Recalls in Colorado (page 30)
3947 recalls.
- Brand Name: da Vinci S recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported April 8, 2026 · Due to increased complaints for broken/frayed grip cables for reusable instruments. - Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the... - Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 8, 2026 · Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the... - Sterile Radiology Procedure Kits recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility. - Vue Motion V12. Product Number: 1017979. recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported April 8, 2026 · Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence. - Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT ... recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage.... - ENFIT G-TUBE CONNECTOR recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage.... - Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 recall (Stryker Communications)
Medical deviceClass IIReported April 8, 2026 · Surgical light assembly may not adequate support the weight of the ceiling cover. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - Artoura Breast Tissue Expanders Reference Numbers:... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH ... recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113 recall (Mentor Texas, LP.)
Medical deviceClass IIReported April 8, 2026 · Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break. - 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... - 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... - 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... - 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). - 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... - I.T.S. LRS 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... - Distal Humeral Plates with Angular Stability with the below descriptions and... 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. Fibula Plate PROlock with Angular Stability with the below descriptions and... 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... - 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... - I.T.S. Screw System with the below descriptions and corresponding article numbers. ... 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. Straight Plate with Angular Stability with the below descriptions and... 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... - Olecranonplate with Angular Stability with the below descriptions and corresponding... 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... - Pilonplate with Angular Stability 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... - FR.O.H. Calcaneus Repair System with the following description: Anterolateral... 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... - Brand Name: Humeral Head Plate with Angular Stability 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... - Claviculaplate with Angular Stability 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... - Volar Radius Plate with Angular Stability with the following description: Radius Plate... 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... - 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...