Safety Recall Directory
Browse and filter the latest official safety alerts globally.
Showing 24 of 74,116 results
Medical Device
FDA Devices
FDA DevicesATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.
Alphatec Spine, Inc.
FDA DevicesClass II
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.
Due a design issue where the navigated array connection geometry is incorrect.
Feb 18, 2026Alphatec Spine, Inc.
Medical DeviceFDA Devices
FDA Devicesda Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45
Intuitive Surgical, Inc.
FDA DevicesClass II
da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45
Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception) but 2D maintained, or loss of both displays-complete visualization loss, without fault, instruments remain active, could lead to instrument contact with tissue, resulting in injury/bleeding; may require alternate surgical modality.
Feb 18, 2026Intuitive Surgical, Inc.
Medical DeviceFDA Devices
FDA DevicesMedline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT, Kit SKU DT22710; 2) LINE KIT, Kit SKU DYNDA1857A; 3) PICC REMOVAL KIT, Kit SKU DYNDC1978A; 4) PORT ACCESS TRAY, Kit SKU DYNDC2367; 5) NICU CENTRAL LINE TRAY, Kit SKU DYNDC2407B; 6) CVC DRESSING CHANGE W/ TEG CHG, Kit SKU DYNDC3222A; 7) PICC PROCEDURE PACK, Kit SKU DYNJ59067A; 8) PICC PROCEDURE PACK, Kit SKU PHS950205004B.
Medline Industries, LP
FDA DevicesClass II
Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT, Kit SKU DT22710; 2) LINE KIT, Kit SKU DYNDA1857A; 3) PICC REMOVAL KIT, Kit SKU DYNDC1978A; 4) PORT ACCESS TRAY, Kit SKU DYNDC2367; 5) NICU CENTRAL LINE TRAY, Kit SKU DYNDC2407B; 6) CVC DRESSING CHANGE W/ TEG CHG, Kit SKU DYNDC3222A; 7) PICC PROCEDURE PACK, Kit SKU DYNJ59067A; 8) PICC PROCEDURE PACK, Kit SKU PHS950205004B.
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.
Feb 18, 2026Medline Industries, LP
Medical DeviceFDA Devices
FDA DevicesATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.
Alphatec Spine, Inc.
FDA DevicesClass II
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use instruments designed to function with the Medtronic StealthStation System and NavLock Tracker.
Due a design issue where the navigated array connection geometry is incorrect.
Feb 18, 2026Alphatec Spine, Inc.
Medical DeviceFDA Devices
FDA DevicesMedline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108
Medline Industries, LP
FDA DevicesClass II
Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108
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.
Feb 18, 2026Medline Industries, LP
Safety Alert
Health Canada
Health CanadaTrilogy EVO and EV300
Medical devices
Health CanadaType I
Trilogy EVO and EV300
Device compatibility
Feb 18, 2026Medical devices
Safety AlertHealth Canada
Health CanadaKlask 4 recalled due to ingestion hazard
Consumer product safety
Health CanadaGeneral Alert
Klask 4 recalled due to ingestion hazard
Ingestion hazard
Feb 18, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaSunshade and alternating blind by Stores d’aujourd’hui Gatineau Inc. recalled due to strangulation and choking hazards
Consumer product safety
Health CanadaGeneral Alert
Sunshade and alternating blind by Stores d’aujourd’hui Gatineau Inc. recalled due to strangulation and choking hazards
Choking hazard - Strangulation hazard
Feb 18, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaBoneless Chicken Thighs recalled due to semicarbazide
CFIA
Health CanadaClass 3
Boneless Chicken Thighs recalled due to semicarbazide
Contamination
Feb 18, 2026CFIA
Safety AlertHealth Canada
Health CanadaRaha Generator Shield
Medical devices
Health CanadaType II
Raha Generator Shield
Performance
Feb 18, 2026Medical devices
Safety AlertHealth Canada
Health CanadaKiestra ReadA
Medical devices
Health CanadaType II
Kiestra ReadA
Performance
Feb 18, 2026Medical devices
Safety AlertHealth Canada
Health CanadaUniversal Viewer - System Feature
Medical devices
Health CanadaType II
Universal Viewer - System Feature
Performance
Feb 18, 2026Medical devices
Safety AlertHealth Canada
Health CanadaLeksell Gamma Knives
Medical devices
Health CanadaType II
Leksell Gamma Knives
Performance
Feb 18, 2026Medical devices
Safety AlertHealth Canada
Health CanadaCEFAZOLIN FOR INJECTION : Vials may be underfilled in the affected lot.
