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. 2,617 recalls have been distributed to Mississippi in the last 12 months.
Showing 10461–10480 of 28,172 recalls
Recalled Item: Remel Blood Agar/MacConkey Agar Bi-Plate Recalled by Remel Inc Due to The...
The Issue: The blood agar side of the bi-plate may not grow some patient isolates or QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clerio Vision Recalled by Clerio Vision Due to One lot of contact lenses...
The Issue: One lot of contact lenses labeled as BC MED, DIA 14.0 PWR -2.25 contained BC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment Delivery System with iDMS - Product Usage: used...
The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System - Product Usage: used as an integrated Recalled...
The Issue: "MLC tickle error" may result in the delivered dose to effectively rotate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system Recalled by...
The Issue: After the user selects the Lock-in command, the kV and mA values are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-107: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-108: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-108: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix" PMIC-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-105: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-107: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas pro integrated solutions (cobas pro ISE Recalled by Roche...
The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-110: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.