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. 2,394 recalls have been distributed to Mississippi in the last 12 months.
Showing 43261–43280 of 49,744 recalls
Recalled Item: Propofol Injectible Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Glass defect located on the interior neck of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candy Sweet Spots Recalled by Bee International, Inc. Due to Undeclared Egg
The Issue: Bee International is recalling Sweet Spots Candy because it has undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VirtuoSaph¿ Plus Endoscopic Vessel Harvesting System Recalled by Terumo...
The Issue: Sterility of medical devices intended for use in surgical procedures may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade Kit Recalled by GE Healthcare Due to Medical device adjustment knob...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stand-Alone Resuscitation Unit Recalled by GE Healthcare Due to Medical...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panda iRes¿ Infant Warmers Recalled by GE Healthcare Due to Medical device...
The Issue: Medical device adjustment knob may be loose and affect the accuracy of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is Recalled...
The Issue: On December 13, 2012, King Systems initiated a voluntary recall of one (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrOXYzine HCI Tablets USP 10 mg Recalled by KVK-Tech, Inc. Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrOXYzine HCI Tablets USP 25 mg Recalled by KVK-Tech, Inc. Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrOXYzine HCI Tablets USP 50 mg Recalled by KVK-Tech, Inc. Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic Slim capsules (Ling Zhi Recalled by Slim Beauty USA Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Ming's Chinese Capsule (Ginger 50 mg Recalled by Slim Beauty USA Due to...
The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dream Body Slimming Capsule (Chinese bitter orange 24% Recalled by Slim...
The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: External Implant RBT Recalled by BioHorizons Implant Systems Inc Due to The...
The Issue: The body length of the External Implant 40105D3 Lot 1302762 labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator with CO2/EtCO2 Measurement The...
The Issue: MRx defibrillator displays a -?- for EtCO2 and does not display EtCO2 values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.