Browse recalls
Year: 2024
- 2024-03-29 · RappelConso (France)volontaire (sans arrêté préfectoral)
tentation patissière 0% - 2024-03-28 · US CPSC
Berkley Jensen Citronella 72-inch Tiki Torches - 2024-03-28 · US CPSC
Forias Pack and Play Mattresses - 2024-03-28 · US CPSC
Model Year 2022-2023 Snowmobiles equipped with PATRIOT BOOST Engines - 2024-03-28 · US CPSC
Purefog High Density Natural Fog Juice Liquids - 2024-03-28 · US CPSC
Magnetic Beads HIGH POWER 5mm - 2024-03-28 · Transport Canada
CHRYSLER GRAND CARAVAN 2024 - 2024-03-28 · Transport Canada
JEEP CHEROKEE 2022 - 2024-03-28 · Transport Canada
MICRO BIRD G5 COMMERCIAL BUS 2023-2024 - 2024-03-28 · Transport Canada
MICRO BIRD G5 SCHOOL BUS 2021-2024 - 2024-03-28 · Transport Canada
KAWASAKI NINJA ZX-4 2023-2024 - 2024-03-28 · NHTSA (USA)
JEEP CHEROKEE (2022) - 2024-03-28 · NHTSA (USA)
CHRYSLER VOYAGER (2024) - 2024-03-27 · US FDA — Medical DevicesClass II
Newport s N-LHP-928(j) units if sold as a laser head/power supply set, and N5-LPL-944-080 and N6-LPL-944-080 if sold as - 2024-03-27 · Transport Canada
MACK LR 2024-2025 - 2024-03-27 · Transport Canada
CRUISER RV STRYKER 2023-2024 - 2024-03-27 · Transport Canada
HEARTLAND NORTH TRAIL 2023-2024 - 2024-03-27 · Transport Canada
KENWORTH T680 2025 - 2024-03-27 · NHTSA (USA)
HEARTLAND NORTH TRAIL (2024) - 2024-03-27 · NHTSA (USA)
PETERBILT 567 (2025) - 2024-03-27 · OECD GlobalRecalls — KR
Food-waste disposal unit for household - 2024-03-27 · DVSA (UK)Safety recall
LAND ROVER RANGE ROVER SPORT — AJ20-D6 Fuel Injector Clamp Cracked - 2024-03-27 · NHTSA (USA)
KEYSTONE MONTANA (2021) - 2024-03-26 · US FDA — Medical DevicesClass I
BiPAP V30 Auto Ventilator, Part Number 1111178 - 2024-03-26 · US FDA — Medical DevicesClass I
BiPAP A40 Ventilators: BiPAP A40, Part Numbers 1111169 (US and OUS) and (OUS ONLY)1111170 1111171 1111173 11111 - 2024-03-26 · US FDA — Medical DevicesClass I
BiPAP A30 Ventilator, Part Number 1111143 (US and OUS) OUS Only: Part Numbers 1111144 1111145 1111147 1111148 11 - 2024-03-26 · ACCC (Australia)Product Recall
Digital Notepad and Infinity Colour Pad - 2024-03-26 · ACCC (Australia)Product Recall
Various Novelty Lighting Products - 2024-03-26 · OECD GlobalRecalls — KR
Zero Turn Lawn Mowers - 2024-03-26 · DVSA (UK)Safety recall
FORD KUGA — 24S16 - Kuga - PCM Programming and Drain Tube Installation - 2024-03-25 · Food Standards Agency (UK)Product Recall Information Notice
The Best Taleggio - 2024-03-25 · Transport Canada
FORD MAVERICK 2023 - 2024-03-23 · Transport Canada
FORD MUSTANG 2024 - 2024-03-22 · Transport Canada
KIA TELLURIDE 2020-2024 - 2024-03-22 · Transport Canada
AUDI E-TRON GT 2022-2024 - 2024-03-22 · Transport Canada
SUBARU OUTBACK 2020-2022 - 2024-03-22 · ACCC (Australia)Product Recall
Various novelty products - 2024-03-22 · NHTSA (USA)
SUBARU OUTBACK (2020) - 2024-03-21 · US CPSC
BRS and BULin Liquid Fuel Bottles - 2024-03-21 · US CPSC
Crown Aruba IV (AWR Series) gas-fired hot water boilers - 2024-03-21 · US CPSC
Sneaker Basel Double Magnetic Levitation Displays - 2024-03-21 · US CPSC
Fisher-Price Little People Mickey and Friends Figures - 2024-03-21 · US CPSC
Metallic Mugs included in 2023 Holiday Starbucks-branded Gift Sets - 2024-03-21 · US CPSC
Ravin R500 Model Crossbows - 2024-03-21 · US CPSC
Happiness USA Liquid Rolling Candy - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR6 (5PK), REF H74908526042; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR1 (5PK), REF H74908526842; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 (5PK), REF H74908526022; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IM (5PK), REF H749085262012; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 125CM (5PK), REF H749085262352; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4 (5PK), REF H74908526222; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265022; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (5PK), REF H74908526512; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 (SGL), REF