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. 2,591 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,591 in last 12 months

Showing 1400114020 of 28,172 recalls

Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth...

The Issue: An Ad-Tech Clinical Specialist, attended a case on April 15, 2019. During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2019· Zimmer Surgical Inc

Recalled Item: Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece...

The Issue: Foreign Material in the Alvarado Knee Holder Base Plate Assembly and Foot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2019· Med Tec Inc

Recalled Item: CIVCO Solstice(TM) SRS Immobilization System Recalled by Med Tec Inc Due to...

The Issue: There is a potential for movement of the Solstice Tilting Head Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity c Cuvette Segments Recalled by Abbott Gmbh & Co. KG Due to...

The Issue: Individual cuvettes within the Alinity c Cuvette Segment may become seated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2019· Bard Peripheral Vascular Inc

Recalled Item: BD WAVELINQ 4F EndoAVF System Recalled by Bard Peripheral Vascular Inc Due...

The Issue: The firm has become aware of a potential problem with their venous and...

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

Class II — Potential Health HazardOngoing