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. 2,591 recalls have been distributed to Mississippi in the last 12 months.
Showing 14521–14540 of 28,172 recalls
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...
The Issue: Potential for tampon to come apart upon removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed Recalled by ProSun...
The Issue: ProSun International LLC discovered discrepancies in their Quality Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProSun V3 42 Xlc(160w)(10 minutes) tanning bed Recalled by ProSun...
The Issue: ProSun International LLC discovered discrepancies in their Quality Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius Knee Cemented Tibial Component Product Usage: Knee replacement...
The Issue: Product mix up
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement...
The Issue: Product mix up
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN):...
The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Atellica IM aTG (100 test kit) Siemens Material Number (SMN):...
The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM aTG (500 test kit) Siemens Material Number (SMN): 10995462...
The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur aTG (100 test kit) Siemens Material Number Recalled by...
The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK STEM with Microporous Surface MP Reconstruction Prosthesis Recalled by...
The Issue: The reaming guide and the guide rod can't be screwed into the intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROXIMATE¿ PPH Hemorrhoidal Circular Stapler Product Code:PPH03 PPH03: The...
The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROXIMATE¿ HCS Hemorrhoidal Circular Stapler Product Code: PPH01 PPH01: The...
The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VisuMax Software Version 2.10.13 with activated Software-Module ReLEx...
The Issue: VisuMax devices with software version 2.10.13 and activated SW-Module ReLEx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Adapter Percutaneous Pin Recalled by Medtronic Navigation, Inc....
The Issue: Under certain circumstances, the percutaneous pin adapter used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon DUALSTOP Red Cap used for intravascular lines Product Code: Recalled...
The Issue: DualStop Caps defect causing leaks in affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vyon DUALSTOP White Cap used for intravascular lines Product Code: Recalled...
The Issue: DualStop Caps defect causing leaks in affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature...
The Issue: Some SureStep" Foley Tray Systems with product catalog number A319418AM and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-View¿ Contrast Enhanced Digital Mammography Recalled by Hologic, Inc. Due...
The Issue: Calibration issue not possible to visualize contrast uptake in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.