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. 2,491 recalls have been distributed to Arkansas in the last 12 months.
Showing 20201–20220 of 28,355 recalls
Recalled Item: Various trauma and sports medicine instruments and implants. Passer....
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart CR Digital Computed Radiography System Recalled by Fujifilm Medical...
The Issue: Reports of failure of the device's power supply.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Pin Recalled by...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Arthroscope....
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Fastener...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. cannula...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Appliance...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Spinal...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core-Computed Tomography X-ray system Product Usage: The Ingenuity...
The Issue: Philips Healthcare received reports from the field that certain Ingenuity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Bit Recalled by...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Direct Drive Clip Applier CA090 Recalled by Applied Medical Resources Corp...
The Issue: Increased customer complaints indicating inconsistent clip application; may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Recalled by B...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Orthopedic...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. guide Recalled...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Philips Healthcare received reports from the field that certain Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Rod Recalled by...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128-Computed Tomography X-ray system Product Usage: The...
The Issue: Philips Healthcare received reports from the field that certain Ingenuity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various trauma and sports medicine instruments and implants. Screw Recalled...
The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code...
The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.