Medical device recalls (page 5)
2545 recalls.
- Achieva 3.0T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - Achieva 1.5T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - VITEK 2 AST-N461 TEST KIT recall (Biomerieux Inc)
Medical deviceClass IIReported September 30, 2026 · The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe... - Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS... recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush.... - Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK... recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush.... - SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head recall (SEASPINE ORTHOPEDICS CORPORATION)
Medical deviceClass IIReported September 30, 2026 · The proximal thread depth of the spinal device is out of design specification. - CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 30, 2026 · Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed. - PowerLED 300 Concealed Lighting System recall (Maquet SAS)
Medical deviceClass IIReported September 30, 2026 · The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury. - REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post... recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - REF:HF2PC9 HomeFill Oxygen System recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - Midmark IQvitals Zone recall (Midmark Corporation)
Medical deviceClass IIReported September 30, 2026 · A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. - Midmark IQvitals Zone recall (Midmark Corporation)
Medical deviceClass IIReported September 30, 2026 · A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. - Midmark IQvitals Zone recall (Midmark Corporation)
Medical deviceClass IIReported September 30, 2026 · A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. - Midmark IQvitals Zone recall (Midmark Corporation)
Medical deviceClass IIReported September 30, 2026 · A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. - Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for the inflation chart label affixed to the shaft of the device to be incorrect and indicate a balloon diameter of 18, 19, or 20 mm, - Brand Name: Heidelberg Engineering GmbH Product Name: SPECTRALIS with Flex Module ... recall (Heidelberg Engineering GmbH)
Medical deviceClass IIReported September 30, 2026 · Wheels may come loose when module is being pushed or pulled during movement or transportation, affecting stability of the stand. The stand may tip over as a... - Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5 recall (Boston Scientific Corporation)
Medical deviceClass IReported September 30, 2026 · Tip may fracture or detach, leading to device fragments remaining within the patient or migrating through the vasculature. Patient impact may include prolonged... - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides. - INCA recall (CooperSurgical, Inc.)
Medical deviceClass IReported September 30, 2026 · Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP... - INCA recall (CooperSurgical, Inc.)
Medical deviceClass IReported September 30, 2026 · Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP... - Pi-Cardia Inc. ShortCut REF: Z-A-20.003-US recall (PI CARDIA LTD)
Medical deviceClass IIReported September 23, 2026 · Transfemoral catheter, positing arm may detached due to weld issue. - CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes:... recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under... - Reign Medical Clench Staple System recall (F & A Foundation)
Medical deviceClass IIReported September 23, 2026 · Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established. - Convenience kits CATARACT PACK DYNJ59881A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - SCORPIO + MOBILE BEARING PCS 78-5-0910 SYSTEM ONE BIPOLAR 40MM 6074-4022 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - TRIDENT 0¿ POLY INSERT 28mm ID 620-00-28D Orthopaedic implant components... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - BEARING AND AXLE BUSHING ASSY STD ELBOW C-M113-1-301 KRH REV TIB INS 16mm THK... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - ABG I ACETABULAR INSERT HOODED 28mm ID X 48mm C-M079-2-801 ARC2F ACETABULAR... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 ... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - OMNIFIT SERIES I ACET. INSERT 10¿ 22mm ID Catalog No. 2001-2246 Orthopaedic... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic... recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported September 23, 2026 · Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential... - Captus 4000e Thyroid Uptake System recall (Mirion Technologies (Capintec), Inc.)
Medical deviceClass IIReported September 23, 2026 · Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5... - Et Control recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys CS2 with Et Control recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys CS2 recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Aisys recall (Datex-Ohmeda, Inc.)
Medical deviceClass IIReported September 23, 2026 · Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control... - Boston Scientific Corporation StoneSmart Connect Console Contents: recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 23, 2026 · A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power... - REF:B5ST Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:B5LT Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:B12LT Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:B11LT Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:2B5ST Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - REF:2B5LT Ethicon Endo-Surgery recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported September 23, 2026 · Reusable access port system may crack or seperate during use. - Blood Culture Collection Venipuncture Kit 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIReported September 23, 2026 · Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may... - Kinos Axiom Total Ankle System with Axiom PSR recall (restor3d Inc.)
Medical deviceClass IIReported September 23, 2026 · Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard... - Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT... recall (Wilson-Cook Medical Inc.)
Medical deviceClass IIReported September 23, 2026 · Due to issue with endoscope adherence and inability to spray powder. Firm will provide an updated Instruction for Use (IFU). - Happiest Baby recall (Happiest Baby, Inc)
Medical deviceClass IIReported September 23, 2026 · Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA. - Happiest Baby recall (Happiest Baby, Inc)
Medical deviceClass IIReported September 23, 2026 · Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA. - Brand Name: VERIQA recall (PTW FREIBURG)
Medical deviceClass IIReported September 23, 2026 · When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may... - GM Helix Implant recall (Straumann USA LLC)
Medical deviceClass IIReported September 23, 2026 · There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside. - SunMed Tracheal Tube recall (WELL LEAD MEDICAL CO. LTD)
Medical deviceClass IIReported September 23, 2026 · The 6Fr suction catheter could not pass through the samples smoothly. - Core Services Hub V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Workflow Core Services V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity PACS Server V7 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity PACS V2 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Enterprise Archive V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity Enterprise Archive V2 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - NOxBOXi Nitric Oxide Delivery System. recall (NOXBOX LTD)
Medical deviceClass IIReported September 23, 2026 · Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation. - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Oncology sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Oncology sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Non-Dedicated Gravity Administration Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Plum administration sets recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Haylard UNIV IMAGING BIOPSY TRUCUSTOM recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Haylard BASIC BIOPSY TRAY recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Haylard CONTINUOUS NERVE BLOCK TRAY recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Haylard 18G SINGLE SHOT EPI TRAY recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Impella Optical Controller recall (Abiomed, Inc.)
Medical deviceClass IReported September 23, 2026 · The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. - Impella Optical Controller with the below product descriptions and corresponding... recall (Abiomed, Inc.)
Medical deviceClass IReported September 23, 2026 · The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported September 23, 2026 · The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly. - MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System recall (Bayer Medical Care, Inc.)
Medical deviceClass IIReported September 23, 2026 · Some devices may not have been properly sterilized due to a manufacturing sterilization issue. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Percutaneous Insertion Kit recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported September 23, 2026 · The packaging may not consistently maintain sterile barrier integrity. - Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 23, 2026 · Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically... - Philips PIC iX Essentials REF:867093 recall (Philips North America)
Medical deviceClass IIReported September 23, 2026 · Due to software malfunction, patient information system may freeze and become unresponsive. - Philips Patient Information Center iX REF:866389 recall (Philips North America)
Medical deviceClass IIReported September 23, 2026 · Due to software malfunction, patient information system may freeze and become unresponsive. - Medline Convenience Kit: OPEN HEART A PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be... - StatStrip Glucose and B- Ketone meter. Model No: 66429. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose and B- Ketone meter. Model No: 63910. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose Hospital Meter System. Model No: 66739. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system. recall (Nova Biomedical Corporation)
Medical deviceClass IReported September 23, 2026 · A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a... - Medline Convenience Kits: 1) DYNDB3086D recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) DYNDH1193 recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) DYKM1000B recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) ACC010308A recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the...