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Medical DeviceUSFDA Devices

Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B

Medline Industries, LP
FDA DevicesClass II

Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B

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.

Feb 18, 2026Medline Industries, LP
Food & BeverageUSFDA Food

Karison brand PANJIRI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Almonds, Sugar, Lotus Seeds, Fennel Seeds, Flax Seeds, Edible Gum, Ginger Powder, Zero Trans Fat Vegetable Shortening; UPC: 8 97307 00243 7; 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.

Karison Foods & Snacks, Inc.
FDA FoodClass II

Karison brand PANJIRI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Almonds, Sugar, Lotus Seeds, Fennel Seeds, Flax Seeds, Edible Gum, Ginger Powder, Zero Trans Fat Vegetable Shortening; UPC: 8 97307 00243 7; 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.

Feb 18, 2026Karison Foods & Snacks, Inc.
Medical DeviceUSFDA Devices

Spectral CT; Product Code (REF): 728333;

Philips North America Llc
FDA DevicesClass II

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.

Feb 18, 2026Philips North America Llc
Medical DeviceUSFDA Devices

Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; 3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615; 4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660; 5) CENTRAL LINE DRESSING CHANGE K, Kit SKU DT19665; 6) NEONATAL DRESSING CHANGE KIT, Kit SKU DT21495; 7) NICU CVC DRESSING CHANGE TRAY, Kit SKU DT22510A; 8) DRESSING CHANGE TRAY W/TEG CHG, Kit SKU DYNDC3114B; 9) DRESSING CHANGE KIT, Kit SKU DYNDC3351.

Medline Industries, LP
FDA DevicesClass II

Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; 3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615; 4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660; 5) CENTRAL LINE DRESSING CHANGE K, Kit SKU DT19665; 6) NEONATAL DRESSING CHANGE KIT, Kit SKU DT21495; 7) NICU CVC DRESSING CHANGE TRAY, Kit SKU DT22510A; 8) DRESSING CHANGE TRAY W/TEG CHG, Kit SKU DYNDC3114B; 9) DRESSING CHANGE KIT, Kit SKU DYNDC3351.

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.

Feb 18, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45

Intuitive Surgical, Inc.
FDA DevicesClass II

da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45

Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception) but 2D maintained, or loss of both displays-complete visualization loss, without fault, instruments remain active, could lead to instrument contact with tissue, resulting in injury/bleeding; may require alternate surgical modality.

Feb 18, 2026Intuitive Surgical, Inc.
Medical DeviceUSFDA Devices

Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.

Elekta, Inc.
FDA DevicesClass II

Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 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.

Feb 18, 2026Elekta, Inc.
Medical DeviceUSFDA Devices

Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H

Steris Corporation
FDA DevicesClass II

Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H

This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configuration file was used.

Feb 18, 2026Steris Corporation
Medical DeviceUSFDA Devices

Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor

SUREPULSE MEDICAL LTD
FDA DevicesClass III

Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor

Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.

Feb 18, 2026SUREPULSE MEDICAL LTD
Medical DeviceUSFDA Devices

Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088

Medline Industries, LP
FDA DevicesClass II

Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088

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.

Feb 18, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(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.

Feb 18, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Food & BeverageGermanyGermany BVL

Belvas Easter Eggs Mix Pralines, 100 Gramm

Chocolaterie Belvas SA Chemin du Fundus 7 7822 Ghislenghien Belgien
Germany BVLGeneral Alert

Belvas Easter Eggs Mix Pralines, 100 Gramm

Allergene

Feb 17, 2026Chocolaterie Belvas SA Chemin du Fundus 7 7822 Ghislenghien Belgien
Food & BeverageFranceRappelConso

sans marque - saucisse de veau

sans marque
RappelConsovolontaire (san...

sans marque - saucisse de veau

détection de salmonelles

Feb 17, 2026sans marque
PharmaceuticalUKUK

Class 3 Medicines Recall: Norgine Limited, MOVICOL Ease Citrus Powder for oral solution 13.7 g, EL(26)A/08

Norgine LimitedUK
uk-mhraMedicines Recall

Class 3 Medicines Recall: Norgine Limited, MOVICOL Ease Citrus Powder for oral solution 13.7 g, EL(26)A/08

Norgine Limited is recalling one batch of product as a precautionary measure due to some units containing low amounts of active ingredients....

