Recalls in Michigan (page 27)
3990 recalls.
- VACUUM BAG SU LARGE recall (Milestone S.R.L.)
Medical deviceClass IIReported May 6, 2026 · There is a possibility of reagent leakage from the specimen container. - Mesh Style Tip Protectors CSW-03-2.0 Open-end style CSW-04-4.0 Closed-end style recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported May 6, 2026 · Product does not have FDA clearance. - American Honda Motor Recalls Off-Road Motorcycles Due to Risk of Serious Injury or Death Due to Crash Hazard
Consumer productReported May 1, 2026 · The handlebar's clamp can unexpectedly cause the handlebar to rotate, posing a risk of serious injury or death due to a crash hazard. - Build-A-Bear Workshop Recalls Heartwarming Hugs Bears Due to Risk of Serious Injury or Death from Choking Hazard to Children
Consumer productReported May 1, 2026 · The zipper slider on the side pouch can detach, posing a risk of serious injury or death from choking hazard to children. - CBC Group Recalls Stephan Baby Boo Bunnie and Friends Children's Toys Due to Risk of Serious Injury from Choking and Laceration Hazards
Consumer productReported May 1, 2026 · The toys' plastic cube can break into small parts or sharp edges, posing a risk of serious injury from choking and laceration hazards. - Bayer Recalls 6 mL Size Afrin Original Nasal Spray Bottles Due to Risk of Serious Injury or Illness from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported May 1, 2026 · The 6 mL nasal sprays contain an imidazoline, which must be in child-resistant packaging or meet the labeling requirements for non-complying packaging, as... - Qumeney Bicycle Light Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by Smfanlus
Consumer productReported May 1, 2026 · The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries... - Acer America Corporation Recalls Two-Wheeled Folding Electric Due to Risk of Injury from Fall Hazard
Consumer productReported May 1, 2026 · A loose screw can cause the front tube to fold down unexpectedly, posing a risk of injury from a fall hazard. - Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by DGIVOVO US
Consumer productReported May 1, 2026 · The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution... - Earthtec Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Manufactured by Tonyidea
Consumer productReported May 1, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and... - Residential Elevators Recalls Elevator StrikeLock Hoistway Door Locking Device Due to Risk of Serious Injury or Death from Fall and Injury Hazards
Consumer productReported May 1, 2026 · The elevator's StrikeLock hoistway door locking device can allow the elevator cab to move with a landing door open, posing a risk of serious injury or death... - Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Imported by Hepo Care Medical Equipment Online
Consumer productReported May 1, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by UHOMEPRO
Consumer productReported May 1, 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... - Malker Bicycle Light Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by MalkerDirect
Consumer productReported May 1, 2026 · The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries... - Segmart 4-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Storage Units; Sold on Walmart.com by SOFT
Consumer productReported May 1, 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... - Alliance Chemical Recalls 1-K Kerosene Heater Fluid Containers Due to Risk of Serious Injury or Death from Flash Fire, Burn and Child Poisoning; Violates Mandatory Standards for Portable Fuel Containers
Consumer productReported May 1, 2026 · The pre-filled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under... - Thermos Recalls 8.2 Million Stainless King Food Jars and Bottles Due to Serious Impact Injury and Laceration Hazards
Consumer productReported May 1, 2026 · If perishable food or beverages are stored in the container for an extended period of time, the stopper can forcefully eject when opened, which can result in... - EL MEXICANO agua fresca de horchata Instant Horchata Drink recall (Marquez Brothers International, Inc.)
FoodClass IIReported April 29, 2026 · Undeclared milk. - EL MEXICANO horchata casera Instant Horchata Drink recall (Marquez Brothers International, Inc.)
FoodClass IIReported April 29, 2026 · Undeclared milk. - Bulk Horchata Powder 3951 recall (Marquez Brothers International, Inc.)
FoodClass IIReported April 29, 2026 · Undeclared milk. - Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator recall (Diversatek Healthcare)
Medical deviceClass IIReported April 29, 2026 · The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each... - Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator recall (Diversatek Healthcare)
Medical deviceClass IIReported April 29, 2026 · The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each... - Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator recall (Diversatek Healthcare)
Medical deviceClass IIReported April 29, 2026 · The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each... - Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator recall (Diversatek Healthcare)
Medical deviceClass IIReported April 29, 2026 · The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each... - Oxoid Agglutinating Sera recall (Remel Europe Ltd.)
Medical deviceClass IIReported April 29, 2026 · Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a... - Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr.... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - ARROW recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - FLEXTIP PLUS EPIDURAL CATHETER recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured - CUSA Clarity C7000 Console recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported April 29, 2026 · Software issue that renders the touch screen unresponsive. - Claravis recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 29, 2026 · Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin - LACTATED RINGER'S IRRIGATION recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - 0.9 % SODIUM CHLORIDE IRRIGATION recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - DEXTROSE INJECTION USP recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - Sterile Water for Injection USP recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - Omega-3-Acid recall (The Harvard Drug Group LLC)
DrugClass IIReported April 29, 2026 · Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells. - Premier recall (Premier Dental Products Co)
DrugClass IIIReported April 29, 2026 · Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14).... - FRESHKOTE LUBRICANT EYEDROPS recall (Harrow Eye LLC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility - Furosemide Tablets recall (Leading Pharma, LLC)
DrugClass IIReported April 29, 2026 · CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit. - Pantoprazole Sodium recall (Hetero Labs Limited (Unit V))
DrugClass IIReported April 29, 2026 · Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots." - LSL Healthcare Wound Closure Tray recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - Sequencing Agent SEQ0067 recall (Foundation Medicine, Inc.)
Medical deviceClass IIReported April 29, 2026 · Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants - Flamingo Funnel Large recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Flamingo Funnel Medium recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Flamingo Funnel Small recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Access Total T4 Calibrator recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported April 29, 2026 · Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71 recall (Micro-X Ltd.)
Medical deviceClass IIReported April 29, 2026 · X-Ray generator may malfunction resulting in the X-Ray being inoperable. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · XXX - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft... recall (XTANT Medical Holdings, Inc)
Medical deviceClass IIReported April 29, 2026 · Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years. - Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog... recall (Davol, Inc.)
Medical deviceClass IIReported April 29, 2026 · Potential for product to contain foreign matter, confirmed to be inspect fragments. - LeadCare Ultra Blood Lead Test Kit recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - LeadCare¿ Plus Blood Lead Test Kit recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - (1)(2) LeadCare¿ II Blood Lead Test Kit, (3)LeadCare¿ II 5X Blood Lead Test Kit, recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the...