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. 2,617 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,617 in last 12 months

Showing 1108111100 of 28,172 recalls

Medical DeviceAugust 25, 2020· Medtronic Vascular

Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...

The Issue: Subsequent failure of catheters in the field and failed quality testing

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista Akaline Phosphatase (ALPI) Flex reagent cartridge -...

The Issue: Low outlier resultsgenerated with Alkaline Phosphatase (ALPI) Flex reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Medtronic Vascular

Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...

The Issue: Subsequent failure of catheters in the field and failed quality testing

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2020· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM HER-2/neu (H2n) assay Recalled by Siemens Healthcare...

The Issue: Siemens confirmed that the Upper Limit of Normal (ULN) as claimed in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Genicon, Inc.

Recalled Item: Aquas PowerFlow Tube Set - Product Usage: The device delivers Recalled by...

The Issue: The product design incorporating a motor driven impeller pump powered by one...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Radiology Solutions 14.0 Recalled by CHANGE HEALTHCARE...

The Issue: Software defect which may potentially result in one or more images missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x1/16 UAS BLK...

The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 1/4x3/32 Recalled...

The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Ultrasonic Air Sensor 3/8x3/32 Recalled...

The Issue: Internal testing at the supplier, revealed that a crimped wire was placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Boston Scientific Corporation

Recalled Item: Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) Recalled by...

The Issue: Opticross 35 Peripheral Imaging Catheter is being recalled because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Alcon Research, LLC

Recalled Item: Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health"...

The Issue: The third-party brand latex micro surgical gloves packaged within specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Irvine Biomedical Inc, a St. Jude Medical Co.

Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...

The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Irvine Biomedical Inc, a St. Jude Medical Co.

Recalled Item: Inquiry Steerable Diagnostic Catheter Recalled by Irvine Biomedical Inc, a...

The Issue: Steerable diagnostic catheter packages labeled Model IBI-81104, batch...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2020· Imactis

Recalled Item: Imactis Patient Fiducial (Patient ) Recalled by Imactis Due to The firm has...

The Issue: The firm has received reports concerning the patient fiducial disk...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2020· Handicare AB

Recalled Item: SwiftHook sold as the following: a. Individually as SwiftHook b. Recalled by...

The Issue: Carry bar may detach during use of mobile lifts and ceiling lifts equipped...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2020· North American Rescue LLC.

Recalled Item: 4 In. Flat Responder Emergency Trauma Dressing part number 30-0171 Recalled...

The Issue: Lack of sterility assurance of the 30-0171

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Anti-TPO Assay on cobas e analyzers 411 Recalled by Roche...

The Issue: Recent internal verification studies found the current RF interference claim...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2020· Ansell Healthcare Products LLC

Recalled Item: MICROFLEX Diamond Grip Examination Gloves Recalled by Ansell Healthcare...

The Issue: Examination gloves were shipped inadvertently, without to verify barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension LOCI High Sensitivity Troponin I (TNIH) Flex reagent...

The Issue: Positive bias across the Analytical Measurement Range of the TNIH assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Software: Syngo.via RT Image Suite software version VA30_SP02 with license...

The Issue: Calibration offset between the central CT image plane and the external RT...

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

Class II — Potential Health HazardOngoing