Feb 17, 2026Norgine Limited
Medical DeviceUKUK

Field Safety Notices: 09-13 February 2026

MHRAUK
uk-mhraMedical Device ...

Field Safety Notices: 09-13 February 2026

A list of Field Safety Notices: 09-13 February 2026...

Feb 17, 2026MHRA
Food & BeverageFranceRappelConso

kerblavet - poitrine roulee fumee cuite*4

kerblavet
RappelConsovolontaire (san...

kerblavet - poitrine roulee fumee cuite*4

présence de listeria monocytogenes

Feb 17, 2026kerblavet
Food & BeverageGermanyGermany BVL

Maissnack der Marke "BOY BAWANG"

Heuschen & Schrouff Oriental Food Trading B.V.
Germany BVLGeneral Alert

Maissnack der Marke "BOY BAWANG"

Allergene

Feb 17, 2026Heuschen & Schrouff Oriental Food Trading B.V.
Safety AlertCanadaHealth Canada

Patchwork and Pine Inc. Lip Balm and Artisan Soap recalled due to the presence of prohibited ingredients

Consumer product safety
Health CanadaGeneral Alert

Patchwork and Pine Inc. Lip Balm and Artisan Soap recalled due to the presence of prohibited ingredients

Chemical hazard

Feb 17, 2026Consumer product safety
Vehicle RecallUSNHTSA

Winnebago Industries, Inc. - Rear Roof Cap May Detach

Winnebago Industries, Inc.
NHTSASTRUCTURE

Winnebago Industries, Inc. - Rear Roof Cap May Detach

A detached roof cap can become a road hazard for other vehicles and increase the risk of a crash.

Feb 17, 2026Winnebago Industries, Inc.
Vehicle RecallUSNHTSA

Prevost Car (US) Inc. - Improperly Installed Passenger Seat Anchors

Prevost Car (US) Inc.
NHTSASEATS

Prevost Car (US) Inc. - Improperly Installed Passenger Seat Anchors

An improperly installed seat anchor may not adequately restrain the seat occupant, increasing the risk of injury during a crash.

Feb 17, 2026Prevost Car (US) Inc.
Vehicle RecallUSNHTSA

Ford Motor Company - High Voltage Battery May Short Circuit

Ford Motor Company
NHTSAELECTRICAL SYSTEM

Ford Motor Company - High Voltage Battery May Short Circuit

Battery failure can cause a loss of drive power, increasing the risk of a crash. Battery failure can also increase the risk of a fire.

Feb 17, 2026Ford Motor Company
Vehicle RecallUSNHTSA

Shyft Group - Gearbox May Bind and Cause Loss of Steering

Shyft Group
NHTSASTEERING

Shyft Group - Gearbox May Bind and Cause Loss of Steering

Binding in the gearbox can cause a loss of steering, increasing the risk of a crash.

Feb 17, 2026Shyft Group
Vehicle RecallUSNHTSA

Ford Motor Company - Do Not Drive - Loss of Brake Function/FMVSS 105

Ford Motor Company
NHTSASERVICE BRAKES,...

Ford Motor Company - Do Not Drive - Loss of Brake Function/FMVSS 105

A loss of brake function increases the risk of a crash.

Feb 17, 2026Ford Motor Company
Food & BeverageFranceRappelConso

chopsticks helper - lion, lapin, tigre, souris, ours, chat chopsticks helper / aide baguette et baguette modèle lion, lapin, souris, ours, chat, tigre.

chopsticks helper
RappelConsovolontaire (san...

chopsticks helper - lion, lapin, tigre, souris, ours, chat chopsticks helper / aide baguette et baguette modèle lion, lapin, souris, ours, chat, tigre.

présence de formaldéhyde et de mélamine en quantités supérieures à la limite légale

Feb 17, 2026chopsticks helper
Food & BeverageFranceRappelConso

sans marque - steaks hachés préparés sur place

sans marque
RappelConsovolontaire (san...

sans marque - steaks hachés préparés sur place

prélèvement aqualeha, identification de listeria.¤

Feb 17, 2026sans marque
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