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Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IIMedline Foley catheter kits recalled for surface contamination
Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled because the catheters have an increased amount of raw material on their surface. This material may cause staining and could potentially be harmful if the catheters are used.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IIMedline Foley catheter kits recalled for surface contamination
Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled. The catheters contain increased amounts of raw material on the surface, which may cause staining and could be harmful if the catheters are used.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IIMedline Foley catheter kits recalled for surface contamination
Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) include catheters with excess raw material on the surface. This material may cause staining and could be harmful if the catheters are used.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IIMedline Bard Foley Catheter kits recalled for surface contamination
Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled due to increased raw material on the catheter surface. This contamination may cause staining and could potentially be harmful if the catheters are used.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IIMedline Foley catheter kits recalled for surface contamination
Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French) have been recalled because the catheters have an increased amount of raw material on their surface. This contamination may cause staining and could be harmful to patients.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IIMedline urology kits recalled for defective Foley Catheters
Medline convenience kits used in urology robotic procedures contain Bard Silastic Foley Catheters with excess raw material on the catheter surface. This material may cause staining and could potentially harm patients. The catheters were originally recalled by the manufacturer due to this manufacturing defect.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IIMedline DaVinci Prostate Pack recalled for defective catheters
Medline convenience kits containing Bard Silastic Foley Catheters have been recalled because the catheters have an increased amount of raw material on their surface. This material may cause staining and could be harmful if the catheters are used.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IIMedline Foley catheter kits recalled for surface contamination risk
Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled because the catheters have an increased amount of raw material on their surface. This contamination may cause staining and could be harmful if the catheters are used.
- 2026-07-29FDA-DeviceMedtronic MiniMed, Inc.Class IIMedtronic MiniMed Go App recalled for missed nighttime alerts
Medtronic MiniMed Go app versions 1.0.0 and 1.1.0 have a software bug: when the "Set day and night" feature is turned off, missed-dose and high-glucose alerts may fail to trigger at night. This means users may not realize they've missed insulin doses, potentially delaying treatment and raising blood sugar levels dangerously.
- 2026-07-29FDA-DeviceEmano Metrics, Inc.Class IIEmano Flow app recalled for inaccurate urinary flow measurements
Emano Flow, a smartphone app that measures urinary flow rate and volume, produced inaccurate results during a two-month period (March 22–May 29, 2026). The app recorded audio at an incorrect frequency setting, causing measurements to be systematically over-reported. The company has provided corrected results to healthcare teams.
- 2026-07-29FDA-DeviceOlympus Corporation of the AmericasClass IIOlympus UHI-4 insufflation unit recalled for display and air delivery failure
The Olympus UHI-4 insufflation unit may experience unexpected shutdowns where the front panel display turns off and air delivery stops during use. This affects about 3,087 units distributed worldwide. No injuries have been reported.
- 2026-07-29FDA-DeviceKENT IMAGING, INC.Class IIKent Imaging SnapshotGLO wound imager recalled for battery charge issue
The SnapshotGLO device's software cannot recognize when its battery has fully discharged into a low-power shipping mode. When this happens, the device will not resume charging when plugged in and becomes temporarily unusable until the issue is corrected.
- 2026-07-29FDA-DeviceMicro Therapeutics, Inc.Class IIMicro Therapeutics embolization devices recalled for incorrect labeling
Micro Therapeutics Pipeline Flex Embolization Devices have incorrect labeling on some units. Devices labeled as 3.0 mm x 20 mm actually contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm actually contain 20 mm implants. This mismatch could lead to incorrect implant selection during surgery.
- 2026-07-29FDA-DeviceAVID Medical, Inc.Class IIHalyard line insertion pack recalled for seal defect risk
Certain Halyard STANDARD LINE INSERTION PACK kits (Model PVHM234-01) have a defect in the silicone seal that may not seal properly. This defect can cause the seal to dome inward, potentially blocking fluid flow or allowing fluid to leak where it shouldn't.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific TheraSphere 360 Y-90 dose calculation software issue
The TheraSphere 360 Y-90 Management Platform has a software bug that can cause incorrect dose calculations. When a user modifies calculation inputs and recalculates, the new dose is computed correctly on screen, but vials previously added to the cart do not automatically update to match the revised calculation.
- 2026-07-29FDA-DevicePenumbra, Inc.Class IIPenumbra RED 68 catheter recalled for fracture risk
Penumbra System RED 68 Reperfusion Catheters (REF: RED68KIT) may fracture during use due to a manufacturing defect. The affected lots are H00008699, H00008701, H00008702, H00008703, and C00020038. These catheters were distributed worldwide, including throughout the United States.
- 2026-07-29FDA-DevicePrismatik Dentalcraft, Inc.Class IISilent Nite sleep appliance recalled for missing FDA clearance
Prismatik Dentalcraft distributed Silent Nite Sleep Appliances (a mandibular advancement device for snoring and sleep apnea) without obtaining required FDA clearance. The devices were sold in multiple states before the clearance status was identified.
