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 |
|---|---|---|---|---|---|
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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 |
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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
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FDA
Z-1319-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 22, 2025
|
Details |
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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 |
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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
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Details |
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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 |
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Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH; Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81483RH; Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81102RH 81104RH 81174RH 81531RH 81532RH; Inquiry Steerable Diagnostic Catheter 10 Elec. 5mm 81107RH; Inquiry Steerable Diagnostic Catheter 4 Elec. 2-5-2mm 81402RH 81404RH 81405RH 81474RH; Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81473RH
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-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
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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
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Medical Device | High |
Feb 18, 2026
Recall: Jan 7, 2026
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Details |
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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 |
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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
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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 |
|
Carrot Top Kitchens White Truffle Hummus; contains chickpeas, tahini, truffle oil, lemon, salt; 8 oz.
Contains undeclared sesame
|
FDA
H-0487-2026
|
Food | High |
Feb 18, 2026
Recall: Jan 6, 2026
|
Details |
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CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS, ROSEMONT, IL 60018; PEANUT BUTTER NET WT. 0.5OZ & NET WT 0.75OZ DIST BY: DYMA BRANDS, INC. ATLANTA, GA 30328; Product also sold under the following brand names: FLAVOR Fresh PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY: DYMA BRANDS, INC. ATLANTA, GA 30328; HOUSE RECIPE CREAMY PEANUT BUTTER NET WT 0.75 OZ (21.2g) DISTRIBUTED BY SYSCO COROPRATION, HOUSTON, TEXAS 77077; Katy's Kitchen SMOOTH PEANUT BUTTER NET WT 0.75 OZ (21g) MARKETED BY INDEPENDENT MARKETING ALLIANCE HOUSTIN, TX 77043 PEANUT BUTTER creamy NET WT 0.75 OZ (21g)
Foreign material. During production, the firm found pieces of blue plastic in a filter.
|
FDA
H-0502-2026
|
Food | High |
Feb 18, 2026
Recall: Apr 30, 2025
|
Details |
|
Karison brand PUNJABI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00215 4; Distributed By: Karison Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Product contains milk, which is undeclared in the ingredient statement.
|
FDA
H-0506-2026
|
Food | High |
Feb 18, 2026
Recall: Jan 6, 2026
|
Details |
|
Karison brand NO SUGAR ADDED BESAN LADDOO; Ingredients: Gram Flour, Butter, Zero Trans Fat Vegetable Shortening (Hydrogenated Soybean Oil), Pistachio, Almonds, Sweetener with Nutrasweet; UPC: 8 97397 00221 5; Distributed By: Karison Foods & Snacks, Inc, 34 Willowdale Ave., Port Washington, N.Y. 11050; NET WT. 12 oz.; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Product contains milk, which is undeclared in the ingredient statement.
|
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 | |
|
Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly bag (6/5 lb bags), Net Wt. 30 lbs (13.6 kg)/ case. UPC on 30 lbs case label: 1 00 72714 00215 8. Manufactured by McCain Foods USA Inc. McCain distributed this product to foodservice accounts and product was not sold at retail stores.
Foreign material (small hard plastic fragments).
|
FDA
H-0492-2026
|
Food | High |
Feb 18, 2026
Recall: Jan 12, 2026
|
Details |
|
Karison brand ALSI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar Flax Seeds, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00251 2; Distributed By: Karison Foods & Snacks Inc.; 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Product contains milk, which is undeclared in the ingredient statement.
|
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 | |
|
Karison brand BESAN LADDOO; NET WT. 12 oz.; Ingredients: Gram Flour, Butter, Sugar, Zero Trans Fat Vegetable Shortening, Almonds, Cardamom; UPC: 8 9730700240 6; Distributed By: Karson Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Product contains milk, which is undeclared in the ingredient statement.
|
FDA
H-0505-2026
|
Food | High |
Feb 18, 2026
Recall: Jan 6, 2026
|
Details |
|
Smoked Grouper Dip 7lb plastic tub with tamper proof lid 1/7lb tub per case. Keep Refrigerated.
Undeclared Milk, Eggs, Sodium metabisulfite
|
FDA
H-0494-2026
|
Food | High |
Feb 18, 2026
Recall: Jan 8, 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.