Archive
All indexed recalls — page 159 of 192
- 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 · Health Canada Consumer Product Safety
Fisher-Price Little People Mickey and Friends figure packs - 2024-03-21 · Health Canada Consumer Product Safety
Indigenous Collection Ceramic Plates by Canadian Art Prints - 2024-03-21 · Health Canada Consumer Product Safety
Elin Dessert Plates sold by Anthropologie - 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 TERRAIN PRO A/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 · Transport Canada
SUV recalled by HONDA - 2024-03-20 · Transport Canada
Truck - Med. & H.D. recalled by ROSENBAUER - 2024-03-20 · Transport Canada
SUV recalled by FIAT CHRYSLER AUTOMOBILES - 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 - 2024-03-20 · US FDA — Medical DevicesClass II
ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Sterile- Indicate - 2024-03-20 · Transport Canada
PORSCHE TAYCAN TURBO 2020-2023 - 2024-03-20 · Transport Canada
PORSCHE TAYCAN 2020-2024 - 2024-03-20 · Transport Canada
POLARIS TITAN 2024 - 2024-03-20 · NHTSA (USA)
KENWORTH T880 (2025) - 2024-03-20 · NHTSA (USA)
PORSCHE TAYCAN (2024) - 2024-03-20 · DVSA (UK)Safety recall
PORSCHE PANAMERA — ARA1 Replacing front right wheel carrier - 2024-03-20 · NHTSA (USA)
PORSCHE TAYCAN 4S (2020) - 2024-03-19 · Transport Canada
Truck - Med. & H.D. recalled by DAIMLER TRUCK NORTH AMERICA - 2024-03-19 · Transport Canada
DODGE HORNET 2023-2024 - 2024-03-19 · Transport Canada
JAYCO SOLSTICE 2023-2024 - 2024-03-19 · OPSS (UK)Product Safety Report
Front pharmaceutical tydineal steroid cream - 2024-03-19 · OPSS (UK)Product Safety Report
El paradis cosmetic nature secrete a lhuile dargan - 2024-03-19 · OPSS (UK)Product Safety Report
Irodis bb clear skin lightening cream - 2024-03-19 · OPSS (UK)Product Safety Report
Sivop parfums and cosmetiques clair liss lightening body cream - 2024-03-19 · OPSS (UK)Product Safety Report
Skin gard lightening lotion - 2024-03-19 · OPSS (UK)Product Safety Report
Uniparco pure white cosmetics gold glowing - 2024-03-19 · OPSS (UK)Product Safety Report
H cosmetiques ci labidjanaise cream - 2024-03-19 · OPSS (UK)Product Safety Report
Gandour light and natural carotone skin lightening cream - 2024-03-19 · OPSS (UK)Product Safety Report
White moon neutrotone steroid cream - 2024-03-19 · OPSS (UK)Product Safety Report
Ct cosmetics extra pure white gold glowing bsc black spot corrector - 2024-03-19 · OPSS (UK)Product Safety Report
Beneks fashion fair cream - 2024-03-19 · OPSS (UK)Product Safety Report
Vixa skineal steroid cream - 2024-03-19 · OPSS (UK)Product Safety Report
Esapharma movate steroid cream - 2024-03-19 · OPSS (UK)Product Safety Report
Fabrique par rodis white secret unifying complexion serum - 2024-03-19 · OPSS (UK)Product Safety Report
Wau wa eczema herbal cream - 2024-03-19 · OPSS (UK)Product Safety Report
Gdk akagni skin toning cream - 2024-03-19 · OPSS (UK)Product Safety Report
Pts packers and providers pvt surfaz sn triple action cream - 2024-03-19 · OPSS (UK)Product Safety Report
Bliss gvs pharma funbact a steroid cream - 2024-03-19 · OPSS (UK)Product Safety Report
Silver rose extra pearl beauty cream - 2024-03-19 · OPSS (UK)Product Safety Report
Caring chemistry body treat maxitoner - 2024-03-19 · OPSS (UK)Product Safety Report
White express lightening body lotion - 2024-03-19 · NHTSA (USA)
DODGE HORNET (2024) - 2024-03-19 · NHTSA (USA)
ENTEGRA EXPANSE (2023) - 2024-03-18 · US FDA — Medical DevicesClass II
GE Healthcare Allia IGS 7 OR, Interventional fluoroscopic x-ray systems - 2024-03-18 · US FDA — Medical DevicesClass II
LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the Li - 2024-03-18 · US FDA — Medical DevicesClass II
GE Healthcare Interact Discovery RT, Interventional fluoroscopic x-ray systems - 2024-03-18 · Transport Canada
Motorhome recalled by FOREST RIVER - 2024-03-18 · US FDA — Medical DevicesClass II
GE Healthcare Allia IGS 5 Pulse, Interventional fluoroscopic x-ray systems - 2024-03-18 · US FDA — Medical DevicesClass II
GE Healthcare Innova IGS 5, computed tomography x-ray system - 2024-03-18 · US FDA — Medical DevicesClass II
GE Healthcare Allia IGS 7, Interventional fluoroscopic x-ray systems - 2024-03-18 · DVSA (UK)Safety recall
BMW X3 — Replacing the Driver’s Airbag PSDI-5 - 2024-03-15 · Transport Canada
Bus recalled by NOVA BUS - 2024-03-15 · Health Canada Consumer Product Safety
Various Chemical Guys brand chemical products - 2024-03-15 · Transport Canada
Car recalled by KIA - 2024-03-15 · Transport Canada
Light Truck & Van recalled by TOYOTA - 2024-03-15 · Transport Canada
MERCEDES-BENZ GLE CLASS 2020-2024 - 2024-03-15 · Transport Canada
DYNAMAX ISATA 2024-2025 - 2024-03-15 · Transport Canada
KIA EV6 2022-2024