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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 recalls
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 13,601–13,620 of 21,084 recalls

FDA Recall United States Terminated Historical recordClass II

NatureBox, Inc.

Product
NatureBox Sticks 'n Stones; roasted nuts with sesame sticks.…
Reason
Firm received notification that a consumer found a peanut in NatureBox Sticks 'n Stones snack mix that contains Cashews and Almonds, not peanuts.
Published
August 9, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Professional Complementary Health Formulas, LLC

Product
Professional Formulas Sublinqual B12 High-Potency dietary su…
Reason
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
Published
August 9, 2017
Distribution
distributed in AZ, CA, CO, CT, FL, GA, H…

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product
Clif Kid Zbar Protein Chocolate Mint 10-pack, 150-count, 5-…
Reason
Undeclared peanuts and/or tree nuts.
Published
August 9, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product
Clif Kid Zbar Protein Chocolate Chip 10-pack, 150-count, 5-…
Reason
Undeclared peanuts and/or tree nuts.
Published
August 9, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product
Clif Builders Chocolate Mint 12-count, 6-pack, 7-pack, Snac…
Reason
Undeclared peanuts and/or tree nuts.
Published
August 9, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product
Clif Kid Zbar Protein Variety Pack 30-count
Reason
Undeclared peanuts and/or tree nuts.
Published
August 9, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Clif Bar & Company

Product
Clif Builders Variety Pack Chocolate Peanut Butter and Choco…
Reason
Undeclared peanuts and/or tree nuts.
Published
August 9, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-0833-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Chloride 20 meq Added to Sodium Chloride 0.9% 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0832-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine 100 mg in 0.9% Sodium Chloride 250 mL Bag, Rx only, SCA Pharmaceuticals 882PHENYLephrine 100 mg 1 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0813-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine 10 mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-0811-59

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride 250 mL Bag, Preservative Free, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0811-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine HCl 25 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0810-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

NORepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0775-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

NORepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0774-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

NORepinephrine 4 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0771-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

EPINEPHrine HCl 4 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0613-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate 5 mg/mL in NS 5 mL Fill in 12 mL Syringe (25 mg), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0600-11

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL 3 mcg/mL + BUPIvacaine 0.1% in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0290-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

fentaNYL 10 mcg/mL PF in Sodium Chloride 250 mL (Total Dose=2500 mcg), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0229-40

by SCA Pharmaceuticals

Reason
Lack of Assurance of Sterility; product has the potential to leak.
Published
August 2, 2017
Distribution
Nationwide

View recall →

Data last updated:

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.