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. 2,614 recalls have been distributed to Mississippi in the last 12 months.
Showing 11461–11480 of 28,172 recalls
Recalled Item: Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage:...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric R1 Buffer - Product Usage: Recalled...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Recalled...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InnoWave Sonic Irrigator Recalled by Steris Corporation Due to A recent FDA...
The Issue: A recent FDA inspection at the firm identified that the foil test performed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America, LLC...
The Issue: The device may experience an interruption of gas measurement due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepIT Q2A Kit Recalled by DNA Genotek Inc. Due to Reagents were shipped to...
The Issue: Reagents were shipped to customers after the Use by data indicated on its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew T-F1X0 RCG Drill Pac Recalled by Smith & Nephew, Inc. Due to...
The Issue: The T-Fix sterile package contains only one sleeve instead of two, The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite with software versions syngo.via VB30 or VB40...
The Issue: If the user modifies for any reason (e.g. reduction of artifacts) the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Radial Pink Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re...
The Issue: The label on the cardbox and the blister show the correct symbols for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Radial Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Black Starshine Recalled by Chengdu Ai Qin E-commerce Co.,...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Devil Red Recalled by Chengdu Ai Qin E-commerce Co., Ltd Due...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Diamonds Starlight Recalled by Chengdu Ai Qin E-commerce Co.,...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Flower Grey Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TTDEYE (brand) Flower Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo.CT VB20 or VB20_SP1 in the following systems:...
The Issue: Sporadic problems with the current software may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARTO 3 System (Software Version V7.1.80) Recalled by Biosense Webster...
The Issue: Software defect may result in disapperance of tag sites during recalculation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE ONE Recalled by GE Healthcare, LLC Due to CARESCAPE ONE may not...
The Issue: CARESCAPE ONE may not provide visual and audible alarms for Ventricular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray System Recalled by Shanghai United Imaging...
The Issue: The metal edge overlap of the mylar strip in the gantry was uneven, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.