- 2026-07-29FDA-DeviceMedtronic NeurosurgeryClass IIMedtronic Ventriculostomy Kit recalled for endotoxin contamination
Medtronic Neurosurgery's Ventriculostomy Kit (REF: 46154) may contain endotoxin levels higher than safe limits for devices that contact cerebrospinal fluid during brain surgery. Endotoxin exposure can trigger acute inflammation in the brain and nervous system.
- 2026-07-29FDA-DevicePIE Medical Imaging B.V.Class IIPIE Medical 3mensio software recalled for cardiac measurement errors
The 3mensio Workstation software may report heart and vessel measurements that are 0.8% to 34% larger than the actual size when specific conditions are met: the software is used with access only to 3D Echo or Mitral 3D Echo features, and the analysis involves Philips 3D echo datasets that contain Color Doppler data. This could lead to incorrect clinical measurements used in patient care decisions.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IMedline procedure kits recalled for medication quality issues
Medline medical procedure kits used for knee and hip surgeries contain pain management medications with quality issues that could make them less effective. The affected kits were distributed to hospitals and surgical centers in Missouri, Colorado, and Illinois.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IMedline HIP CDS-LF procedure kit recalled for drug ineffectiveness
Medline medical procedure convenience kits (model HIP CDS-LF) contain pain management medications with quality issues that could make the medication ineffective. The affected kits were distributed in Missouri, Colorado, and Illinois. No injuries have been reported.
- 2026-07-29FDA-DeviceAVID Medical, Inc.Class IIHalyard EYE PACK recalled for incorrect Betadine concentration
Certain Halyard EYE PACK convenience kits (Model LVEY27) contain Betadine solution at an incorrect concentration. The kits were distributed nationwide, primarily in California. No injuries have been reported.
- 2026-07-29FDA-DeviceSEASPINE ORTHOPEDICS CORPORATIONClass IISeaSpine Polyaxial Head recalled for potential intraoperative pop-off
SeaSpine Orthopedics has recalled certain Polyaxial Head spinal implants (REF 41-3010) due to a manufacturing error that may cause the polyaxial head to detach from the screw during surgery after insertion. This could require additional surgical intervention. The recall affects 796 units distributed worldwide, including nationwide US distribution and locations in Chile and Australia.
- 2026-07-29FDA-DeviceOlympus Corporation of the AmericasClass IIOlympus 4K UHD LCD Monitor recalled for connector faults
Olympus has identified a potential fault in the HDMI and DisplayPort connectors on certain OEV321UH 4K UHD LCD Monitors. This fault can result in image loss or display abnormalities. The recall affects 10 units with specific serial numbers distributed in Ohio, California, New Jersey, Florida, and Japan.
- 2026-07-29FDA-DeviceFerno-Washington IncClass IIFerno-Washington Power F2 stretcher system recalled for jamming risk
The roller assembly on the Ferno-Washington Power F2 Powered Fastening System may wear unevenly and deform, causing the rail mechanism to jam. If this happens, the stretcher cannot move along the rail—either with the powered system or manually—potentially delaying patient transport to a hospital.
- 2026-07-29FDA-DeviceICU Medical Inc.Class IIICU Medical Hotline Fluid Warming Set recalled for leakage risk
ICU Medical's Hotline Fluid Warming Set (model L-70), a single-use device used to warm blood and IV fluids before delivery to patients, may leak due to inadequate solvent application at the tubing-to-connector bond in certain production lots. This defect could affect proper fluid delivery during patient care.
- 2026-07-29FDA-DeviceParagon 28, Inc.Class IIParagon 28 guide rod recalled for sterile packaging breach
Paragon 28 received two complaints about breaches in the sterile barrier packaging of specific lots of the Phantom Hindfoot TTC/TC Ball Tipped Guide Rod (0.30 mm, 800 mm). The packaging breach could potentially allow contamination of the surgical device before use. No injuries have been reported.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARADRIVE Steerable Sheath recalled for air embolism risk
Boston Scientific identified that certain FARADRIVE Steerable Sheath devices may develop damage to the hemostatic valve if the dilator is not inserted correctly during preparation. Valve damage can allow air to enter the device, which may lead to air embolism—a serious condition where air bubbles reach the bloodstream and heart.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARADRIVE Steerable Sheath recalled for air embolism risk
Boston Scientific identified that certain lots of the FARADRIVE Steerable Sheath (CLEAR) may have a hemostatic valve that can be damaged during device preparation if the dilator is not inserted correctly. Valve damage can allow air to enter, potentially causing an air embolism and patient harm.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARADRIVE sheath recalled for air embolism risk
Boston Scientific has identified that certain lots of the FARADRIVE steerable sheath may develop damage to the hemostatic valve during preparation if the dilator is not inserted correctly. This valve damage can allow air to enter the device, which may lead to air embolism (air in the bloodstream) and patient harm.