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. 2,590 recalls have been distributed to Mississippi in the last 12 months.
Showing 15881–15900 of 28,172 recalls
Recalled Item: Artis zee MP Recalled by Siemens Medical Solutions USA, Inc Due to After the...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. Sold under the following product names: Recalled...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Revolution EVO Recalled by GE Healthcare Japan Corporation Due...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT540. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Pentra Micro ALBUMIN 2 CP Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: When the ABX Pentra Micro ALBUMIN 2 CP (ALBT2) Reagent 2 is sampled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX SLEEVEGK3 (2) BOX SLEEVEGK4 SLEEVE GASTRECTOMY (3)BOX SLEEVEJAWI...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 60mm -2.5mm...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX PST01199 BARIATRIC TRISTAPLE (Item Number: PST01199) (2) BOX PST03403...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX MGBGLOGX1 ZESTAW MINI GASTRIC BYPASS Product Usage: The Endo Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX KITDE0183 APPENDIX LIPPE DETMOLD (KITDE0183) (2) KIT-DE-0083...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MGBX ZESTAW GB LS X1 Product Usage: The Endo GIA Recalled by COVIDIEN...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm - Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.