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 1130111320 of 28,172 recalls

Medical DeviceJuly 15, 2020· Qiagen Sciences LLC

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA Recalled by Qiagen...

The Issue: There is an increased rate of potential false positive results for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Stimwave Technologies Inc

Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US -...

The Issue: The product contains a non-functional component not in product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Stimwave Technologies Inc

Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US -...

The Issue: The product contains a non-functional component not in product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Stimwave Technologies Inc

Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-RCV-AO US...

The Issue: The product contains a non-functional component not in product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Stimwave Technologies Inc

Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US...

The Issue: The product contains a non-functional component not in product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Stimwave Technologies Inc

Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-TRL-BO US...

The Issue: The product contains a non-functional component not in product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Stimwave Technologies Inc

Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US -...

The Issue: The product contains a non-functional component not in product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· NeuroLogica Corporation

Recalled Item: OmniTom Computed tomography x-ray system Recalled by NeuroLogica Corporation...

The Issue: There are potential issues related to the operational state of the scanner,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2020· Thomas Scientific

Recalled Item: Wuxi Nest Recalled by Thomas Scientific Due to The firm is replacing all...

The Issue: The firm is replacing all tubes that were manufactured and distributed prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha (VA20) - Model: 10308191 Cios Alpha (VA30) - Recalled by Siemens...

The Issue: Hardware error- Hot Plugging feature could cause an electrical malfunction...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· Aesculap Implant Systems LLC

Recalled Item: ENNOVATE MIS REMOVALKEY SHORT Recalled by Aesculap Implant Systems LLC Due...

The Issue: Fracture or breakage of the spinal fixation arm at the downtube instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides (ALKP is not affected)...

The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· OraSure Technologies, Inc.

Recalled Item: Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2...

The Issue: Incorrect lot number for Standard Oral Fluid Negative Calibrator on...

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

Class III — Low RiskOngoing
Medical DeviceJuly 13, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products TBIL Slides- 5 PACK/300 SLDS In vitro Recalled by...

The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products BuBc Slides - in vitro diagnostic use Recalled by...

The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· OraSure Technologies, Inc.

Recalled Item: Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate...

The Issue: Incorrect lot number for Standard Oral Fluid Negative Calibrator on...

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

Class III — Low RiskOngoing
Medical DeviceJuly 9, 2020· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are...

The Issue: Potential risk of brush detachment during cleaning.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· New Wave Endo-Surgical, Corp.

Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...

The Issue: The plastic housing on the device may fracture

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing