Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,628 recalls have been distributed to Arkansas in the last 12 months.
Showing 6961–6980 of 49,990 recalls
Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...
The Issue: Express chest drains are pre-packaged with sterile water syringes which have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANORO ELLIPTA (umeclidinium and vilanterol inhalation powder) 62.5...
The Issue: Failed Release Testing: Coarse Particle Mass for umeclidinium Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...
The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...
The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion system Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: System may exhibit a loss of imaging functionality and data due to an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Frequency Transport Phasitron Breathing Circuit Kit Recalled by...
The Issue: Due to an assembly error within the breathing circuit, their pressure output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate Recalled by Greiner...
The Issue: Tubes have missing additive/anticoagulant resulting in clotting in most...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertraline Tablets Recalled by Legacy Pharmaceutical Packaging LLC Due to...
The Issue: CGMP Deviations: Inadequate line clearance which may result in a potential...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BrainFeedback Pro 2 Device - is intended as an instrument Recalled by RONAN...
The Issue: Neurofeedback systems removed due to missing design and development...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus/Gyrus Paparrela-Type Vent Tube 1.02MM Recalled by Olympus...
The Issue: The expiration date is missing from the primary (inner) packaging. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System Recalled by Getinge Usa Sales Inc Due to Potential...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill Recalled by Globus Medical, Inc. Due to...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i C20 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill with Stop Recalled by Globus Medical, Inc. Due...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-e Anesthesia System Recalled by Getinge Usa Sales Inc Due to Potential...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical Cranial Drill with Stop Recalled by Globus Medical, Inc. Due...
The Issue: Sterile-packed Cranial Drills may not be sterile due to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i C30 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-i C40 Anesthesia System Recalled by Getinge Usa Sales Inc Due to...
The Issue: Potential cybersecurity vulnerability that could lead to a Denial of Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOPATH ECHELON 45mm RELOADS WITH GRIPPING SURFACE TECHNOLOGY (GST)...
The Issue: There is the potential for incomplete staple line formation during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eprontia (topiramate) oral solution Recalled by Azurity Pharmaceuticals,...
The Issue: Failed Impurities/Degradation Specifications: Out of specification Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.