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Recall totals

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

37,115

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 17, 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 II

Baker's Corner Bakery

Product: Oatmeal Butterscotch Cookie, packed in closed bags, 12oz net…
Reason: Shortening is declared but sub-ingredient Soybean Oil is not declared and Butterscotch chip is declared but sub-ingredient Milk is not declared.
Published: September 29, 2021
Distribution: distributed in WA only.

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FDA Recall United States Terminated Historical recordClass II

Baker's Corner Bakery

Product: Chocolate Chip Cookie, packed in closed bags, 12oz net wt.…
Reason: Shortening is declared but sub-ingredient Soybean Oil is not declared and Chocolate chip is declared but sub ingredient Soy Lecithin is not declared.
Published: September 29, 2021
Distribution: distributed in WA only.

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FDA Recall United States Terminated Historical recordClass II

Baker's Corner Bakery

Product: Snickerdoodle Cookie, packed in closed bags, 12oz net wt. T…
Reason: Shortening is declared but sub-ingredient Soybean Oil is not declared.
Published: September 29, 2021
Distribution: distributed in WA only.

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FDA Recall United States Terminated Historical recordClass II

Baker's Corner Bakery

Product: Lemon Thyme Cookies, packed in closed bags, 12oz net wt. Th…
Reason: Shortening is declared but sub-ingredient Soybean Oil is not declared.
Published: September 29, 2021
Distribution: distributed in WA only.

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FDA Recall United States Terminated Historical recordClass II

Baker's Corner Bakery

Product: Oatmeal Cranberry Cookie, packed in closed bags, 12oz net wt…
Reason: Shortening is declared but sub-ingredient Soybean Oil is not declared.
Published: September 29, 2021
Distribution: distributed in WA only.

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FDA Recall United States Terminated Historical recordClass I

Golden Natural Products

Product: Golden Natural Product Inc. brand Dried Apricot Subkhon with…
Reason: Product contains high levels of undeclared sulfites.
Published: September 29, 2021
Distribution: Multiple states

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FDA Recall Terminated Historical recordClass I

AMINOSYN II 15% An Amino Acid Injection, Sulfite-Free, 2000 mL in flexible containers, Rx ONLY, Hospira, Inc., Lake Forest, IL 60045. NDC 0409-7171-17

by ICU Medical Inc

Reason: Presence of Particulate Matter: Particulate matter identified as fibers, hair, and proteinaceous material along with other particles, found in retain smples.
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Spironolactone Ophthalmic Solution 0.005 mg/mL, 15 mL bottles, Rx only, Greenpark Compounding Pharmacy

by Prescription Labs Inc dba Greenpark

Reason: Lack of Assurance of Sterility
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Betamethasone Dipropionate Lotion USP (Augmented), 0.05%, packaged in a) 30 mL bottle (NDC 61748-480-30), b) 60 mL bottle (NDC 61748-480-60), Rx only, Manufactured by: Hi-Tech Pharmacal Co. Inc., Amityville,NY 11701

by Akorn, Inc.

Reason: Failed impurities/degradation specification: Out of Specification for an unknown impurity observed in topical product.
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Glycopyrrolate Injection, USP 4mg per 20mL, 20 mL Multi-Dose Vials, Rx only, Mfd for Meitheal Pharmaceuticals, Chicago, IL 60631. NDC 71288-408-21

by Meitheal Pharmaceuticals Inc

Reason: Failed Impurities/Degradation Specifications
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Lidocaine Hydrochloride Topical Solution, USP, 4% , 50 mL glass bottles, Rx Only, Teligent Pharma Inc. Buena, New Jersey 08310, NDC 52565-009-50.

by Teligent Pharma, Inc.

Reason: Superpotent Drug
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Kroger 70% Isopropyl Alcohol First Aid Antiseptic 32 FL OZ (1 QT) 946 mL 5 Dist. By The Kroger Co., Cincinnati, Ohio 45202 NDC 30142-810-45, UPC 0 11110 37049

by Vi-Jon, Inc.

Reason: Labeling: Label Mix-Up.The recall has been initiated after receiving one complaint about incorrect labeling.The primary label on the front and back label on some of the bottles have 70% Isopropyl Alcohol affixed to the containers. However, the product inside the bottle is Hydrogen Peroxide, Topical Solution USP with active ingredient Hydrogen Peroxide (stabilized) 3%, 32 FL Ounces
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 NDC 0378-3231-93

by Viatris

Reason: Failed Impurities/Degradation Specifications; out of specification for Related Compound
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Hydro Pinapple Burn Max Health Thach Dua, packaged in a box containing 20g x 10 goi/sachets, MATXI CORP, UPC 8 936188 880108

by Ebay Seller - John Nguyen

Reason: Marketed without an approved NDA/ ANDA - presence of undeclared sibutramine
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%), packaged in a) 8.45 fl oz (250 mL) bottles and b) 33.81 fl oz (1L) bottles, Distributed by: Asimex International LLC, 9100 S Dadeland Blvd, Ste 912, Miami, FL 33156, COUNTRY OF ORIGIN: MEXICO.

by Grupo Asimex de Mexico SA de CV

Reason: CGMP Deviations: All other lots are being recalled because they were manufactured under the same conditions as the product lots found to contain methanol.
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%), packaged in a) 8.45 fl oz (250 mL) bottles and b) 33.81 fl oz (1L) bottles, Distributed by: Asimex International LLC, 9100 S Dadeland Blvd, Ste 912, Miami, FL 33156, COUNTRY OF ORIGIN: MEXICO.

by Grupo Asimex de Mexico SA de CV

Reason: Chemical Contamination: FDA analysis found the product contains methanol, additionally it is sub-potent for ethanol content.
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Oxycodone Hydrochloride Tablets, USP, 10 mg, 100 count bottle, Rx only, Marketed by: Rhodes Pharmaceuticals L.P., Coventry RI 02816, Manufactured by: Purdue Pharma L.P., Stanford, CT 06901 NDC 42858-002-01

by Rhodes Pharmaceuticals, L.P.

Reason: Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found in one bottle
Published: September 22, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Loki Fish Company - Office

Product: Loki Fish Wild Keta Salmon Lox, packaged in a 4 oz. plastic…
Reason: Potential to be contaminated with Listeria monocytogenes.
Published: September 22, 2021
Distribution: distributed in Oregon and Washington.

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FDA Recall United States Terminated Historical recordClass II

Naturo Aid Pharmaceutical Inc.

Product: Vita Aid SynerClear (Chocolate), VA-012. The product is a p…
Reason: Undeclared Milk. Products may be contaminated with milk residue.
Published: September 22, 2021
Distribution: Distributed in Arizona, California, Flor…

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FDA Recall United States Terminated Historical recordClass II

Naturo Aid Pharmaceutical Inc.

Product: Vita Aid SynerClear (Vanilla), VA-924. The product is a pow…
Reason: Undeclared Milk. Products may be contaminated with milk residue.
Published: September 22, 2021
Distribution: Distributed in Arizona, California, Flor…

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Data last updated: September 17, 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.