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. 2,614 recalls have been distributed to Mississippi in the last 12 months.
Showing 11781–11800 of 28,172 recalls
Recalled Item: Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product...
The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oscar 2 Recalled by Suntech Medical, Inc. Due to The device display, when...
The Issue: The device display, when activated, can show an incorrect decimal point when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....
The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: Recalled...
The Issue: One (1) TRUE METRIX AIR blood glucose meter distributed in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are...
The Issue: Internal Paddles may wear over time and may not be safe or ready for use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B Recalled by...
The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Professional Urine Drug Control Recalled by Cardinal Health Inc. Due to...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS...
The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-Hydroxybutyrate LiquiColor Recalled by Cardinal Health Inc. Due to Three...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strep B Carrot Broth One-Step Recalled by Cardinal Health Inc. Due to Three...
The Issue: Three products requiring storage conditions were incorrectly stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha VA30-mobile X-Ray system Recalled by Siemens Medical...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Alpha VA20-mobile X-Ray system Material # 10308191 The Recalled...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Cios Spin VA30-mobile X-Ray system Recalled by Siemens Medical...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrysof Recalled by Alcon Research LLC Due to Incorrect IOL diopter
The Issue: Incorrect IOL diopter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Low Weight-Low Volume Blood Transport System for...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Blood Set Prime Line - Product Usage: is Recalled by Baxter...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Blood Transport System for Hemodialysis Blood Set -...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gambro Cartridge Low Volume Blood Transport System for Hemodialysis Blood...
The Issue: Potential disconnection of tubing set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 154335 Oxford Partial Knee System Recalled by Biomet, Inc....
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 184762 Knees Vanguard Knee System Recalled by Biomet, Inc....
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.