Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,623 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,623 in last 12 months

Showing 83018320 of 28,172 recalls

Medical DeviceFebruary 28, 2022· Respironics California, LLC

Recalled Item: Philips Respironics V680 Ventilator (All Models Recalled by Respironics...

The Issue: Ventilator units have an issue impacting an internal electrical circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 28, 2022· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator (All Models Recalled by Respironics...

The Issue: Ventilator units have an issue impacting an internal electrical circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 28, 2022· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator (All Models Recalled by Respironics...

The Issue: Ventilator units have an issue impacting an internal electrical circuit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 28, 2022· Integra LifeSciences Corp.

Recalled Item: Integra Universal Flexible Arm part number Recalled by Integra LifeSciences...

The Issue: Excess force used to tighten the Universal Flexible Arm can cause the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Philips North America Llc

Recalled Item: DigitalDiagnost C50 1.1 Recalled by Philips North America Llc Due to...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Application software VE20 (Material Number 10848815) installed on the...

The Issue: After CT image data from Toshiba is loaded, image mirroring can occur along...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono floor in combination with a Siemens Healthineers table Recalled...

The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono biplane- in combination with a Siemens Healthineers table...

The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis pheno- in combination with a Siemens Healthineers table or Recalled by...

The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: Product is mislabeled as self-righting Luer slip tip caps, yellow.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Anterior Hip Pack - Surgical Kit Recalled by Stradis Medical, LLC dba...

The Issue: The outer bag may be perforated or torn, which may result in a breach in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Coryell Memorial Hosp Total Recalled by Stradis Medical, LLC dba Stradis...

The Issue: The outer bag may be perforated or torn, which may result in a breach in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Surgicare Neuro Pack - Neurological Kit Recalled by Stradis Medical, LLC dba...

The Issue: The outer bag may be perforated or torn, which may result in a breach in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Total Knee Pack - Surgical Kit Recalled by Stradis Medical, LLC dba Stradis...

The Issue: The outer bag may be perforated or torn, which may result in a breach in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Lum Lam Custom Pack - Anesthesia Kit Recalled by Stradis Medical, LLC dba...

The Issue: The outer bag may be perforated or torn, which may result in a breach in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Baxter Healthcare Corporation

Recalled Item: MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S Recalled by...

The Issue: Devices distributed lacked regulatory clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Brainlab AG

Recalled Item: ExacTrac Dynamic software model numbers: 20910-01 Recalled by Brainlab AG...

The Issue: The yaw angle may be incorrect for CBCT positioning workflows using setup...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· International Science & Technology, LP, DBA Diamatrix Ltd.

Recalled Item: Outer Packaging Label: Protekt Sharps Safety Knives - 44620MU Recalled by...

The Issue: Surgical knives may contain incorrect description printed on handles....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR Vue System Recalled by Boston Scientific Corporation Due to Users...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing