Latest U.S. Recalls — FDA & NHTSA Records

Latest records

Latest recalls — page 75

The newest recall records with useful source details are listed here.

FoodMar 4, 2026

Oregon Potato Company IQF Blueberry recall — FDA H-0522-2026

Listeria monocytogenes

Class IFDA: CompletedOregon Potato Company LLC

FoodMar 4, 2026

SB FOOD Yoyo Gummy Assorted Flavor, 2.8 Oz recall — FDA H-0527-2026

The products contain an unallowed color Carmoisine (E122) - Acid Red 14.

Class IIFDA: OngoingSB FOOD LLC

FoodMar 4, 2026

Gerber Products Company dba Nestle Infant Net Wt recall — FDA H-0518-2026

Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.

Class IIFDA: OngoingGerber Products Company dba Nestle Infant Nutrition

FoodMar 4, 2026

SB FOOD Yoyo Gummy Tropical Flavor, 2.8 Oz recall — FDA H-0528-2026

The products contain an unallowed color Carmoisine (E122) - Acid Red 14.

Class IIFDA: OngoingSB FOOD LLC

FoodMar 4, 2026

J2C Hawaii Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel recall — FDA H-0523-2026

Ingredients List declares peanut but the Contains statement does not declare peanut

Class IIFDA: TerminatedJ2C Hawaii LLC

FoodMar 4, 2026

Valley Springs Steamed Distilled Water recall — FDA H-0536-2026

Water was bottled under insanitary conditions.

Class IIFDA: OngoingValley Springs Artesian Gold, LLC

FoodMar 4, 2026

SB FOOD Yoyo Gummy Grape Plus Flavor, 2.8 Oz recall — FDA H-0529-2026

The products contain an unallowed color Carmoisine (E122) - Acid Red 14.

Class IIFDA: OngoingSB FOOD LLC

FoodMar 4, 2026

Navitas, LLC NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ recall — FDA H-0533-2026

Potential contamination with Salmonella.

Class IFDA: OngoingNavitas, LLC.

FoodMar 4, 2026

TENGEN USA TRADING YO!MAN LETTUCE recall — FDA H-0526-2026

Product contains undeclared cyclamates.

Class IIIFDA: TerminatedTENGEN USA TRADING CORP

FoodMar 4, 2026

TENGEN USA TRADING YO!MAN CUCUMBER recall — FDA H-0525-2026

Product contains undeclared cyclamates.

Class IIIFDA: TerminatedTENGEN USA TRADING CORP

FoodMar 4, 2026

Valley Springs 100% Natural Bottled Water recall — FDA H-0535-2026

Water was bottled under insanitary conditions.

Class IIFDA: OngoingValley Springs Artesian Gold, LLC

DrugMar 4, 2026

C20H10NA2O5 FLUORESCEIN SODIUM OPHTHALMIC STRIPS CHNaO Fluorescein Sodium Ophthalmic Strips recall — FDA D-0350-2026

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Class IIFDA: OngoingWizcure Pharmaa Private Limited

DrugMar 4, 2026

Agebox iKids-Growth (Day Formula) capsules, 60-count bottles, Manufactured Exclusively For recall — FDA D-0344-2026

Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

Class IIFDA: OngoingAgebox

DrugMar 4, 2026

Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops Advanced Dry Eye Relief Revitalizing recall — FDA D-0348-2026

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Class IIFDA: OngoingWizcure Pharmaa Private Limited

DrugMar 4, 2026

Agebox iKids-Growth (Night Formula), 60-count bottles, Manufactured Exclusively For: AGEBOX recall — FDA D-0345-2026

Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

Class IIFDA: OngoingAgebox

DrugMar 4, 2026

Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP recall — FDA D-0349-2026

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Class IIFDA: OngoingWizcure Pharmaa Private Limited

DrugMar 4, 2026

ADBRY recall — FDA D-0339-2026

Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.

Class IIFDA: OngoingLEO PHARMA INC

DrugMar 4, 2026

Vista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, 10 ml. recall — FDA D-0347-2026

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Class IIFDA: OngoingWizcure Pharmaa Private Limited

DrugMar 4, 2026

Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose recall — FDA D-0341-2026

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

Class IIFDA: OngoingAvKARE

DrugMar 4, 2026

Eptifibatide Injection, 75 mg/100 mL vial for weight-adjusted bolus dosing, 1x100 mL recall — FDA D-0343-2026

Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial…

Class IIIFDA: OngoingSlate Run Pharmaceuticals

DrugMar 4, 2026

Wizcure Pharmaa Private Vista Tears Polyethylene Glycol 400 0.4% w/v, Propylene Glycol 0.3% recall — FDA D-0346-2026

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Class IIFDA: OngoingWizcure Pharmaa Private Limited

DrugMar 4, 2026

Wizcure Pharmaa Private Bio Glo Fluorescein Sodium Ophthalmic Strips USP, 300 diagnostic recall — FDA D-0351-2026

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Class IIFDA: OngoingWizcure Pharmaa Private Limited

DrugMar 4, 2026

Wizcure Pharmaa Private BioGlo Fluorescein Sodium Ophthalmic Strips USP, 100 diagnostic recall — FDA D-0352-2026

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Class IIFDA: OngoingWizcure Pharmaa Private Limited

VehicleMar 3, 2026

Ford motor recall — NHTSA campaign 26V117000

Ford Motor Company (Ford) is recalling certain 2020-2022 Explorer, Escape, Lincoln Aviator, and Lincoln Corsair vehicles. The windshield wiper motor may fail and prevent the windshield…

motorFord Motor Company

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