Safety Recall Directory
Browse and filter the latest official safety alerts globally.
FDA DevicesAzurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
Health CanadaTrilogy EVO and EV300
Trilogy EVO and EV300
Device compatibility
Health CanadaKlask 4 recalled due to ingestion hazard
Klask 4 recalled due to ingestion hazard
Ingestion hazard
Health CanadaSunshade and alternating blind by Stores d’aujourd’hui Gatineau Inc. recalled due to strangulation and choking hazards
Sunshade and alternating blind by Stores d’aujourd’hui Gatineau Inc. recalled due to strangulation and choking hazards
Choking hazard - Strangulation hazard
Health CanadaTransport Canada Recall - 2026062 - DUCATI
Transport Canada Recall - 2026062 - DUCATI
Brakes
Health CanadaBoneless Chicken Thighs recalled due to semicarbazide
Boneless Chicken Thighs recalled due to semicarbazide
Contamination
Health CanadaRaha Generator Shield
Raha Generator Shield
Performance
Health CanadaKiestra ReadA
Kiestra ReadA
Performance
Health CanadaTransport Canada Recall - 2026052 - MERCEDES-BENZ
Transport Canada Recall - 2026052 - MERCEDES-BENZ
High Voltage
Health CanadaUniversal Viewer - System Feature
Universal Viewer - System Feature
Performance
Health CanadaLeksell Gamma Knives
Leksell Gamma Knives
Performance
Health CanadaTeva-Indomethacin: Out of specification
Teva-Indomethacin: Out of specification
Product quality
Health CanadaCEFAZOLIN FOR INJECTION : Vials may be underfilled in the affected lot.
CEFAZOLIN FOR INJECTION : Vials may be underfilled in the affected lot.
Product quality
Health CanadaTransport Canada Recall - 2025030 - DUCATI
Transport Canada Recall - 2025030 - DUCATI
Brakes
Health CanadaTransport Canada Recall - 2026048 - BMW
Transport Canada Recall - 2026048 - BMW
Lights And Instruments
FDA FoodKarison brand PUNJABI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00215 4; Distributed By: Karison Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Karison brand PUNJABI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00215 4; Distributed By: Karison Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Product contains milk, which is undeclared in the ingredient statement.
FDA FoodSodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc., West Palm Beach, FL 33041
Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc., West Palm Beach, FL 33041
Undeclared Aspartame
FDA DevicesMedline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
FDA DevicesMedline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
FDA DrugsTestosterone, 25.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1025-32.
Testosterone, 25.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1025-32.
Presence of Foreign substance - potential presence of metal particulate matter
FDA DevicesMedline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit
Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit
A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
FDA DevicesAzurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
FDA DevicesAzurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X
Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
Health CanadaMaison Luce brand Sérum fortifiant Cils & Sourcils recalled due to chemical hazard
Maison Luce brand Sérum fortifiant Cils & Sourcils recalled due to chemical hazard
Chemical hazard