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. 2,476 recalls have been distributed to Mississippi in the last 12 months.
Showing 23661–23680 of 28,172 recalls
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...
The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....
The Issue: There was an error in manufacturing which resulted in the proximal lag screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor Recalled...
The Issue: The blood pressure (BP) circuit occasionally fails to inflate the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panthera-Puncher 9 . Panthera-Puncher 9 is a sample transfer instrument...
The Issue: Risk of incorrect results from samples prepared with Panthera-Puncher 9
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem 38 mm (1-1/2 Inch) Recalled by...
The Issue: Zimmer is initiating a voluntary recall of 20 production lots of Moore Hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IP5 Information Portal The Expression Information Portal (Model IP5)...
The Issue: The wireless function of the IP5 radio could be interrupted causing loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to There is a possibility the handle...
The Issue: There is a possibility the handle of the laryngoscope may heat up and melt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...
The Issue: STERIS has identified that deformation of the washers door handle pin may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHAROS Excimer Laser Recalled by Ra Medical Systems Inc Due to RA Medical...
The Issue: RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo Imaging XS Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens has become aware of the potential malfunction when using syngo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...
The Issue: The Life Force chamber is marketed and promoted as a medical device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Data Manager 2.0 (Content manager 2.0 Recalled by Brainlab AG Due to...
The Issue: The following defects have been identified for data loaded with Patient Data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The STERIS 4085 General Surgical Table Product Usage: is an Recalled by...
The Issue: STERIS engineering analysis has determined the D1 pressure switch in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...
The Issue: Using the PA230E transducer with a user-defined setting with the output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.