FoodDec 24, 2025
Lexunder Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged recall — FDA H-0309-2026
Contaminated with Salmonella
Class IFDA: TerminatedLexunder Inc
Latest records
Latest recalls — page 123
The newest recall records with useful source details are listed here.
FoodDec 24, 2025
Dough-To-Go Linzer Hearts Baked Cut Out Cookies UPC 0 44964 22072 2 72 recall — FDA H-0364-2026
Undeclared Milk and FD&C Blue #1.
Class IIFDA: OngoingDough-To-Go Inc
FoodDec 24, 2025
MAMTAKIM Belevini BICHKI, Dried Salted Whole Smelts, Net recall — FDA H-0312-2026
Clostridium botulinum (uneviscerated fish)
Class IFDA: TerminatedMAMTAKIM, Inc.
FoodDec 24, 2025
The New York Milk Bank Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic recall — FDA H-0308-2026
Foreign object
Class IIFDA: TerminatedThe New York Milk Bank, Inc.
VehicleDec 23, 2025
Volvo Car USA back over prevention software recall — NHTSA campaign 25V908000
Volvo Car USA, LLC (Volvo Car) is recalling certain 2021-2025 XC40, 2022 V90, 2022-2024 C40BEV, 2022-2025 S90, V90CC, XC60, 2023-2025 S60, V60, V60CC, XC90, and 2025 EC40, and EX40…
back over prevention softwareVolvo Car USA, LLC
VehicleDec 23, 2025
Rogue spare tire recall — NHTSA campaign 25V912000
Nissan North America, Inc. (Nissan) is recalling certain 2026 Rogue vehicles. The incorrect-size spare tire may have been installed, which does not match the tire size and inflation…
spare tireNissan North America, Inc.
VehicleDec 19, 2025
Volkswagen Group of retractor recall — NHTSA campaign 25V899000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2025 SQ6 E-Tron, SQ6 Sportback E-Tron, Q6 Sportback E-Tron, A6, A5, A6 Sportback E-Tron, Q6 E-Tron, S5, and S6 Sportback E-Tron…
retractorVolkswagen Group of America, Inc.
VehicleDec 19, 2025
2019-2026 camera recall — NHTSA campaign 25V900000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2019-2026 vehicles. Please see the recall report for a complete list of models. A software error may prevent the rearview…
cameraVolkswagen Group of America, Inc.
VehicleDec 19, 2025
Tucson trailer hitch recall — NHTSA campaign 25V893000
Hyundai Motor America (Hyundai) is recalling certain 2022-2024 Tucson vehicles equipped with an optional Mobis tow hitch wiring harness. The wiring harness may have been installed…
trailer hitchHyundai Motor America
VehicleDec 18, 2025
Maverick dashboard recall — NHTSA campaign 25V884000
Ford Motor Company (Ford) is recalling certain 2025-2026 Maverick vehicles. The instrument panel cover may separate when the air bag deploy.
dashboardFord Motor Company
VehicleDec 18, 2025
Bronco camera recall — NHTSA campaign 25V888000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco vehicles equipped with 8-inch SYNC infotainment screens that were previously repaired incorrectly under recall number 23V165.…
cameraFord Motor Company
VehicleDec 18, 2025
Forester hinge and attachments recall — NHTSA campaign 25V889000
Subaru of America, Inc. (Subaru) is recalling certain 2026 Forester vehicles. These vehicles may have been manufactured with an incorrect and/or incorrectly oriented rear hatch support…
hinge and attachmentsSubaru of America, Inc.
VehicleDec 18, 2025
Chrysler air bag control module recall — NHTSA campaign 25V882000
Chrysler (FCA US, LLC) is recalling certain 2025 Ram 2500 Pickup, 3500 Pickup, 3500 Cab Chassis, 4500 Cab Chassis, and 5500 Cab Chassis trucks. A software error in the occupant restraint…
air bag control moduleChrysler (FCA US, LLC)
VehicleDec 17, 2025
Toyota Motor Engineering & Manufacturing seat belt anchor recall — NHTSA campaign 25V872000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2024-2025 Highlander and Highlander Hybrid vehicles. The third row center seat belt roof anchor may have been…
seat belt anchorToyota Motor Engineering & Manufacturing
Medical DeviceDec 17, 2025
C.R. Bard BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF recall — FDA Z-0908-2026
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
Class IIFDA: OngoingC.R. Bard Inc.
Medical DeviceDec 17, 2025
FORZA" PTC Spacer System recall — FDA Z-0892-2026
Labeling contains claims that are not consistently present.
Class IIIFDA: OngoingOrthofix U.S. LLC
Medical DeviceDec 17, 2025
Pillar" SA PTC Spacer System recall — FDA Z-0893-2026
Labeling contains claims that are not consistently present.
Class IIIFDA: OngoingOrthofix U.S. LLC
Medical DeviceDec 17, 2025
Draeger ErgoStar CM 55 recall — FDA Z-0592-2026
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Class IFDA: OngoingDraeger, Inc.
Medical DeviceDec 17, 2025
FIREBIRD" SI Fusion System recall — FDA Z-0894-2026
Labeling contains claims that are not consistently present.
Class IIIFDA: OngoingOrthofix U.S. LLC
Medical DeviceDec 17, 2025
Medline Industries Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item recall — FDA Z-0901-2026
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceDec 17, 2025
MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C recall — FDA Z-0886-2026
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceDec 17, 2025
Waldemar Link GmbH & Co. KG Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling recall — FDA Z-0890-2026
The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceDec 17, 2025
Medline Industries DEXLOCK Achilles Repair Implant Kits, MAKT4520 recall — FDA Z-0911-2026
There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill guide may prolong the surgical…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceDec 17, 2025
Stryker MV3 bariatric bed, Part Number 5900000001 recall — FDA Z-0918-2026
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for…
Class IIFDA: OngoingStryker Medical Division of Stryker Corporation
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