Estados Unidos Recalls
Retiros de seguridad del consumidor de la FDA, CPSC, NHTSA y USDA FSIS.
FDA FoodUPC 25312600000 MUFFINS BANANA NUT CREAM CHEESE FILLED 2CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
UPC 25312600000 MUFFINS BANANA NUT CREAM CHEESE FILLED 2CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Contains statement does not declare Walnut
FDA FoodUPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
UPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Contains statement does not declare Salmon and Walnut
FDA DevicesBD Pyxis MedStation 4000 REF: 303 Medication cabinet
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
FDA Food#800414/003729Butter Parsley, Net Wt: 50 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094
#800414/003729Butter Parsley, Net Wt: 50 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094
Products may be potentially contaminated with Salmonella.
FDA DevicesNeptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.
FDA FoodUPC 21843300000 READY MEALS TUNA SALAD & MUENSTER CHEESE SNACK PACK This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
UPC 21843300000 READY MEALS TUNA SALAD & MUENSTER CHEESE SNACK PACK This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Contains statement does not declare Tuna
FDA DevicesCovidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044
Temperature probe devices lack FDA clearance.
FDA DevicesBrand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: No
Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: No
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
FDA FoodUPC 27841000000 Ready Meals TRAY BRIE & BLEU CHEESE LARGE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
UPC 27841000000 Ready Meals TRAY BRIE & BLEU CHEESE LARGE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Contains statement does not declare Almond
NHTSADenago EV Corporation - Missing Pedestrian Warning Sounds/FMVSS 141
Denago EV Corporation - Missing Pedestrian Warning Sounds/FMVSS 141
A vehicle that does not emit sound may fail to alert pedestrians of a moving vehicle, increasing the risk of a crash or injury.
FDA DevicesLVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless it is reconnected to AC mains power.
FDA DevicesCASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charring or discoloration of thermal printer paper. Ignition of the paper could potentially result in serious thermal injury.
FDA FoodUPC 23152800000 SHRIMP 41-50 P&D With JAMAICAN JERK MARINADE 5% This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
UPC 23152800000 SHRIMP 41-50 P&D With JAMAICAN JERK MARINADE 5% This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Contains statement does not declare Shrimp.
FDA FoodUPC 28586600000 CROISSANT ALMOND UPC 22102100000 CROISSANTS ALMOND 4 CT UPC 29671400000 HGN CROISSANTS ALMOND 3CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
UPC 28586600000 CROISSANT ALMOND UPC 22102100000 CROISSANTS ALMOND 4 CT UPC 29671400000 HGN CROISSANTS ALMOND 3CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Contains statement does not declare Almond
FDA DevicesDigital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D150BC-40 / D150VC-40 / D150LC-40 / D150LC-40E/D150BC-41 / D150VC-41 / D150LC-41; Digital Radiography System RADspeed safire: UD150B-40 / D150BC-40; Radiography System RADspeed fit: N/A (Integrated in the system); X-RAY R/F SYSTEM SONIALVISION safire17:UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION safire Plus: UD150B-40 / D150BC-4;0 X-RAY R/F SYSTEM SONIALVISION safire: UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION VERSA: UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM FLUOROspeed 300:UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM SONIALVISION G4:D150BC-40S; X-RAY R/F SYSTEM FLUOROspeed X1:D150BC-40S
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D150BC-40 / D150VC-40 / D150LC-40 / D150LC-40E/D150BC-41 / D150VC-41 / D150LC-41; Digital Radiography System RADspeed safire: UD150B-40 / D150BC-40; Radiography System RADspeed fit: N/A (Integrated in the system); X-RAY R/F SYSTEM SONIALVISION safire17:UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION safire Plus: UD150B-40 / D150BC-4;0 X-RAY R/F SYSTEM SONIALVISION safire: UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION VERSA: UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM FLUOROspeed 300:UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM SONIALVISION G4:D150BC-40S; X-RAY R/F SYSTEM FLUOROspeed X1:D150BC-40S
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
FDA DevicesPhilips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
FDA DevicesBD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
FDA DevicesMAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph
MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph
Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. This could impact clinical decision-making.
FDA DrugsLidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520. NDC: 55150-164-02
Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520. NDC: 55150-164-02
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
FDA DevicesPhilips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
FDA DevicesAtlan A350. Model Number: 8211500. anesthesia workstation
Atlan A350. Model Number: 8211500. anesthesia workstation
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
FDA FoodUPC 29502200000 Ready Meals BOWL GRAIN SALMON QUINOA LENTIL SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
UPC 29502200000 Ready Meals BOWL GRAIN SALMON QUINOA LENTIL SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Contains statement does not declare Salmon
FDA DevicesBD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
FDA DevicesDeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
Sterile wound dressing, lacks sterility assurance