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Latest Product Recalls Today

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.

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Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.

Recent Product Recall Alerts List

Showing 2,651 - 2,675 of 3,321 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
FDA Z-1346-2026
Medical Device High
Feb 18, 2026 Recall: Jan 26, 2026
Details
Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710FJ282CRH;
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
FDA Z-1319-2026
Medical Device High
Feb 18, 2026 Recall: Dec 22, 2025
Details
Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
FDA Z-1349-2026
Medical Device High
Feb 18, 2026 Recall: Jan 26, 2026
Details
Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit
A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
FDA Z-1312-2026
Medical Device High
Feb 18, 2026 Recall: Dec 24, 2025
Details
Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
FDA Z-1348-2026
Medical Device High
Feb 18, 2026 Recall: Jan 26, 2026
Details
FDA Z-1320-2026
Medical Device High
Feb 18, 2026 Recall: Dec 22, 2025
Details
Spectral CT; Product Code (REF): 728333;
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
FDA Z-1317-2026
Medical Device High
Feb 18, 2026 Recall: Jan 7, 2026
Details
Brilliance iCT; Product Code (REF): 728306;
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
FDA Z-1315-2026
Medical Device High
Feb 18, 2026 Recall: Jan 7, 2026
Details
Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
FDA Z-1358-2026
Medical Device High
Feb 18, 2026 Recall: Jan 20, 2023
Details
Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576; 2) CENTRAL LINE TRAY W/ CHLRP SWB, Kit SKU RWM-DC57KC.
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
FDA Z-1331-2026
Medical Device High
Feb 18, 2026 Recall: Dec 24, 2025
Details
Surepulse VS Cap Large REF: SP-162-A1 component of VS Newborn Heart Rate Monitor
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
FDA Z-1359-2026
Medical Device High
Feb 18, 2026 Recall: Jan 20, 2023
Details
Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11,3, 11.4 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This may result in a treatment plan that potentially irradiates the incorrect patient location if the error is not detected by users.
FDA Z-1340-2026
Medical Device High
Feb 18, 2026 Recall: Dec 12, 2025
Details
FDA H-0487-2026
Food High
Feb 18, 2026 Recall: Jan 6, 2026
Details
FDA H-0502-2026
Food High
Feb 18, 2026 Recall: Apr 30, 2025
Details
FDA H-0506-2026
Food High
Feb 18, 2026 Recall: Jan 6, 2026
Details
FDA H-0507-2026
Food High
Feb 18, 2026 Recall: Jan 6, 2026
Details
FDA H-0491-2026
Food High
Feb 18, 2026 Recall: Jan 31, 2026
Details
FDA H-0492-2026
Food High
Feb 18, 2026 Recall: Jan 12, 2026
Details
FDA H-0508-2026
Food High
Feb 18, 2026 Recall: Jan 6, 2026
Details
FDA H-0497-2026
Food High
Feb 18, 2026 Recall: Jan 13, 2026
Details
FDA H-0496-2026
Food High
Feb 18, 2026 Recall: Jan 22, 2026
Details
FDA H-0485-2026
Food High
Feb 18, 2026 Recall: Jan 6, 2026
Details
FDA H-0493-2026
Food High
Feb 18, 2026 Recall: Jan 12, 2026
Details
FDA H-0505-2026
Food High
Feb 18, 2026 Recall: Jan 6, 2026
Details
FDA H-0494-2026
Food High
Feb 18, 2026 Recall: Jan 8, 2026
Details
Showing 2,651 - 2,675 of 3,321 product recalls

Product Recalls Today

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CPSC

Latest Consumer Product Recalls

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FDA

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USDA FSIS

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FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.

NHTSA

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Prioritize High-Risk Notices

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Latest Product Recalls FAQ

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Why do some recent recalls have older recall dates?

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.

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Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.

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Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.