Check a product
Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk during spine surgery
Surgify Medical's Halo 5.4 mm burr, used in minimally invasive spinal surgery, may break during use. The company has identified this risk and is notifying healthcare facilities.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk
Surgify Medical's Halo 5.4 mm burr (model 54.125.NVG.U1) may break during bi-portal endoscopic spinal surgery. The company has identified this risk and is working to update instructions for use. No injuries have been reported.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk
Surgify Medical's Halo 5.4 mm burr (Model 54.125.NVG.H1) may break during bi-portal endoscopic spinal surgery. The device has been distributed across multiple U.S. states. No injuries have been reported.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk in spine surgery
Surgify Medical's Halo 5.4 mm burr, used in minimally invasive spinal surgery, may break during the procedure. The company has identified this risk and is recalling affected units.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo surgical burr recalled for breakage risk
Surgify Medical's Halo 5.4 mm surgical burr (Model 54.085.SHD.H1) may break during bi-portal endoscopic spinal surgery. The risk affects all product lots distributed in the US until updated instructions are implemented.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk in spinal surgery
Surgify Medical's Halo 5.4 mm burr (Model 54.070.NVG.U1) may break during bi-portal endoscopic spinal surgery (BESS). The risk affects all lots distributed in the U.S. until updated instructions are provided.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk in spinal surgery
Surgify Medical's Halo 5.4 mm burr, used in minimally invasive spinal surgery, may break during the procedure. This affects spinal surgery burrs distributed across the US.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk in spinal surgery
Surgify Medical's Halo 5.4 mm extendable burr (Model 54.000.SEE.U1) may break during bi-portal endoscopic spinal surgery (BESS). The defect affects 8 units distributed across the US. No injuries have been reported.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk
Surgify Medical's Halo 5.4 mm extendable burr may break during bi-portal endoscopic spinal surgery (BESS). This surgical instrument is used by spine surgeons, and burr breakage during the procedure could complicate the operation. No injuries have been reported.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo spinal burr recalled for breakage risk
Surgify Medical's Halo 40 mm burr tool, used in minimally invasive spinal surgery, may break during the procedure. This could interrupt surgery or leave fragments in the surgical site. The recall affects all units until the manufacturer updates instructions for use.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk in spinal surgery
Surgify Medical's Halo 4.0 mm burr (Model 40.125.NVG.H1) may break during bi-portal endoscopic spinal surgery (BESS). The breakage could occur while the burr is in use, potentially affecting the procedure.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo surgical burr recalled for breakage risk
Surgify Medical's Halo 4.0 mm burr, used in spinal surgery, may break during the procedure. The affected model is 40.070.NVG.U1. This issue affects all lots currently distributed until the manufacturer updates its instructions.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo surgical burr recalled for breakage risk
Surgify Medical's Halo 4.0 mm short burr (model 40.070.NVG.H1) may break during bi-portal endoscopic spinal surgery (BESS). The breakage could occur during the procedure and compromise the surgical outcome. This affects all lots distributed in the US until updated instructions are implemented.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo spinal burr recalled for breakage risk
Surgify Medical's Halo 4.0 mm extendable burr, used in spinal surgery, may break during the procedure. The breakage could occur during bi-portal endoscopic spinal surgery (BESS). This affects all lots until the manufacturer updates the product instructions.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk in spinal surgery
Surgify Medical's Halo 4.0 mm extendable burr (Model 40.000.SEE.H1) may break during bi-portal endoscopic spinal surgery (BESS). The breakage could occur during the procedure and potentially complicate the surgery. This affects 112 units distributed across several US states.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk
Surgify Medical's Halo 3.0 mm burr (Model 30.125.NVG.U2) may break during bi-portal endoscopic spinal surgery (BESS). The issue affects all lots until updated instructions are implemented. No injuries have been reported.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk
Surgify Medical's Halo 3.0 mm burr (Model 30.070.NVG.U2) may break during bi-portal endoscopic spinal surgery (BESS). The risk affects all lots distributed in the US until updated instructions are provided.
- 2026-07-01FDA-DeviceSURGIFY MEDICAL OYClass IISurgify Halo burr recalled for breakage risk during spinal surgery
Surgify Medical's Halo 3.0 mm extendable burr (Model 30.000.SEE.U2) may break during bi-portal endoscopic spinal surgery. The breakage could occur during the procedure. This affects 15 units distributed across several US states.