H74908526031; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS4 (5PK), REF H74908526575A2; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 MOD (5PK), REF H74908526052; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (SGL), REF H749085263011; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085265002; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 (5PK), REF H7490852624; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL3 (5PK), REF H749085261002; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL3 (5PK)REF H7490852620A2; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR2 (5PK), REF H74908526862; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR MOD (5PK), REF H74908526892; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL1 (5PK), REF H74908526962; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3.5 (5PK), REF H74908526574A2; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS2.5 (5PK), REF H74908526572A2; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO TIG4 (5PK), REF H749085262502; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (SGL), REF H749085263001; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4.5 (5PK), REF H74908526232; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO KIMNY (5PK), REF H749085261802; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO LCB (5PK), REF H749085261952; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IMT (5PK), REF H749085262022; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 125CM (5PK), REF H749085262252; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass II
Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models: Artis zee floor- 10094135 Artis zee ceiling- 1 - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 (5PK), REF H74908526032; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 155 (5PKX3), REF H749085263022; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL2 (5PK), REF H74908526982; cardiac catheter - 2024-03-21 · US FDA — Medical DevicesClass I
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749085263012; cardiac catheter - 2024-03-21 · Transport Canada
JAYCO SWIFT 2023-2024 - 2024-03-21 · Transport Canada
VICINITY VMC 1200 2023-2024 - 2024-03-21 · Transport Canada
BMW R1300 GS 2024 - 2024-03-21 · Transport Canada
AMP TIRES MUD TERRAIN ATTACK M/T 2019-2024 - 2024-03-21 · ACCC (Australia)Product Recall
Revell Reading Glasses with LED Light – sold at Dimmeys - 2024-03-21 · ACCC (Australia)Product Recall
Various novelty items - 2024-03-21 · RappelConso (France)volontaire (sans arrêté préfectoral)
salade d'algues à la japonaise - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Sterile- Indicated - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and sta - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 16 Holes, 236 MM, Sterile- Indicate - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP Distal Lateral Fibular Plate, Left, 14 Holes, 210 MM, Sterile- Indicated for temporary internal fixation and stabil - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 6 Holes, 106 MM, Sterile- Indicat - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP Distal Lateral Fibular Plate, Right, 8 Holes, 132 MM, Nonsterile- Indicated for temporary internal fixation and sta - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP Distal Lateral Fibular Plate, Left, 6 Holes, 106 MM, Nonsterile- Indicated for temporary internal fixation and stab - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Sterile- Indicated - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 MM, Sterile- Indicat - 2024-03-20 · US FDA — Medical DevicesClass II
Alinity m System, Part Number: 08N53-002 - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Sterile- Indicated - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Nonsterile- Indicated for temporary internal fixation and stabi - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 12 Holes, 184 MM, Sterile- Indicat - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 10 Holes, 158 MM, Sterile- Indicat