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 15621–15640 of 28,355 recalls
Recalled Item: Allura Xper FD2O Recalled by Philips Electronics North America Corporation...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 15-12 (mono) Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NTEGRIS Allura 9 0 FDXD Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper F010/10 DRTable Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD2O Biplane Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlIura Xper F010 F Recalled by Philips Electronics North America Corporation...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 9 Recalled by Philips Electronics North America Corporation...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper F020 DR Table Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper F010 DR Table Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G8 Automated HPLC Analyzer - 723G8 Product Usage - In Recalled by Tosoh...
The Issue: Analyzers were distributed with software which lacks a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VSV (Vital Signs Viewer) Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin...
The Issue: The product was mislabeled with the incorrect label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HEMODIALYSIS SYSTEM W/BIBAG Recalled by Fresenius Medical Care Renal...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS3 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HEMODIALYSIS SYS Recalled by Fresenius Medical Care Renal Therapies...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.