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 92419260 of 28,172 recalls

Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Screw Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek SmartView Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Bard Peripheral Vascular Inc

Recalled Item: Recalled by Bard Peripheral Vascular Inc Due to Potential for needle...

The Issue: Potential for needle protector to become fully dislodge exposing infusion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Contamac Solutions, Inc.

Recalled Item: Nutrifill Scleral Recalled by Contamac Solutions, Inc. Due to Foreign Object...

The Issue: Contact lens solution may contain foreign material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: FaStep COVID-19 IgG/IgM Rapid Test Device Qualitative detection and...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: Status COVID-19/Flu Rapid Immunoassay for Direct Detection and Differential...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma)...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2021· Versea Diagnostics LLC

Recalled Item: CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of...

The Issue: Products may have been distributed to customers other than laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment SP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment NP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment WP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment MU Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment SU Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment PCA Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module clinical chemistry and immunoassay...

The Issue: Due to potential performance issues with software version 3.2.3 and earlier....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Recalled by Philips Respironics, Inc. Due to Two...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Two software...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing