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. 2,448 recalls have been distributed to Mississippi in the last 12 months.
Showing 30601–30620 of 49,744 recalls
Recalled Item: Philips Healthcare Ingenuity Core128 X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance 64 System Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance iCT SP X-Ray Recalled by Philips Electronics...
The Issue: During a bolus tracking procedure, no images were generated when the scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: An error in NVIDIA GPU (Graphics Processing Unit) card drivers can occur for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST XM256 (Cefuroxime) Recalled by BioMerieux SA Due to Potential...
The Issue: Potential performance issues. False Susceptible result instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST NEEDLE 15GA X 2 Intended for the purpose of Recalled by Argon...
The Issue: The recalling firm received a complaint from one of their customers of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN Recalled by Argon Medical...
The Issue: The recalling firm received a complaint from one of their customers of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G Recalled by Argon...
The Issue: The recalling firm received a complaint from one of their customers of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: Clamping the clear tube very close to the blue hub may cause a localized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Duodenoscope These instruments are intended to provide optical...
The Issue: Pentax initiated a field correction/safety alert for two (2) models of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Strata II / Strata NSC Valves (includes Burr Hole Recalled by...
The Issue: Medtronic Neurosurgery initiated a recall after receiving five (5) Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taclonex (calcipotriene and betamethasone dipropionate) Topical Suspension...
The Issue: Labeling: Incorrect or missing package insert: the affected product was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DEXAMETHASONE ELIXIR Recalled by Vintage Pharmaceuticals LLC dba Qualitest...
The Issue: Failed Impurities/ Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5...
The Issue: A portion of this lot of blood collection tubes was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.