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. 2,619 recalls have been distributed to Mississippi in the last 12 months.
Showing 10141–10160 of 28,172 recalls
Recalled Item: Custom Perfusion System (CUSTOM PACK BB7W03R8 CCSM NEON). The Affinity...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion Pack (CUSTOM PACK HY11B40R1 1/4 RESPIRATO). The...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Affinity Pixie BP241 Hollow Fiber Oxygenator and Cardiotomy/Venous...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Perfusion System (CUSTOM PACK BB10H89R4 ECLR). The Affinity Pixie...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Affinity Pixie Hollow Fiber Oxygenator and Cardiotomy/Venous...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable cardioverter defibrillators (ICD) with cardiac resynchronization...
The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coronavirus antigen detection test system - Product Usage: intended for...
The Issue: Two lots of test strips failed QC testing using blank buffer due to false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR...
The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista HDLC - colorimetric method Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America Llc Due to...
The Issue: Manufacturing failed to follow process steps resulting in the distribution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Ophthalmic Surgical Procedure Packs Recalled by Alcon Research,...
The Issue: Reports have been received concerning mold found on gowns included in custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Feth-R-Kath Catheter Recalled by Epimed International, Inc. Due to Outer...
The Issue: Outer coating of the catheter may deteriorate and result in the coating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velocity Disposable Bipolar Ablators - Product Usage: intended to be...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Disposable Bipolar Ablators - Product Usage: intended to be Recalled...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HNM Disposable Bipolar Ablators - Product Usage: intended to be used for...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Series Equipment Management System Recalled by Stryker Communications Due...
The Issue: The manufacturer has become aware that there is a likelihood that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia gas-machine - Product Usage: intended for use in administering...
The Issue: Maquet Critical Care AB received complaints where the FiCO2 value was not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (N) 180-Drager Breathing Circuits/Anesthesia Sets Order...
The Issue: Y-piece may become detached from the ventilation hose either before or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.