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.
Showing 13561–13580 of 28,172 recalls
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...
The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...
The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Cycler Cassettes (a disposable cassette that is intended to Recalled...
The Issue: Additional Instructions: step-by step handling and inserting the cassette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratus CS Acute Care cTNI TestPak Recalled by Siemens Healthcare...
The Issue: Potential for increased rate of false positive results and/or increased rate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPi-Sense Guided Coagulation System with Visitrax Recalled by AtriCure, Inc....
The Issue: The sterile package seal for the Epi-Sense Guided Coagulation System may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healing Abutment Conical Connection RP 0 3.6 x 5mm Recalled by Nobel Biocare...
The Issue: Packaged dental implant healing abutments were found to contain the wrong...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 6 Fr 1.5 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ICS CHARTR EP 200 Recalled by GN Otometrics Due to There is a risk to...
The Issue: There is a risk to the healthcare professional or patient of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229036A...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A...
The Issue: The potential sporadic performance problems may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Crosslock ePAK Screw Driver Recalled by Zimmer Biomet, Inc. Due to There...
The Issue: There is a potential for weak seals of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Crosslock ePAK Depth Gauge Recalled by Zimmer Biomet, Inc. Due to There...
The Issue: There is a potential for weak seals of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Trochar Tip Recalled by Zimmer Biomet, Inc. Due to There is a...
The Issue: There is a potential for weak seals of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.