FoodMar 4, 2026
Oregon Potato Company IQF Blueberry recall — FDA H-0522-2026
Listeria monocytogenes
Class IFDA: CompletedOregon Potato Company LLC
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026373 records · 4 categoriesMay 2026330 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026329 records · 4 categoriesJanuary 2026210 records · 4 categories
2026 recalls — page 75
Records are ordered by the best available source date.
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
About the 2026 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.