Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,536 recalls have been distributed to Maine in the last 12 months.
Showing 5821–5840 of 27,655 recalls
Recalled Item: Alcon Custom Pak Recalled by Alcon Research, LTD. Due to Reports of patient...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phaco Standalone Tips Recalled by Alcon Research, LTD. Due to Reports of...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT SUV Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESSRAIL Platform (Standard Blade) Part Number SB-1000 Recalled by Maquet...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT-i Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT V Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC Due...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6...
The Issue: Thread form issue of the locking holes in that the locking screws would not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISee Ortho-K Lens Recalled by PARAGON VISION SCIENCES, Inc Due to...
The Issue: Manufactured lenses are not covered by existing FDA approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fargo Ortho-K Lens Recalled by PARAGON VISION SCIENCES, Inc Due to...
The Issue: Manufactured lenses are not covered by existing FDA approval
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift Visual Obturator Recalled by Scholly Fiberoptic Gmbh Due to There is...
The Issue: There is an improperly performed weld between the cone of the sheath lock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellacor System with Micro-Coring Technology-Indicated for use by medical...
The Issue: Potential failure of a bearing adhesive joint that can occur due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.