FoodJul 1, 2026
Spring & Mulberry Net Wt recall — FDA H-1098-2026
Potential Salmonella contamination
Class IFDA: OngoingSpring & Mulberry Inc.
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
September 2026300 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categories
2026 recalls — page 41
Records are ordered by the best available source date.
FoodJul 1, 2026
Alb-USA Enterprises El David Gelee, Bonbons with fruits Soft & Juicy, 400g recall — FDA H-1110-2026
Undeclared colors (FD&C Yellow 5 and FD&C Red 40).
Class IIFDA: OngoingAlb-USA Enterprises Inc
FoodJul 1, 2026
Spring & Mulberry Net Wt recall — FDA H-1097-2026
Potential Salmonella contamination
Class IFDA: OngoingSpring & Mulberry Inc.
FoodJul 1, 2026
Spring & Mulberry Net Wt recall — FDA H-1099-2026
Potential Salmonella contamination
Class IFDA: OngoingSpring & Mulberry Inc.
FoodJul 1, 2026
Spring & Mulberry Net Wt recall — FDA H-1104-2026
Potential Salmonella contamination
Class IFDA: OngoingSpring & Mulberry Inc.
FoodJul 1, 2026
Produce Innovations Roast beef and cheddar closed face sandwich packed in clear recall — FDA H-1111-2026
Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich
Class IIIFDA: TerminatedProduce Innovations
FoodJul 1, 2026
George J Howe Company 25# Sunflower Seeds C/S recall — FDA H-1123-2026
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Class IFDA: OngoingGeorge J Howe Company, Inc.
FoodJul 1, 2026
Spring & Mulberry Net Wt recall — FDA H-1101-2026
Potential Salmonella contamination.
Class IFDA: OngoingSpring & Mulberry Inc.
FoodJul 1, 2026
George J Howe Company 6/11oz No Salt Sunflower Seeds recall — FDA H-1119-2026
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Class IFDA: OngoingGeorge J Howe Company, Inc.
FoodJul 1, 2026
Spring & Mulberry Net Wt recall — FDA H-1100-2026
Potential Salmonella contamination
Class IFDA: OngoingSpring & Mulberry Inc.
FoodJul 1, 2026
Champion Foods Motor City Pizza Co recall — FDA H-1095-2026
potential salmonella contamination
Class IIFDA: TerminatedChampion Foods, LLC
FoodJul 1, 2026
boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET recall — FDA H-1133-2026
Undeclared allergen, sesame.
Class IIFDA: OngoingBoichik Bagels, Inc.
VehicleJun 30, 2026
Ford motor recall — NHTSA campaign 26V418000
Ford Motor Company (Ford) is recalling certain 2024-2026 Mustang and 2025-2026 Mustang GTD vehicles. During certain cold temperature conditions, the windshield wipers may function only at…
motorFord Motor Company
VehicleJun 30, 2026
Chrysler gear position indication (prndl) recall — NHTSA campaign 26V413000
Chrysler (FCA US, LLC) is recalling certain 2022-2024 Jeep Grand Cherokee, 2023 Jeep Wagoneer, 2024 Jeep Grand Cherokee L, and Jeep Wagoneer L vehicles. A software error may cause the…
gear position indication (prndl)Chrysler (FCA US, LLC)
VehicleJun 30, 2026
Rogue gear position indication (prndl) recall — NHTSA campaign 26V419000
Nissan North America, Inc. (Nissan) is recalling certain 2026 Rogue vehicles. The instrument panel may not display the transmission gear selection indicator. As such, these vehicles fail to…
gear position indication (prndl)Nissan North America, Inc.
VehicleJun 26, 2026
Nissan Sentra driveshaft recall — NHTSA campaign 26V410000
Nissan North America, Inc. (Nissan) is recalling certain 2025 Nissan Sentra vehicles. The front left-side driveshaft may not be fully seated in the continuously variable transmission (CVT)…
driveshaftNissan North America, Inc.
VehicleJun 24, 2026
Bronco body recall — NHTSA campaign 26V403000
Ford Motor Company (Ford) is recalling certain 2022-2026 Bronco vehicles. The fender flares may not be properly secured and detach from the vehicle.
bodyFord Motor Company
VehicleJun 24, 2026
Ford automatic transmission recall — NHTSA campaign 26V402000
Ford Motor Company (Ford) is recalling certain 2018-2021 Navigator, Expedition, 2020-2021 Explorer, Lincoln Aviator, and 2021 F-150 vehicles. The transmission park pawl may engage while the…
automatic transmissionFord Motor Company
VehicleJun 24, 2026
Hyundai Motor instrument cluster/panel recall — NHTSA campaign 26V400000
Hyundai Motor America (Hyundai) is recalling certain 2025-2026 Tucson, Tucson Hybrid, Tucson Plug-In Hybrid Electric (PHEV) vehicles. Due to a software error, the instrument panel display…
instrument cluster/panelHyundai Motor America
Medical DeviceJun 24, 2026
Medline convenience kits: PORT A CATH DYNJ906818A recall — FDA Z-2443-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y PACEMAKER DYNJ56297C recall — FDA Z-2418-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
Beta Bionics iLet Bionic Pancreas, REF: BB1001 recall — FDA Z-2513-2026
The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfully…
Class IIFDA: OngoingBeta Bionics, Inc.
Medical DeviceJun 24, 2026
Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT recall — FDA Z-2439-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT, ASC T&A, CONWAY recall — FDA Z-2491-2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish,…
Class IIFDA: OngoingMedline Industries, LP
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.