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. 2,553 recalls have been distributed to Arkansas in the last 12 months.
Showing 15821–15840 of 28,355 recalls
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Express Fluid Warmer (FW-300 Recalled by NxStage Medical, Inc. Due...
The Issue: There is a potential risk of electrical fire when fluid leaks into the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nokia BPM+ Wireless Blood Pressure Monitor Product System Recalled by...
The Issue: Device could not meet the requirements for systolic pressure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Chamber Temporary External Pacemaker Recalled by Medtronic Inc.,...
The Issue: A subset of Medtronic Model 53401 Single Chamber External Pulse Generators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the...
The Issue: GE Medical Systems has discovered a small area on the bore surface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.