FoodNov 19, 2025
Professional Botanicals Tense-X recall — FDA H-0183-2026
Products contains Magnesium Salicylate.
Class IIFDA: TerminatedProfessional Botanicals, Inc.
Latest records
Latest recalls — page 142
The newest recall records with useful source details are listed here.
FoodNov 19, 2025
Singh Trading Inc. DBA Roshni Foods Roshni Cinnamon Powder, 3.5 oz recall — FDA H-0172-2026
Product may contain elevated levels of lead and chromium.
Class IIFDA: TerminatedSingh Trading Inc. DBA Roshni Foods
FoodNov 19, 2025
Lotus Vaping Technologies Monarch Premium Kratom White Elephant powder is packaged in recall — FDA H-0188-2026
Product has the potential to be contaminated with Salmonella
Class IFDA: TerminatedLotus Vaping Technologies, LLC
FoodNov 19, 2025
Lotus Vaping Technologies Monarch Premium Kratom Green Maeng Da powder is packaged in recall — FDA H-0186-2026
Product has the potential to be contaminated with Salmonella
Class IFDA: TerminatedLotus Vaping Technologies, LLC
FoodNov 19, 2025
Pacific International Marketing CA 93912 PRODUCE OF U.S.A recall — FDA H-0176-2026
Potential contamination with Salmonella.
Class IFDA: TerminatedPacific International Marketing
FoodNov 19, 2025
Pacific International Marketing Carton Label: PACIFIC STRAIGHT FROM THE FIELDS FRESH HERBS recall — FDA H-0177-2026
Potential contamination with Salmonella.
Class IFDA: TerminatedPacific International Marketing
FoodNov 19, 2025
Professional Botanicals Total Comfort recall — FDA H-0182-2026
Products contains Magnesium Salicylate.
Class IIFDA: TerminatedProfessional Botanicals, Inc.
FoodNov 19, 2025
GBC Food Services Peach Salsa recall — FDA H-0199-2026
Peaches provided by Moonlight Peaches potentially contaminated with Listeria.
Class IFDA: TerminatedGBC Food Services, LLC
FoodNov 19, 2025
Professional Botanicals Nutra Calm recall — FDA H-0181-2026
Products contains Magnesium Salicylate.
Class IIFDA: TerminatedProfessional Botanicals, Inc.
FoodNov 19, 2025
JFE FRANCHISING Peach Salsa - $5.99-16 oz 639123940636 packaged in clear recall — FDA H-0200-2026
Peaches provided by Moonlight Peaches potentially contaminated with Listeria.
Class IFDA: TerminatedJFE FRANCHISING INC
FoodNov 19, 2025
Pacific International Marketing CA 93912 Carton Sticker Label: Conv Italian Parsley 60 Ct recall — FDA H-0174-2026
Potential contamination with Salmonella.
Class IFDA: TerminatedPacific International Marketing
FoodNov 19, 2025
Seoul Trading Item IL1014A, PIGGY Lotte Crispy Crunch Ice Cream Cone recall — FDA H-0191-2026
Undeclared peanut.
Class IFDA: TerminatedSeoul Trading, Inc.
VehicleNov 18, 2025
Sonata fuel system, gasoline recall — NHTSA campaign 25V796000
Hyundai Motor America (Hyundai) is recalling certain 2020-2023 Sonata vehicles. A damaged check valve can allow air to enter the fuel tank, causing it to expand and contact hot exhaust…
fuel system, gasolineHyundai Motor America
VehicleNov 14, 2025
Ford instrument cluster/panel recall — NHTSA campaign 25V788000
Ford Motor Company (Ford) is recalling certain 2025-2026 Bronco and Bronco Sport vehicles. The Instrument Panel Cluster (IPC) may fail at startup.
instrument cluster/panelFord Motor Company
VehicleNov 14, 2025
Ford electronic stability control (esc) recall — NHTSA campaign 25V787000
Ford Motor Company (Ford) is recalling certain 2025 Maverick and Escape vehicles. The cover for the electric brake booster's ECU may cause the printed circuit board to overheat and result…
electronic stability control (esc)Ford Motor Company
VehicleNov 12, 2025
Volkswagen Group of anchorage recall — NHTSA campaign 25V777000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2025 Audi RS Q8, Audi Q8, Audi Q7, and Audi SQ8 vehicles. The driver and front passenger seat belt buckles may be missing…
anchorageVolkswagen Group of America, Inc.
Medical DeviceNov 12, 2025
Integra LifeSciences TruDi Navigation System - Multi Instrument Adapter recall — FDA Z-0420-2026
It was determined that when the navigation system is configured with specific revision combinations of the Multi Instrument Adapter together with the Patient Tracker the system may not meet…
Class IIFDA: OngoingIntegra LifeSciences Corp. (NeuroSciences)
Medical DeviceNov 12, 2025
Beckman Coulter SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent, REF: 969706 recall — FDA Z-0441-2026
Beckman Coulter has identified that there is an increased probability Synchron Systems Direct LDL Cholesterol (LDLD REF 969706) reagent lot M404166 may generate false high results. The…
Class IIFDA: OngoingBeckman Coulter Inc.
Medical DeviceNov 12, 2025
Beckman Coulter UniCel DxI 800, Part Numbers: 973100, A71456 recall — FDA Z-0429-2026
An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceNov 12, 2025
Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated recall — FDA Z-0427-2026
Insulin pump includes a vibration motor that gives tactile feedback for any alerts, alarms, or malfunctions. Pump may exhibit false vibration motor failure due to a software issue causing…
Class IFDA: OngoingTandem Diabetes Care, Inc.
Medical DeviceNov 12, 2025
Integra LifeSciences CODMAN Disposable Perforator 9mm recall — FDA Z-0374-2026
Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution.
Class IFDA: OngoingIntegra LifeSciences Corp. (NeuroSciences)
Medical DeviceNov 12, 2025
Leksell Vantage Stereotactic System Software Version: n/a Product Description: The Intended recall — FDA Z-0433-2026
Due to increased risk that paint flakes from the engravings may separate from the device and there is the possibility that the flake may inadvertently enter the wound
Class IIFDA: OngoingElekta, Inc.
Medical DeviceNov 12, 2025
B-K Medical A/S bk3500 Ultrasound System w/battery recall — FDA Z-0439-2026
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life…
Class IIFDA: OngoingB-K Medical A/S
Medical DeviceNov 12, 2025
Sentinel V11 recall — FDA Z-0416-2026
Due to two distinct issues: 1. During patient admission, patient demographic fields may default to those of a previously viewed patient. 2. Systems configured with Resting/Rhythm ECG…
Class IIFDA: OngoingSpacelabs Healthcare, Ltd.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
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 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories