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. 2,623 recalls have been distributed to Arkansas in the last 12 months.
Showing 8341–8360 of 28,355 recalls
Recalled Item: Coryell Memorial Hosp Total Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicare Neuro Pack - Neurological Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Pack - Surgical Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lum Lam Custom Pack - Anesthesia Kit Recalled by Stradis Medical, LLC dba...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S Recalled by...
The Issue: Devices distributed lacked regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software model numbers: 20910-01 Recalled by Brainlab AG...
The Issue: The yaw angle may be incorrect for CBCT positioning workflows using setup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer Packaging Label: Protekt Sharps Safety Knives - 44620MU Recalled by...
The Issue: Surgical knives may contain incorrect description printed on handles....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceOAR Vue System Recalled by Boston Scientific Corporation Due to Users...
The Issue: Users need to be aware that embolism is a possible adverse event associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...
The Issue: Users need to be aware that embolism is a possible adverse event associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Custom Procedure Kits containing BD Luer Lok Access Devices Recalled...
The Issue: Recalled devices were packaged in convenience kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If the...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q zeego Recalled by Siemens Medical Solutions USA, Inc Due to If the...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee multi-purpose Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.