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. 2,641 recalls have been distributed to Arkansas in the last 12 months.
Showing 5201–5220 of 28,355 recalls
Recalled Item: Medline Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Medline...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline Industries, LP is recalling certain kits and trays that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian 4 Glucose Sensor Recalled by Medtronic MiniMed, Inc. Due to Some...
The Issue: Some sensors may have a glucose oxidase (GOX) layer thickness outside of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoClean 2 Recalled by SoClean, Inc Due to New User Manual with additional...
The Issue: New User Manual with additional instructions for use and a hose and mask...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoClean 3 Recalled by SoClean, Inc Due to New User Manual with additional...
The Issue: New User Manual with additional instructions for use and a hose and mask...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set Recalled by...
The Issue: There is to an increase in complaints related to failure alarms for Wet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to BD (C.R. Bard)...
The Issue: BD (C.R. Bard) has received user complaints reporting that when the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX Spectranetics...
The Issue: Incorrect product labeling. Exterior product box label does not match...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Recanalization System Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Recanalization systems may be in a manufacturing mode that allows the system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide...
The Issue: CARDIOHELP-i System was not properly tested to measure leakage current
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibration Serum Level 3. CAL 3 Recalled by Randox Laboratories Ltd. Due to...
The Issue: There have been transcription errors on the Instructions For Use (IFU) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORI REAL INTELLIGENCE Robotic Drill Recalled by Blue Belt Technologies, Inc...
The Issue: Possibility that the user is unable to resolve drill disconnection error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS...
The Issue: Identification label on affected hookups could become illegible over time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous probe connection cable ( and 701048804) used with Recalled by Maquet...
The Issue: Firm received complaints of breaks in the insulation, shielding, or wires of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for endoscopic dilation...
The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.