Recalls in Kansas (page 32)
4012 recalls.
- Brand Name: Olympus PKS Cutting Forceps w/Cord recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus HALO PKS Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus PK Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: Olympus Everest Bipolar Cutting Forceps recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can... - Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name:... recall (AMO Puerto Rico Manufacturing, Inc.)
Medical deviceClass IIReported April 1, 2026 · Due to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as... - Custom Abutment AS Ti recall (Straumann USA LLC)
Medical deviceClass IIReported April 1, 2026 · A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 /... - Custom Abutment Ti recall (Straumann USA LLC)
Medical deviceClass IIReported April 1, 2026 · A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 /... - Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler recall (Koven Technology, Inc.)
Medical deviceClass IIReported April 1, 2026 · Product labeling includes a fetal indication for use that is not cleared under its 510(k). - Drill Plate recall (Orthalign, Inc)
Medical deviceClass IIReported April 1, 2026 · Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) - Drill Plate recall (Orthalign, Inc)
Medical deviceClass IIReported April 1, 2026 · Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm) - Philips Respironics Trilogy Evo Universal recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 1, 2026 · Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by... - Philips Respironics Trilogy EV300 recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 1, 2026 · Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by... - Philips Respironics Trilogy Evo O2 recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 1, 2026 · Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by... - Philips Respironics Trilogy Evo recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 1, 2026 · Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by... - Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 1, 2026 · The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. - Imactis CT-Navigation System recall (GE Medical Systems, LLC)
Medical deviceClass IIReported April 1, 2026 · There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position. - Handy Solutions Neck & Shoulders Heating Pad recall (Navajo Manufacturing Company)
Medical deviceClass IReported April 1, 2026 · If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad... - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - Flexible Cryoprobe recall (Erbe USA Inc)
Medical deviceClass IReported April 1, 2026 · Probes may rupture/burst during activation - MPINOI 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; Sold on Amazon by Bioenrrty
Consumer productReported March 27, 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... - DIY Cold Plunge Recalls Sauna Heater Kits Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported March 27, 2026 · Electrical conductors within the sauna heater kits can overheat, posing a fire hazard and risk of serious injury or death. - FUNTOK Ride-On Trucks Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by Shenzhen Luobei Trading
Consumer productReported March 27, 2026 · The truck's circuit board can overheat and ignite, posing fire and burn hazards. - Petzl America Recalls Nomic and Ergonomic Ice Climbing Axes Due to Fall Hazard; Risk of Serious Injury or Death
Consumer productReported March 27, 2026 · The ice axe shaft can break at the handle during use, posing a fall hazard, which can result in serious injury or death. - CCCEI Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Fire; Sold by Middle Way Electronics
Consumer productReported March 27, 2026 · The power strips do not contain supplementary overcurrent protection, which creates a risk of fire if the power strips are overloaded. The resulting fire can... - GLMZZ Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
Consumer productReported March 27, 2026 · The magnet ball toys violate the mandatory standard for toys because they are high-powered magnets, posing an ingestion hazard to children. When high-powered... - Sunnyyes LED Mini Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
Consumer productReported March 27, 2026 · The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because the lights contain lithium coin... - DuraTrac Recalls Stainless Steel Gas Connectors Due to Fire Hazard
Consumer productReported March 27, 2026 · The recalled DuraTrac gas connectors contain a manufacturing defect that could cause a gas leak, posing a fire hazard to consumers. - AirClub Convertible Bassinets Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Bedside Sleepers
Consumer productReported March 27, 2026 · The recalled convertible bassinets violate the mandatory standard for bedside sleepers because the mechanism used to attach the product to the adult bed... - Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Two Deaths Reported
Consumer productReported March 27, 2026 · When the recalled bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress. This... - 4our Kiddies Tip Restraint Kits Recalled Due to Tip-Over Hazard; Risk of Serious Injury and Death
Consumer productReported March 27, 2026 · The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards that can result in... - Nexgrill Recalls Over 10.2 Million Metal Wire Bristle Grill Brushes Due to Ingestion Hazard; Sold at Home Depot
Consumer productReported March 27, 2026 · Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that... - Brand Name: Welch Allyn recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported March 25, 2026 · Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible... - Webcol Alcohol Prep pad recall (Cardinal Health 200, LLC)
DrugClass IReported March 25, 2026 · Non-Sterility: microbial contamination identified as Paenibacillus phoenicis - Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%* recall (Apotex Corp.)
DrugClass IIReported March 25, 2026 · Lack of Assurance of Sterility - Dexamethasone Sodium Phosphate Injection recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIReported March 25, 2026 · Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs... - Children's Ibuprofen Oral Suspension recall (STRIDES PHARMA INC)
DrugClass IIReported March 25, 2026 · Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product. - Battery Charging Station recall (Datascope Corp.)
Medical deviceClass IIIReported March 25, 2026 · The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to ... - Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number:... recall (Hologic, Inc.)
Medical deviceClass IIReported March 25, 2026 · Due to product exhibiting potential to generate either invalid or false negative results. - Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number:... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported March 25, 2026 · After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Convatec recall (ConvaTec, Inc)
Medical deviceClass IIReported March 25, 2026 · Drainable large pouch may leak due to manufacturing issue. - Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion ... recall (Elekta, Inc.)
Medical deviceClass IIReported March 25, 2026 · Due to adapter not being properly aligned or locked in place. - Cub Pediatric Crib recall (Stryker Medical Division of Stryker Corporation)
Medical deviceClass IIReported March 25, 2026 · Cribs sold in the USA are missing two access door warning labels. - Artegraft Vascular Graft recall (LeMaitre Vascular, Inc.)
Medical deviceClass IIReported March 25, 2026 · Labeling mix-up resulting in the incorrect lot outer packaging of product. - MICS3 Angled Sagittal Saw Attachment recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported March 25, 2026 · A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the... - Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported March 25, 2026 · There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local... - Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported March 25, 2026 · There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local... - Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported March 25, 2026 · There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local... - Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software... recall (Abbott Diagnostics Scarborough, Inc.)
Medical deviceClass IIReported March 25, 2026 · It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use. - Aisstxoer Adult Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by YXTDZ Store
Consumer productReported March 19, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional... - Amazon Recalls Amazon Basics Camping Folding Pocket Knives Due to Laceration Hazard
Consumer productReported March 19, 2026 · The folding mechanism on the blade can fail to remain properly secured in the closed position, posing a laceration hazard. - Electrolux Group Recalls Frigidaire Gas Ranges Due to Burn Hazard
Consumer productReported March 19, 2026 · The ovens in the ranges can experience a delayed ignition of the oven's bake burner, posing a risk of burn hazards to users. - Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by Goregent Official Store
Consumer productReported March 19, 2026 · The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a... - Lifetime Brands Recalls BUILT LUUM Light Up Tumblers Due to Risk of Choking and Battery Ingestion Hazards
Consumer productReported March 19, 2026 · The recalled LED tumblers can break, making the button cell batteries accessible to children and posing choking and ingestion hazards. When button cell or coin... - Specialized Bicycle Components Recalls Specialized Turbo Como SL Electric Bicycles Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported March 19, 2026 · The bike's fork steerer tube can develop a small fatigue crack that can lead to a progressive failure of the fork, posing a fall hazard. - Tainoki Fine Furniture Recalls Office Chairs Due to Risk of Serious Injury and Fall Hazard
Consumer productReported March 19, 2026 · The recalled chairs' base can bend, posing a fall hazard. - Wagner Spray Tech Recalls 900 Series Power Steamers Due to Burn Hazard
Consumer productReported March 19, 2026 · The attached hose can get excessively hot and the nozzle/gun can expel hot water during use and after the trigger is engaged, posing a serious burn hazard to... - VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz recall (Palmetto Gourmet Foods Inc.)
FoodClass IIReported March 18, 2026 · Product contains undeclared Yellow #5 - VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz recall (Palmetto Gourmet Foods Inc.)
FoodClass IIReported March 18, 2026 · Product contains undeclared Yellow #5 - Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor recall (International Life Sciences)
Medical deviceClass IIReported March 18, 2026 · Augmentation devices failed bacterial endotoxin testing. - Artelon FlexBand Plus Ref: 41054 & 41057 recall (International Life Sciences)
Medical deviceClass IIReported March 18, 2026 · Augmentation devices failed bacterial endotoxin testing. - Artelon FlexBand Dynamic Matrix Ref: 31057 recall (International Life Sciences)
Medical deviceClass IIReported March 18, 2026 · Augmentation devices failed bacterial endotoxin testing. - CHEMISTRY ANALYZER AU5800 recall (Beckman Coulter Mishima K.K.)
Medical deviceClass IIReported March 18, 2026 · A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15... - DxC 700 AU recall (Beckman Coulter Mishima K.K.)
Medical deviceClass IIReported March 18, 2026 · A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15... - PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers:... recall (Physio-Control, Inc.)
Medical deviceClass IIReported March 18, 2026 · Due to pediatric defibrillator electrode delamination - Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog... recall (Exactech, Inc.)
Medical deviceClass IIReported March 18, 2026 · Impactor handle may be missing cross-pin - Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog... recall (Exactech, Inc.)
Medical deviceClass IIReported March 18, 2026 · Impactor handle may be missing cross-pin - Rosabella brand MORINGA recall (Ambrosia Brands LLC)
FoodClass IReported March 18, 2026 · Product may be contaminated with Salmonella - Icosapent Ethyl Capsules recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported March 18, 2026 · Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient. - Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE recall (Medline Industries, LP)
Medical deviceClass IIReported March 18, 2026 · Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may... - Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN recall (Medline Industries, LP)
Medical deviceClass IIReported March 18, 2026 · Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may... - Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported March 18, 2026 · The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target... - Brand Name: Bisaf Strep A Self-Test. Test for detection of group A streptococcal... recall (Altruan GmbH)
Medical deviceClass IIReported March 18, 2026 · Product not cleared by the FDA. - Clearest Strep-A Cassette Test. Test to determine the presence of group A streptococci recall (Altruan GmbH)
Medical deviceClass IIReported March 18, 2026 · Product not cleared by the FDA. - Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic... recall (Altruan GmbH)
Medical deviceClass IIReported March 18, 2026 · Product not cleared by the FDA. - CLARITY II Laser System recall (Lutronic Corporation)
Medical deviceClass IIReported March 18, 2026 · Reports of devices sparking/popping and potentially burning patients. - HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product... recall (Covidien LLC)
Medical deviceClass IIReported March 18, 2026 · Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote... - EndoVive Safety PEG Kit recall (Boston Scientific Corporation)
Medical deviceClass IIReported March 18, 2026 · Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result in loss of... - Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm recall (Medartis AG)
Medical deviceClass IIReported March 18, 2026 · Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws. - Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm recall (Medartis AG)
Medical deviceClass IIReported March 18, 2026 · Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws. - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution...