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Recall totals

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

37,066

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 12, 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

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

FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl 25 mg/25 mL in 0.9% Sodium Chloride Injection, (Concentration = 1mg/mL), 25 mL fill 30 mL Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0303-17, Bar Code 7004030317

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl 10 mg/50 mL in 0.9% Sodium Chloride Injection (Concentration = 0.2 mg/ml) 50 mL fill Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0300-22, Bar Code 70004030022

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride, (Concentration = 0.2mg/ml) 30 mL Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0300-18, Bar Code 70004030018

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride Injection, (Concentration = 0.2 mg/ml) 30 mL fill 35 mL Plungerless Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0300-16, Bar Code 70004030016

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROmorphone HCl 20 mg/100mL in 0.9% Sodium Chloride Injection, 100 mL Grey CADD Cassette (20 mg/100 mL), CII, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0300-63, Bar Code 70004030063

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 2,500 mcg/50 mL in 0.9 % Sodium Chloride Injection (Concentration = 50 mcg/mL) 50 mL Single Dose Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0202-22, Bar code 70004020022,

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL 1,250 mcg/25 mL Injection (Concentration = 50 mcg/mL), 25 mL fill in a 30 mL Single Dose Syringe, RX Only, repackaged by SCA Pharma. SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0200-17, Bar code 70004020017

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 500 mcg/100 mL, Bupivacaine HCl 0.075% in 0.9% Sodium Chloride 100 mL Injection (fentaNYL Concentration = 5 mcg/mL), EPIDURAL USE ONLY, 100 mL Yellow CADD Cassette, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0251-64, Bar Code 70004025164

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 500 mcg/100 mL, Bupivacaine HCl 0.04% in 0.9% Sodium Chloride 100 mL Injection (fentaNYL Concentration = 5 mcg/mL), EPIDURAL USE ONLY, 100 mL Yellow CADD Cassette, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0289-64, Bar Code 70004028964

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 100 mcg/50 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride 50 mL Injection (fentaNYL Concentration = 2 mcg/mL), EPIDURAL USE ONLY, 50 mL fill Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd, Windsor, CT 06095, NDC 70004-0231-22, Bar Code 70004023122

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 200 mcg/100 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride 100 mL Injection, (fentaNYL Concentration = 2 mcg/mL), EPIDURAL USE ONLY, 100 mL Yellow CADD Cassette, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0231-64, Bar Code 70004023164

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 200 mcg/100 mL, Bupivacaine HCl 0.125% in 0.9% Sodium Chloride 100 mL Injection (fentaNYL Concentration = 2 mcg/mL), EPIDURAL USE ONLY, 100 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0231-32, Bar Code 70004023132

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 2,500 mcg/50 mL Injection (Concentration = 50 mcg/mL), INTRAVENOUS USE ONLY, 50 mL Bag, Rx only, SCA Pharma, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0222-30 BAR code 70004022230

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

fentaNYL 2,500 mcg/250 mL in 0.9% Sodium Chloride Injection (Concentration = 10 mcg/mL), 250 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, 877.550.5059, NDC 70004-0229-40 BAR code 70004022940

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Diltiazem HCl 125 mg in 0.9% Sodium Chloride Injection (Concentration = 1mg/mL), 125 mL Bag, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095; NDC 70004-0541-35, Bar Code 70004054135

by SCA Pharmaceuticals, LLC

Reason: Lack of Assurance of Sterility
Published: April 3, 2024
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Roland Foods, LLC.

Product: Roland Tahini; 100% Ground Sesame Seeds; Net WT. 16 OZ. (1 L…
Reason: Product may be contaminated with Salmonella.
Published: April 3, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Nordic Naturals, Inc.

Product: Nordic Naturals Baby s Vitamin D3 liquid, 400 IU (10 mcg) D3…
Reason: Elevated levels of vitamin D3
Published: April 3, 2024
Distribution: Products are distributed to 79 consignee…

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FDA Recall United States Terminated Historical recordClass I

John B. Sanfilippo & Son Inc.

Product: Great Value Honey Roasted Cashews, 8.25oz. plastic can, UPC…
Reason: undeclared milk and coconut
Published: April 3, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Barsotti Juice Company, Inc.

Product: Barsotti Organic Carrot Juice 16 oz. and 64 oz. plastic bott…
Reason: Product was determined to be under processed.
Published: April 3, 2024
Distribution: U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass II

WS Global Inc

Product: Himalayan Pain Relief Tea for Gout and Hangover
Reason: Contains undeclared drugs Diclofenac and Dexamethasone Acetate
Published: April 3, 2024
Distribution: Nationwide

View recall →

Data last updated: September 12, 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.