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. 2,558 recalls have been distributed to Mississippi in the last 12 months.
Showing 16821–16840 of 28,172 recalls
Recalled Item: Arrow Multi Lumen CVC Kit (Central venous catheter) Recalled by Arrow...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter) Recalled by...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheterization Kit with Blue FlexTip Catheter Recalled by...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGB+ Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep...
The Issue: Custom surgical kits contain Aplicare Povidone Iodine Prep Pads which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage:...
The Issue: For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A1 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...
The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.