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Data last updated: September 24, 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.