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Recall totals

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

37,113

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

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 15, 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

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

FDA Recall Terminated Historical recordClass II

AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.

by Teva Pharmaceuticals USA

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC Frazer, PA 19355, Manufactured in Ireland, NDC 59310-111-06

by Teva Pharmaceuticals USA

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-530-08.

by Teva Pharmaceuticals USA

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC , Frazer, PA 19355, Manufactured in Ireland, NDC 59310-520-08

by Teva Pharmaceuticals USA

Reason: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Published: October 27, 2021
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only, Manufactured by: Patheon Pharmaceuticals Inc., Cincinnati, OH 45237; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054. Carton NDC#: 68084-295-21 (Individual Dose NDC: 68084-295-11)

by American Health Packaging

Reason: Failed Dissolution Specifications: results were above specification.
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rocuronium Bromide Injection 50mg/5 mL, 5mL Multi-Dose Vial, Rx only, Manufactured for: Piramal Critical Care, Bethlehem, PA 18017, USA, Manufactured by: Sanovel Ilac, San. Ve Tic. A.S. Istanbul, Turkey, NDC 66794-0228-41

by Piramal Critical Care, Inc.

Reason: Labeling: Label Lacks Warning or Rx Legend: Finished product did not include the statement on the flip cap vial, "WARNING: PARALYZING AGENT"
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7

by Beiersdorf Inc

Reason: cGMP Deviations
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02882 4

by Beiersdorf Inc

Reason: cGMP Deviations
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02880 0

by Beiersdorf Inc

Reason: cGMP Deviations
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Coppertone SPORT Sunscreen Spray 50, (To Deliver) Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 5%, NET WT 1.6 OZ (45 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 41100 00506 9

by Beiersdorf Inc

Reason: Chemical contamination; presence of benzene
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Coppertone SPORT MINERAL 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02870 1

by Beiersdorf Inc

Reason: Chemical contamination; presence of benzene
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7

by Beiersdorf Inc

Reason: Chemical contamination; presence of benzene
Published: October 27, 2021
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02882 4

by Beiersdorf Inc

Reason: Chemical contamination; presence of benzene
Published: October 27, 2021
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02880 0

by Beiersdorf Inc

Reason: Chemical contamination; presence of benzene
Published: October 27, 2021
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Maple Island Inc .

Product: Parent's Choice Rice Baby Cereal. Stage 1, 4+ months. Full…
Reason: Product contains elevated level of inorganic arsenic.
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product: Chocolate & the Chip Pumpkin Spice Cookie Bundt Cake: Rice…
Reason: Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product: Chocolate & the Chip The Sweetie Rice Crispy: Rice crispy…
Reason: Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product: Chocolate & the Chip Brown Butter Rice Crispy Treat - Confe…
Reason: Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published: October 27, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product: Chocolate & the Chip Brown Butter Rice Crispy Treat - Choco…
Reason: Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published: October 27, 2021
Distribution: Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Chocolate and the Chip

Product: Chocolate & the Chip Brown Butter Rice Crispy Treat - Salte…
Reason: Inspection by the California Department of Public Health found undeclared allergens in numerous bakery products.
Published: October 27, 2021
Distribution: Nationwide

View recall →

Data last updated: September 15, 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.