- 2026-07-01FDA-DeviceIPG Medical CorporationClass IIIPG Medical Thuvera Laser Console recalled for false error display
A software issue in the Thuvera Laser Console (Software Version 2.2) causes the device to display a false error code 5018. This anomaly may lead clinicians to misinterpret the device status during operation.
- 2026-07-01FDA-DeviceGE Medical Systems SCSClass IIGE Healthcare AW Server 3.2 recalled for wrong patient images risk
GE Healthcare's AW Server 3.2 ext.6.5 has a software issue that can cause the system to display a previous patient's medical images instead of the correct patient's images when launching certain applications. There is no warning or error message when this happens. If a radiologist or clinician does not notice the error, they could misread images, make wrong diagnoses, or recommend incorrect treatment.
- 2026-07-01FDA-DeviceStryker NeurovascularClass IIStryker INZONE coil detachment device recalled for battery failure
Stryker Neurovascular's INZONE Detachment System devices may experience premature battery drain, causing them to fail to power on, display faint indicators, or be unable to detach an embolization coil as intended. If a device fails during a procedure, medical staff may need to use an alternative technique to complete the intervention.
- 2026-07-01FDA-DeviceAcumed LLCClass IIAcumed Hexalob Screws recalled for breakage risk
Acumed Hexalob Screws used in wrist fixation systems may break during use due to a manufacturing error. The affected screws come in various sizes (2.7mm and 3.0mm) and have been distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DeviceZimmer, Inc.Class IIZimmer reamer guide recalled for breakage during use
Zimmer identified a defect in the Off-Axis Alliance Glenoid Reamer Guide where plastic components can catch and break during the reaming procedure. Five complaints of this issue have been reported. The affected surgical instrument was distributed nationwide, with 13 units involved.
- 2026-07-01FDA-DeviceZimmer, Inc.Class IIZimmer shoulder implant guide recalled for breakage risk
Zimmer, Inc. is recalling a surgical guide used during shoulder implant procedures. Five reports have identified that the plastic guide can catch and break during the reaming step of surgery, potentially affecting the procedure.
- 2026-07-01FDA-DeviceZimmer, Inc.Class IIZimmer shoulder reamer guide recalled for breakage risk
The plastic guide in Zimmer's Off-Axis Comprehensive Shoulder System reamer tool can catch during the reaming procedure, causing it to break. The FDA received five complaints about this issue. No injuries have been reported.
- 2026-07-01FDA-DeviceZimmer, Inc.Class IIZimmer shoulder reamer guide recalled for breakage risk
Zimmer has recalled a plastic reamer guide used during shoulder surgery due to reports of the guide catching and breaking during the reaming procedure. Five complaints have been received. No injuries have been reported.
- 2026-07-01FDA-DeviceZimmer, Inc.Class IIZimmer shoulder reamer guide recalled for breakage risk
Zimmer has recalled a plastic reamer guide used in shoulder surgery because the plastic can catch and break during the reaming procedure. Five complaints have been received describing this issue. No injuries have been reported.
- 2026-07-01FDA-DevicePFM MEDICAL INC.Class IIPFM Medical snare catheters recalled for tissue irritation risk
PFM Medical's Multi-Snare Set catheters (5 mm and 10 mm models) failed to meet biocompatibility safety standards. If used, the device material could cause localized inflammation and tissue irritation when in contact with blood vessels.
- 2026-07-01FDA-DeviceVentec Life Systems, Inc.Class IIVentec VOCSN+Pro ventilator recalled for backup alarm failure
Ventec Life Systems' VOCSN+Pro respiratory ventilator may have a damaged backup battery that powers the alarm system. If primary power is lost and the backup battery is depleted or absent, the backup alarm may not sound to alert caregivers of the power loss.
- 2026-07-01FDA-DeviceTMJ Solutions IncClass IITMJ Solutions bilateral implant recalled for component mismatch
TMJ Solutions Inc. has recalled one custom temporomandibular joint implant (model CHG020) that may contain incorrect patient-specific components. The mismatch caused a poor fit, resulting in a right-sided open bite for the affected patient.