Recalls in Iowa (page 30)
3929 recalls.
- Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - Burlington Medical recall (Burlington Medical, LLC)
Medical deviceClass IIReported April 8, 2026 · Potential for attenuation degradation over time, decreasing the lifespan. - MEDLINE ANTERIOR HIP PACK DYNJ64672B recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline kits containing Olympus biopsy valves: 1. BAL KIT recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - THORACIC ROBOTS recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - Airway Exam Kit recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of... - 2.4 VOLT recall (Synthes (USA) Products LLC)
Medical deviceClass IIReported April 8, 2026 · A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an... - 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US. recall (Synthes (USA) Products LLC)
Medical deviceClass IIReported April 8, 2026 · A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an... - 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... - 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... - 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 /... - 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... - 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). - 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...