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. 2,562 recalls have been distributed to Maine in the last 12 months.
Showing 881–900 of 27,655 recalls
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump"...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7....
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Recalled...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Recalled...
The Issue: Software issue for hq analyzer results in system not visibly applying...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine Pad-Pak Recalled by HeartSine Technologies Ltd Due to Due to...
The Issue: Due to customer complaints, defibrillator pads may contain damage pins that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combined Spinal and Epidural Anesthesia Tray 2 Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Recalled...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7....
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airvo 2 Recalled by Fisher & Paykel Healthcare, Ltd. Due to When...
The Issue: When unintentionally disconnected from power source, humidifier device (used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM...
The Issue: Firm has received complaints regarding Anti- Valve (ARV) breakage due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P10 series with software version R4.5.7 Model Number 5877534 Recalled...
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Set Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.