Drugs and health products
Health CanadaType I
CEFAZOLIN FOR INJECTION : Vials may be underfilled in the affected lot.
Product quality
Feb 18, 2026Drugs and health products
Safety AlertHealth Canada
Health CanadaTeva-Indomethacin: Out of specification
Drugs and health products
Health CanadaType II
Teva-Indomethacin: Out of specification
Product quality
Feb 18, 2026Drugs and health products
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026062 - DUCATI
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026062 - DUCATI
Brakes
Feb 18, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026052 - MERCEDES-BENZ
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026052 - MERCEDES-BENZ
High Voltage
Feb 18, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2025030 - DUCATI
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2025030 - DUCATI
Brakes
Feb 18, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026048 - BMW
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026048 - BMW
Lights And Instruments
Feb 18, 2026TC
Medical DeviceFDA Devices
FDA DevicesReprocessed St. Jude Supreme and Response Diagnostic Electrophysiology Catheters: St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 2-5-2mm 401211RH 401222RH 401223RH 401226RH 401227RH 401260RH 401261RH 401306RH 401309RH 401312RH 401430RH 401433RH 401435RH 401441RH 401442RH 401443RH 401448RH 401449RH 401450RH 401451RH 401474RH 401860RH 401877RH 401878RH 401890RH 401891RH 401994RH; St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 5-5-5mm 402012RH; St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 5mm 402004RH; St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 6 Elec. 2-5-2mm 402010RH; St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 6 Elec. 5-5-5mm 402008RH 402009RH
Medline Industries, LP
FDA DevicesClass I
Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology Catheters: St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 2-5-2mm 401211RH 401222RH 401223RH 401226RH 401227RH 401260RH 401261RH 401306RH 401309RH 401312RH 401430RH 401433RH 401435RH 401441RH 401442RH 401443RH 401448RH 401449RH 401450RH 401451RH 401474RH 401860RH 401877RH 401878RH 401890RH 401891RH 401994RH; St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 5-5-5mm 402012RH; St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4 Elec. 5mm 402004RH; St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 6 Elec. 2-5-2mm 402010RH; St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 6 Elec. 5-5-5mm 402008RH 402009RH
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
Feb 18, 2026Medline Industries, LP
PharmaceuticalFDA Drugs
FDA DrugsPro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11
Pro Numb Tattoo Numbing Spray LLC
FDA DrugsClass II
Pro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-11
cGMP deviations
Feb 18, 2026Pro Numb Tattoo Numbing Spray LLC
Food & BeverageFDA Food
FDA FoodSonic Tots, item number SON00543. Frozen potato product is packaged in clear unlabeled poly bags (6/5 lb), Net Wt 30 lbs (13.61 kg)/ case. UPC 0 00 72714 00543 5. Manufactured By: McCain Foods USA Inc. Oakbrook Terrace, IL.
McCain Foods USA Inc
FDA FoodClass II
Sonic Tots, item number SON00543. Frozen potato product is packaged in clear unlabeled poly bags (6/5 lb), Net Wt 30 lbs (13.61 kg)/ case. UPC 0 00 72714 00543 5. Manufactured By: McCain Foods USA Inc. Oakbrook Terrace, IL.
Foreign material (small hard plastic fragments).
Feb 18, 2026McCain Foods USA Inc
PharmaceuticalFDA Drugs
FDA DrugsTestosterone, 18.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1018-32.
F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II
Testosterone, 18.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1018-32.
Presence of Foreign substance - potential presence of metal particulate matter
Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
Food & BeverageFDA Food
FDA FoodKarison brand ALSI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar Flax Seeds, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00251 2; 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 Foods & Snacks, Inc.
FDA FoodClass II
Karison brand ALSI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar Flax Seeds, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00251 2; 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.
Feb 18, 2026Karison Foods & Snacks, Inc.