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. 2,489 recalls have been distributed to Mississippi in the last 12 months.
Showing 21621–21640 of 28,172 recalls
Recalled Item: Perfectum Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro-Mate Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Electrical Clipper with Charging base The Electrical Surgical...
The Issue: Charging base of surgical clippers overheats and smokes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4C Occiput Torque Wrench F/Set Screw Recalled by Aesculap, Inc. Due to A...
The Issue: A FW103R torque wrench that was improperly reassembled after reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX850 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce GX540 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX650 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE Body Coil 1.5T with identification Recalled by Philips Electronics...
The Issue: Wrong positioning of the coil cables can create unintended resonances via...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmer and Infant Gel Warmer Recalled by CooperSurgical, Inc....
The Issue: Product marketed without a 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Potential...
The Issue: Potential issue leading to data loss and patient data mix-up
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actuator for angiographic x-ray monitor ceiling suspension system. Actuator...
The Issue: The actuator assembly became detached and the monitor carriage with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicICE v 2.3.14 nordicICE is an image processing software package...
The Issue: The bug causes BOLD activation maps to be visualized as overlays without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.