Recalls in North Dakota (page 35)
3825 recalls.
- 25GA Subretinal Injection Cannula VS0220.25 recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive VS0740.23 ... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Laser Probe OS4... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Focalyx Fusion recall (Focalyx Technologies, LLC.)
Medical deviceClass IIReported February 11, 2026 · Software device that is an accessory for image-guided interventional and diagnostic procedures involving prostate has accessories that may not function... - NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT Vessel... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT... recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 11, 2026 · To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance. - TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE recall (Tornier, Inc)
Medical deviceClass IIReported February 11, 2026 · A specific lot of screws is incorrectly labeled. Screws are labeled as 5.0mmx18mm but actual screws are 5.00mmx14mm. If mismatch is detected during surgery... - VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B recall (Biomerieux Inc)
Medical deviceClass IIReported February 11, 2026 · Potential risk of Quality Control failures and/or false resistant antibiotic results when testing isolates of Enterobacterales/Enterobacteriaceae species... - CellMek SPS Sample Preparation System recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported February 11, 2026 · Sample preparation system designed to automate staining, lysing, cell washing has a software error that causes samples to be dispensed close to or touching... - PRISMAFLEX TPE2000 SET recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - PRISMAFLEX HF1000 SET recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - PRISMAFLEX HF1000 SET recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - PRISMAFLEX M150 SET recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - PRIMSAFLEX M100 SET recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - OXIRIS SET recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - PRISMAFLEX ST150 SET US recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - PRISMAFLEX ST100 SET US recall (VANTIVE US HEALTHCARE LLC)
Medical deviceClass IIReported February 11, 2026 · There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. - *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm recall (Boston Scientific Corporation)
Medical deviceClass IReported February 11, 2026 · Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is... - *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm recall (Boston Scientific Corporation)
Medical deviceClass IReported February 11, 2026 · Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is... - HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm recall (Boston Scientific Corporation)
Medical deviceClass IReported February 11, 2026 · Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is... - AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm recall (Boston Scientific Corporation)
Medical deviceClass IReported February 11, 2026 · Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is... - AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm recall (Boston Scientific Corporation)
Medical deviceClass IReported February 11, 2026 · Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is... - AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm recall (Boston Scientific Corporation)
Medical deviceClass IReported February 11, 2026 · Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is... - Andy & Evan Recalls Children's Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear
Consumer productReported February 6, 2026 · The recalled children's pajamas violate the mandatory flammability standard for children's sleepwear, posing a risk of serious burn injuries or death. - EnHomee 10-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported February 6, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Cobelae Busy Books Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates Small Parts Ban; Sold on Amazon by Flyindream
Consumer productReported February 6, 2026 · The toy books violate the small parts ban because the beads can loosen and detach from the product, posing a deadly choking hazard. - Clark Associates Recalls Lancaster Table & Seating Powder-Coated Aluminum Outdoor Restaurant Chairs and Barstools Due to Fall Hazard
Consumer productReported February 6, 2026 · The legs of the chairs and barstools can bend or break while the chair is in use, posing a fall hazard. - Scepter Fuel Containers Recalled Due to Risk of Serious Injury or Death from Flash Fire, Burn and Child Poisoning; Violates Mandatory Standards for Portable Fuel Containers; Imported by Mameix Retail
Consumer productReported February 6, 2026 · The recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the... - YITA Recalls Multiple Brands of Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported February 6, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Aterian Recalls PurSteam Elite Travel Steamers and Mighty Lil Steamers Due to Risk of Serious Burn Injury
Consumer productReported February 6, 2026 · The steamers can expel hot water from the steam nozzle during use, posing a serious burn hazard to consumers. - Dresbe LED Christmas Headbands Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
Consumer productReported February 6, 2026 · The recalled headbands violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries in the... - Fixwal 7-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported February 6, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Furnulem 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported February 6, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Kitosun Submersible LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
Consumer productReported February 6, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin... - GM Gumili Wintergreen Essential Oil Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Gumili Beauty
Consumer productReported February 6, 2026 · The essential oil contains methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The... - Organic Zing Birch Essential Oil Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Linkers
Consumer productReported February 6, 2026 · The essential oil bottles contain methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The... - Little Cow Company Recalls 9 oz Candles in Glass Jars Due to Fire, Burn and Laceration Hazards
Consumer productReported February 6, 2026 · The glass jar holding the candle can crack or break during use, posing fire, burn and laceration hazards. - Lola Plus The Boys Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Strangulation Hazard; Violates Federal Rule for Children's Upper Outerwear
Consumer productReported February 6, 2026 · The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children due to the strangulation hazard. The clothes... - Semfri Children's Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported February 6, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional... - Shintenchi 6-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported February 6, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - Zan International Trading Recalls Lotus Joy Sweet Birch Essential Oil Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported February 6, 2026 · The essential oil bottles contain methyl salicylate, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act (PPPA). The... - Conductivity Standard Solution Catalog/Model Numbers: 10001 recall (NIPRO Technical Services, Inc.)
