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Recall totals

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

37,497

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,881

Class I recallsReasonable probability of serious health consequences

24,543

Class II recallsTemporary or medically reversible health consequences

2,935

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 2,098 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-all-cheddar-cheese-products-because-possible-health-riskPublished November 10, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 10, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,543
Class I	9,881
Class III	2,935
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: January 31, 2017Historical recordClass II

Real Fudge

Product: Salted Caramel Fudge, brand Real Fudge. Product is sold in…
Reason: Salted Caramel Fudge is recalled due to undeclared blue #1.
Published: December 28, 2016
Distribution: Distributed in Idaho, Maryland, Nevada,…

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FDA Recall United States TerminatedTerminated: January 31, 2017Historical recordClass II

Real Fudge

Product: Dark Chocolate Fudge, brand Real Fudge. Product is sold i…
Reason: Dark Chocolate Fudge is recalled due to undeclared blue #1.
Published: December 28, 2016
Distribution: Distributed in Idaho, Maryland, Nevada,…

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FDA Recall United States TerminatedTerminated: January 31, 2017Historical recordClass II

Real Fudge

Product: Rocky Road Fudge, brand Real Fudge. Product is sold in cle…
Reason: Rocky Road Fudge is recalled due to undeclared blue #1.
Published: December 28, 2016
Distribution: Distributed in Idaho, Maryland, Nevada,…

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FDA Recall United States TerminatedTerminated: January 31, 2017Historical recordClass II

Real Fudge

Product: Peanut Butter Fudge, brand Real Fudge. Product is sold in cl…
Reason: Peanut Butter Fudge is recalled due to undeclared blue #1.
Published: December 28, 2016
Distribution: Distributed in Idaho, Maryland, Nevada,…

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FDA Recall United States TerminatedTerminated: January 31, 2017Historical recordClass II

Real Fudge

Product: Nutty fudge, brand Real Fudge. Product is sold in clear plas…
Reason: Nutty fudge is recalled due to undeclared blue #1.
Published: December 28, 2016
Distribution: Distributed in Idaho, Maryland, Nevada,…

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FDA Recall United States TerminatedTerminated: January 31, 2017Historical recordClass II

Real Fudge

Product: Plain Fudge, brand Real Fudge. Product is sold in clear pla…
Reason: Plain Fudge is recalled due to undeclared blue #1.
Published: December 28, 2016
Distribution: Distributed in Idaho, Maryland, Nevada,…

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FDA Recall United States TerminatedTerminated: January 31, 2017Historical recordClass II

Real Fudge

Product: White Fudge Oreo, brand Real Fudge. Product is sold in clear…
Reason: White Fudge Oreo is recalled due to undeclared wheat and blue # 1.
Published: December 28, 2016
Distribution: Distributed in Idaho, Maryland, Nevada,…

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FDA Recall United States TerminatedTerminated: June 20, 2018Historical recordClass II

Midwest International Corp

Product: Malayuguo, USA jiazhoufengwei, Fish, NET WT 4.2oz (120g)
Reason: The product is a low acid canned food (LACF) without a registered manufacturer and scheduled process.
Published: December 28, 2016
Distribution: CA, IL, NY, MD, MA, KY, TX and VA

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FDA Recall United States TerminatedTerminated: June 20, 2018Historical recordClass II

Midwest International Corp

Product: Qiejidingxiangyu, USA jiazhoufengwei, Fish, NET WT 4.2oz (12…
Reason: The product is a low acid canned food (LACF) without a registered manufacturer and scheduled process.
Published: December 28, 2016
Distribution: CA, IL, NY, MD, MA, KY, TX and VA

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FDA Recall United States TerminatedTerminated: June 20, 2018Historical recordClass II

Midwest International Corp

Product: Heihujiaoyupai, USA jiazhoufengwei, Fish, NET WT 4.2oz (120g…
Reason: The product is a low acid canned food (LACF) without a registered manufacturer and scheduled process.
Published: December 28, 2016
Distribution: CA, IL, NY, MD, MA, KY, TX and VA

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FDA Recall United States TerminatedTerminated: June 29, 2017Historical recordClass I

Whole Foods Market Brand 365, Llc

Product: CROISSANT CHOCOLATE 6 PK
Reason: Product contains undeclared eggs.
Published: December 28, 2016
Distribution: Select Whole Foods Market stores in Penn…

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FDA Recall United States TerminatedTerminated: June 29, 2017Historical recordClass II

Whole Foods Market Brand 365, Llc

Product: MULTI GRAIN CROISSANT 6 PK
Reason: Product contains undeclared eggs.
Published: December 28, 2016
Distribution: Select Whole Foods Market stores in Penn…

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FDA Recall United States TerminatedTerminated: June 29, 2017Historical recordClass II

Whole Foods Market Brand 365, Llc

Product: CROISSANT 6 PK
Reason: Product contains undeclared eggs.
Published: December 28, 2016
Distribution: Select Whole Foods Market stores in Penn…

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FDA Recall TerminatedTerminated: July 12, 2017Historical recordClass III

Methylprednisolone Tablets, USP, 16 mg, 50-count bottles, Rx only, Manufactured by Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-003-14.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration date of 02/0218 is printed on the container label instead of the correct expiration date of 02/2018.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2020Historical recordClass II

Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-067-12

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2020Historical recordClass II

Ropivacaine HCl 0.25% in 0.9% Sodium Chloride, 100 mL Bag, Epidural Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-185-75

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2020Historical recordClass II

Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) Single-Dose Syringe, Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-064-15

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2020Historical recordClass II

Oxytocin 30 USP Units Added to 0.9% Sodium Chloride, 500 mL Bag, Single-Dose Bag, Injection Solution for IV Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-056-30

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2020Historical recordClass II

Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) Single-Dose Syringe, For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-046-15

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 29, 2020Historical recordClass II

Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride, 100 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-160-75

by Cantrell Drug Company

Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Published: December 21, 2016
Distribution: Nationwide

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Data last updated: November 10, 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.