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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.
- 2026-07-01FDA-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.
- 2026-07-01FDA-DevicePhilips North America LlcClass IIPhilips Avalon Fetal Monitor recalled for speaker connector defect
Certain Philips Avalon FM 30 fetal monitors have an incorrect speaker connector assembly that can allow device cables to be pulled out of the housing. This defect may cause the speaker to stop working intermittently or permanently, which could affect audio output during monitoring.
- 2026-07-01FDA-DevicePhilips North America LlcClass IIPhilips Avalon FM20 Fetal Monitor recalled for speaker connector defect
Certain Philips Avalon FM20 Fetal Monitors have a speaker connector that was assembled incorrectly. This defect can cause cables to pull out of the device housing, which may result in loss of speaker output—either intermittently or permanently. This affects audio alerts that are critical to clinical monitoring.
- 2026-07-01FDA-DeviceIntuitive Surgical, Inc.Class IIIntuitive Surgical Da Vinci recalled for E-brake failure risk
Certain Da Vinci surgical systems were distributed with a defective E-brake retainer pin. If the structural column fails, this pin can prevent the E-brake from engaging, potentially causing uncontrolled motion of the robotic arm. The pin may also loosen or back out, restricting arm movement or causing uncontrolled motion that could injure patient tissue.
- 2026-07-01FDA-DeviceMedline Industries, LPClass IMedline Convenience Kits recalled for anesthetic quality issues
Medline Convenience Kits containing anesthetic medications (Lidocaine and Bupivacaine injections) were recalled due to quality issues found during an FDA inspection of the supplier. The affected kits are used in medical procedures including central line placement and open heart surgery.
- 2026-07-01FDA-DeviceMedline Industries, LPClass IMedline Convenience Kits recalled for anesthetic quality issues
Medline Convenience Kits containing Arrow Kits and Sets with Lidocaine and Bupivacaine anesthetic injections were recalled due to quality issues found during an FDA inspection of the supplier. The kits are used for central and arterial line procedures in medical settings. A total of 233 units were distributed nationwide.
- 2026-07-01FDA-DeviceMedline Industries, LPClass IMedline open heart kits recalled for anesthetic quality issues
Medline Convenience Kits used in cardiac surgery contain anesthetic medications (Lidocaine and Bupivacaine) that were recalled by their supplier due to quality concerns found during an FDA inspection. About 6,775 affected kits have been distributed to hospitals and surgical centers.
- 2026-07-01FDA-DeviceMedline Industries, LPClass IMedline Convenience Kits recalled for anesthesia injection quality issues
Medline Convenience Kits used in cardiovascular anesthesia room setups contain anesthesia injectables (Lidocaine and Bupivacaine) that were recalled due to quality problems found during an FDA inspection of the supplier. The affected kits are used in hospital operating rooms.
- 2026-07-01FDA-FoodBoichik Bagels, Inc.Class IIBoichik Bagels recalled for undeclared sesame allergen
Boichik Bagels Pumpernickel Mix Bagels may contain sesame seeds that are not declared on the label. People with sesame allergies could have a serious reaction if they eat these bagels. The affected products have best-by dates between May 25, 2026 and August 23, 2026.
- 2026-07-01FDA-FoodBoichik Bagels, Inc.Class IIBoichik Bagels Tuna Salad recalled for undeclared egg
Boichik Bagels Tuna Salad contains eggs in the mayonnaise ingredient, but the product label does not list eggs in the allergen "Contains" statement. People with egg allergies could have a serious reaction if they consume this product.
- 2026-07-01FDA-FoodBoichik Bagels, Inc.Class IIBoichik Bagels Whitefish Salad recalled for undeclared egg
Boichik Bagels Whitefish Salad contains eggs in the mayonnaise ingredient, but the product label does not list eggs in the allergen "Contains" statement. People with egg allergies who rely on the label could have a serious reaction if they eat this product.
- 2026-07-01FDA-FoodCERELES EN GENERAL SASClass IPearl Milling Company Original Pancake & Waffle Mix Complete (Mezcla Para Panqueques y Waffles) Net Wt 5.99 oz (170 g). Packed in 50 - 5.99 oz BOPP Pouch units per master case. Keep in a cool, dry place.
Undeclared allergens: Milk and Soy
- 2026-07-01FDA-FoodGeorge J Howe Company, Inc.Class IGeorge J Howe sunflower seeds recalled for undeclared cashew
George J Howe Company is recalling 25-pound bags of sunflower seeds because they contain cashew, a tree nut allergen that is not listed on the label. People with cashew allergies could have a serious reaction if they consume this product.
- 2026-07-01FDA-FoodGeorge J Howe Company, Inc.Class IGeorge J Howe sunflower seeds recalled for undeclared cashew
George J Howe Company's 5# sunflower seed products contain cashew, a tree nut allergen that is not listed on the label. People with cashew or tree nut allergies could have a serious allergic reaction if they consume this product.
- 2026-07-01FDA-FoodGeorge J Howe Company, Inc.Class IGeorge J Howe sunflower seeds recalled for undeclared cashew
George J Howe Company is recalling 5-pound bags of sunflower seeds because they contain cashew, a tree nut allergen that is not declared on the label. People with cashew allergies could have a serious allergic reaction if they eat this product.
- 2026-07-01FDA-FoodGeorge J Howe Company, Inc.Class IGeorge J Howe sunflower seed recalled for undeclared cashew
George J Howe Company recalled its 8/9.5 oz Tub Nut sunflower seed products because they contain cashew, a tree nut allergen that is not listed on the label. People with cashew or tree nut allergies could have a serious allergic reaction if they eat this product.
- 2026-07-01FDA-FoodGeorge J Howe Company, Inc.Class IGeorge J Howe sunflower seeds recalled for undeclared cashew
George J Howe Company is recalling 6/11oz No Salt Sunflower Seeds because they contain cashew, a tree nut allergen that is not declared on the label. People with cashew allergies who eat this product could have a serious allergic reaction.
- 2026-07-01FDA-FoodGeorge J Howe Company, Inc.Class IGeorge J Howe sunflower seeds recalled for undeclared cashew
George J Howe Company's 6/11oz Sunflower Seeds Salted contain cashew, a tree nut allergen that is not listed on the label. People with tree nut allergies who eat this product could have a serious allergic reaction.