Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Allura Xper FD10C; System Code: 722001;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1659-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
MEDLINE ANTERIOR HIP PACK DYNJ64672B
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
|
FDA
Z-1711-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 16, 2026
|
Details |
|
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
|
FDA
Z-1744-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 13, 2026
|
Details |
|
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
|
FDA
Z-1654-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Jan 29, 2026
|
Details |
|
Vue Motion V12. Product Number: 1017979.
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
|
FDA
Z-1692-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 5, 2026
|
Details |
|
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1678-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1663-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.
Potential for attenuation degradation over time, decreasing the lifespan.
|
FDA
Z-1758-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 11, 2026
|
Details |
|
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microw
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
|
FDA
Z-1700-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Dec 9, 2025
|
Details |
|
Burlington Medical, Kilt
Potential for attenuation degradation over time, decreasing the lifespan.
|
FDA
Z-1755-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 11, 2026
|
Details |
|
Allura Xper FD20/20; System Code: 722038;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1669-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
Allura Xper FD20/15; System Code: 722058;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1671-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
|
FDA
Z-1646-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 2, 2026
|
Details |
|
Burlington Medical, Caps.
Potential for attenuation degradation over time, decreasing the lifespan.
|
FDA
Z-1760-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 11, 2026
|
Details |
|
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
|
FDA
Z-1708-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 16, 2026
|
Details |
|
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Surgical light assembly may not adequate support the weight of the ceiling cover.
|
FDA
Z-1688-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 23, 2026
|
Details |
|
ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1667-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
Burlington Medical, Thyroid Shield.
Potential for attenuation degradation over time, decreasing the lifespan.
|
FDA
Z-1753-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 11, 2026
|
Details |
|
eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
|
FDA
Z-1731-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 2, 2026
|
Details |
|
ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1662-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
|
FDA
Z-1742-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 13, 2026
|
Details |
|
Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and pl
Due to increased complaints for broken/frayed grip cables for reusable instruments.
|
FDA
Z-1697-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Dec 9, 2025
|
Details |
|
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
|
FDA
Z-1693-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 18, 2026
|
Details |
|
Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251502 Product Description: 5 French sheath, 0.014" guidewire compatible over-the-wire injectable angioplasty balloon catheter, balloon diameter 2.5mm, balloon length 225mm, catheter working length 150cm Component: NA
Potential for the balloon in the device to not meet burst specifications.
|
FDA
Z-1704-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Jul 21, 2025
|
Details |
|
Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TFL-CSLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tissue with moderate hemostasis, little charring, and a thin zone of necrosis. Component: No
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable. Additionally, smoke or a burning smell may occur. By design, the issue causing the smoke or burning smell would be contained within the internal laser console enclosure and would be self-extinguishing.
|
FDA
Z-1695-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 27, 2026
|
Details |
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.
The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.
Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.
Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.