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 16161–16180 of 28,172 recalls
Recalled Item: Terumo HX2 Temperature Management System Recalled by Terumo Cardiovascular...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama 1.0T Recalled by Philips Electronics North America Corporation Due...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns TCM II Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Update to cooler-heater cleaning instructions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare: a) Prodigy Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX Duo Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Lunar: a) DPX NT Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a)...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rectal Catheters Recalled by Teleflex Medical Europe Ltd Due to These...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URO-3 Triple Stain (CD44 + p53) with CK20 Recalled by Biocare Medical, LLC...
The Issue: Immunohistochemistry device kits found to display incorrect staining pattern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect simply InterActive Implant Recalled by Implant Direct Sybron...
The Issue: The cap on the vial might be labeled with the incorrect part number but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.