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Recall totals

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

37,118

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

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Source: FDA and USDA public dataLast updated September 20, 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

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass I

Rachael's Food Corporation

Product: Rachael's SPRINGFIELD SMOKED FISH Smoked Trout 6 oz, UPC: 04…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: January 10, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Rachael's Food Corporation

Product: SPRINGFIELD SMOKED FISH Smoked Sable, Catch weight, UPC: N/A
Reason: Product may be contaminated with Listeria monocytogenes.
Published: January 10, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Auryxia (ferric citrate) tablets, 210 mg , 200-count bottles, RX ONLY, Manufactured for and distributed by: Keryx Biopharmaceticals, Inc. One Marina Park Drive, 12th Floor, Boston, MA 02210 USA. NDC 59922-631-01

by Keryx Biopharmaceuticals, Inc.

Reason: Presence of Foreign Substance: Reports have been received of damaged StripPax packets containing silica gel desiccant potentially allowing the silica gel granules to make contact with Auryxia tablets in the bottle.
Published: January 3, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-165-78

by PharMEDium Services, LLC

Reason: Labeling: Incorrect or Missing Lot and/or Exp. Date
Published: January 3, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg per mL , For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-455-78

by PharMEDium Services, LLC

Reason: Labeling: Incorrect or Missing Lot and/or Exp. Date
Published: January 3, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Volume 1 mg per mL (2 mg per 2 mL), For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-259-28

by PharMEDium Services, LLC

Reason: Labeling: Incorrect or Missing Lot and/or Exp. Date
Published: January 3, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

All Sterile Products within expiry

by Vital Rx, Inc. dba Atlantic Pharmacy and Compounding

Reason: Lack of Assurance of Sterility .
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, Nasal Decongestant. 24 softgel tablets per paper carton, Distributed by Perrigo, Allegan, MI 49010, NDC 70085-151-01

by L. Perrigo Company

Reason: Microbial Contamination of Non-Sterile Products
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% Dextrose, Rx Only, (2 mg/mL), 100 mL Flexible Bag, Manufactured for: Claris LifeScience Inc. North Brunswick NJ 08902 by Claris Injectables Ltd. Gujarat, India UPC 336000008242 NDC 36000-008-249

by Claris Lifesciences Inc

Reason: Superpotent
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

NATURAL HERBAL COFFEE AMPT, sold in 25g packages (UPC 6942630905), 10-count packages per box (UPC 6942630912); Manufactured For: The Ampt Life, LLC.

by The Ampt Life, LLC

Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to contain undeclared sildenafil and tadalafil and undeclared milk. The presence of sildenafil and tadalafil makes AMPT Natural Herbal Coffee an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall. Additionally, this product has been found to contain undeclared milk, milk is recognized as one of the foods reported to have caused deaths due to anaphylactic shock in persons with underlying hypersensitivities.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP, 90mcg/20mcg), 28 tablet dispenser (blister foil unit), Rx only, Manufactured by: Warner Chilcott Company, LLC Fajardo, Puerto Rico 00738: Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054 USA, NDC-52544-295-28

by Teva Pharmaceuticals USA

Reason: Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed on the blister foil and package insert, however,all tablets are active.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Fluconazole Injection, USP, 2 mg/mL, a) 50 mL (NDC 336000-261-10) and b) 100 mL (NDC 33600-002-10), Rx Only, Manufactured for: Claris LifeSciences, Inc. North Brunswick, NJ 08902 By: Claris Injectables Ltd., Gujarat, India

by Renaissance Lakewood, LLC

Reason: Superpotent
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02

by Pfizer Inc.

Reason: Presence of Particulate Matter: glass particulate found in vial
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by LaBri's Body Health.

by EZWeightLossTX LLC

Reason: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to be tainted with sibutramine making these unapproved drugs.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.

by EZWeightLossTX LLC

Reason: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to be tainted with sibutramine making these unapproved drugs.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Lorazepam Oral Concentrate, USP, 2 mg/mL, 30 mL bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Branchburg, NJ 08876. Distributed by: Amneal Pharmaceuticals, Glasgow, KY 42141. NDC 65162-687-84

by Amneal Pharmaceuticals of New York, LLC

Reason: Defective Delivery System: the dropper measurement markings may be reversed, shifted or missing.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (200 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-61.

by Advanced Pharma Inc.

Reason: Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj, USP QS 5 mL (200 mcg per mL), 5 mL Sterile single dose syringe, packaged in 8 x 5 (FORTY) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-863-67.

by Advanced Pharma Inc.

Reason: Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NitroGlycerin 100 mcg/mL QS 5% Dextrose Inj, USP (2 mg per 20 mL) 20 mL Sterile single dose syringe, packaged in 10 x 5 (FIFTY) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-818-62.

by Advanced Pharma Inc.

Reason: Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Published: December 27, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (100 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054, NDC 15082-818-61.

by Advanced Pharma Inc.

Reason: Stability Data Does Not Support Expiry: lots do not have stability that supports the use of the container system.
Published: December 27, 2017
Distribution: Nationwide

View recall →

Data last updated: September 20, 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.