Medical deviceClass IIReported February 4, 2026 · due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values... - a.) Live it Up brand Super Greens recall (SUPERFOODS, INC.)
FoodClass IReported February 4, 2026 · Products may be contaminated with Salmonella Typhimurium - Live it Up brand Super Greens recall (SUPERFOODS, INC.)
FoodClass IReported February 4, 2026 · Products may be contaminated with Salmonella Typhimurium - Glycopyrrolate Oral Solution recall (NOVADOZ PHARMACEUTICALS LLC)
DrugClass IIIReported February 4, 2026 · Failed Impurities/Degradation Specifications - methylprednisolone tablets recall (Greenstone Llc)
DrugClass IIReported February 4, 2026 · Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information... - parodontax recall (Haleon US Holdings LLC)
DrugClass IIIReported February 4, 2026 · Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles. - Sterile Water for Irrigation recall (Baxter Healthcare Corporation)
DrugClass IIReported February 4, 2026 · Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution - BEAR Implant. Model Number: 1000. recall (Miach Orthopaedics)
Medical deviceClass IIReported February 4, 2026 · Incorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will also be... - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported February 4, 2026 · BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators. - Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23 recall (LimFlow, Inc.)
Medical deviceClass IIReported February 4, 2026 · Incorrect expiration date - SmartPath to dStream for XR and 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - SmartPath to dStream for 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Upgrade to MR 7700. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - MR 7700. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Elition X. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Elition S. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Ambition X. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia Ambition S. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 3.0T CX. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Ingenia 1.5T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Evolution Upgrade 3.0T. Product Code recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Evolution Upgrade 1.5T. Product Codes recall (Philips North America)
Medical deviceClass IIReported February 4, 2026 · The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS). - Chest Drainage Units and Accessories: Product Code Description 1.... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported February 4, 2026 · The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older.... - Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: 1) CATH LAB PACEMAKER PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2 recall (Medline Industries, LP)
Medical deviceClass IIReported February 4, 2026 · Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during... - PREGNANCY TEST 24CT recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Toothbrushes recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Feminine hygiene products recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Condoms recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Bandages and first aid kits: FIRST AID KIT 24/42PC recall (GOLD STAR DISTRIBUTION INC)
Medical deviceClass IIReported February 4, 2026 · Potential exposure of rodents and rodent activity in the distribution center. - Alphenix INFX-8000V recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000H recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000F recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Alphenix INFX-8000C recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported February 4, 2026 · It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray... - Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 4, 2026 · Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a... - Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported February 4, 2026 · Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a... - AlternatiV+ Screw-In Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - AlternatiV+ Max Knotless Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Push-In Suture Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Knotless Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. - Genesis Dual Thread Screw-In Anchor recall (Aju Pharm Co., Ltd.)
Medical deviceClass IIReported February 4, 2026 · Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.