Recalls in Wisconsin (page 31)
4031 recalls.
- Azurion 5 M20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 5 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 7 M20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 7 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 7 B20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 7 B12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 3 M15 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Azurion 3 M12 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/15 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/15 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD20/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD10 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD20 Biplane OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD20 OR Table recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD20 Biplane recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD10/10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD10 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - ALLURA Xper FD10F recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Allura Xper FD10C recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. - Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported April 8, 2026 · A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate... - Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿... recall (ReCor Medical Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use. - Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿... recall (ReCor Medical Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use. - Philips Respironics Trilogy Evo Universal recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. - Philips Respironics Trilogy EV300 recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. - Philips Respironics Trilogy Evo O2 recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. - Philips Respironics Trilogy Evo recall (Philips Respironics, Inc.)
Medical deviceClass IReported April 8, 2026 · In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths. - Samson International Recalls Bellevue and Oaklynn Canopy Bed Frames Due to Impact and Injury Hazards
Consumer productReported April 3, 2026 · The canopy beams of the bed frames can collapse primarily when the bed is moved, posing impact and injury hazards to consumers. - Tuymec Minoxidil Hair Growth Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by DrHealBeauty
Consumer productReported April 3, 2026 · The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging is... - Sam's Club Recalls Member's Mark Children's Pajama Sets Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Consumer productReported April 3, 2026 · The recalled pajama sets violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children. - HTRC and Haisito T400 Battery Chargers Recalled Due to Risk of Serious Injury and Death from Fire Hazard; Manufactured by Huizhou Haitan Technology
Consumer productReported April 3, 2026 · The chargers can ignite or cause a connected battery to ignite, posing a fire hazard and risk of serious injury and death. - Sangohe Reannounces and Expands Adult Portable Bed Rails Recall Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
Consumer productReported April 3, 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... - E Mishan Recalls Granitestone Diamond Pro Blue Stainless Sauté Pans Due to Impact and Burn Hazards
Consumer productReported April 3, 2026 · The metal cap on the screw that connects the sauté pan to the handle can become detached and forcefully eject when heated, posing impact and burn hazards to... - TecFlox Hair and Beard Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
Consumer productReported April 3, 2026 · The hair and beard growth serum contains minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottles... - ELENKER Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Fuzhou Shiahaha Cultural Industry Development
Consumer productReported April 3, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - OCUN NA Recalls Condor HMS Triple Carabiners Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported April 3, 2026 · The carabiner's gate can malfunction where the gate does not close automatically and has to be closed manually by hand, posing a risk of serious injury or... - Coluans Christmas Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by BUDI Official
Consumer productReported April 3, 2026 · The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell... - Gavoyeat Halloween Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by CSZWEICD
Consumer productReported April 3, 2026 · The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell... - Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Ball Ban; Sold on Amazon by Beestech
Consumer productReported April 3, 2026 · The recalled spiral tower toy sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of... - SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD recall (Savannah Bee Company Inc.)
FoodClass IIReported April 1, 2026 · Undeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard", but the... - Pepsin 1:3000 Powder recall (American Laboratories, LLC)
FoodClass IIReported April 1, 2026 · Potential Salmonella contamination. - Pepsin 1:10 recall (American Laboratories, LLC)
FoodClass IIReported April 1, 2026 · Potential Salmonella contamination. - Pepsin Full Strength Powder recall (American Laboratories, LLC)
FoodClass IIReported April 1, 2026 · Potential Salmonella contamination. - Item 6430153 Ajinomoto Vegetable Gyoza Dumplings. Net wt. 24.7oz. per bag. Retail box recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package.... recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12ct. Retail bag recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 81153 Kroger Chinese Inspiration Vegetable Fried Rice - Blend of long grain rice... recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A... recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 5654390 Ajinomoto Golden Tiger Vegetable Fried Rice - Long grain white rice and... recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made with hijiki seaweed recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 5650883 Ajinomoto Teppanyaki Style Vegetable Fried Rice - Japanese-style fried... recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 5650233 Trader Joe's Vegetable Fried Rice recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame recall (Ajinomoto Foods North America Inc.)
FoodClass IIReported April 1, 2026 · Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide. - BD Alaris" System with Guardrails" Suite MX with Point of Care Unit recall (CareFusion 303, Inc.)
Medical deviceClass IIReported April 1, 2026 · Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi... - MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61 recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported April 1, 2026 · Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61... - 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... - 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). - BioFlo DuraMax Catheter recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - DuraMax Chronic Hemodialysis Catheter recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - 16F Dual Valved Splittable Sheath Introducer recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - ProGuide Chronic Dialysis Catheters recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - CentrosFLO Hemodialysis Catheters recall (Merit Medical Systems, Inc.)
Medical deviceClass IReported April 1, 2026 · 16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure... - Nuts.com recall (Nuts.com Inc.)
FoodClass IReported April 1, 2026 · Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy. - Chilli Spanish Peanuts recall (Western Mixers Produce & Nuts, Inc.)
FoodClass IIReported April 1, 2026 · Foreign object (glass) found inside sealed container of finished product. - Chilli Spanish Peanuts recall (Western Mixers Produce & Nuts, Inc.)
FoodClass IIReported April 1, 2026 · Foreign object (glass) found inside sealed container of finished product. - Meclizine Hydrochloride Tablets recall (Amerisource Health Services LLC)
DrugClass IIReported April 1, 2026 · Failed tablet specifications. - Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 1, 2026 · Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract... - Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 1, 2026 · Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract... - Octreotide Acetate for Injectable Suspension recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 1, 2026 · Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract... - Levothyroxine Sodium Tablets USP 150 mcg recall (MACLEODS PHARMA USA, INC)
DrugClass IIReported April 1, 2026 · Subpotent Drug - CUROSURF recall (Chiesi USA, Inc.)
DrugClass IIReported April 1, 2026 · Lack of Assurance of Sterility - Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit recall (Radnostix)
DrugClass IIIReported April 1, 2026 · Failed Tablet/Capsule Specifications - Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING recall (Medline Industries, LP)
Medical deviceClass IIReported April 1, 2026 · Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound... - 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 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... - 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 /... - 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. - Brand Name: I.T.S. Pelvic Reconstruction System recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - HLS - Hand Locking Plates System with the below descriptions and corresponding article... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - HCS - Headless Compression Screw System recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - FLS - Foot Locking Plates System and HOL - Hallux Osteotomy Locking Plate with the... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - I.T.S. DUL recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for...