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. 1,118 recalls have been distributed to Maine in the last 12 months.
Showing 1561–1580 of 27,655 recalls
Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator 8CM Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...
The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...
The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product: Atellica CH Diluent - CONS 2 x 1.5L Recalled by Siemens Healthcare...
The Issue: Contamination of the diluent by sodium hypochlorite (NaOCl) which may impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemodynamics Software Recalled by CHANGE...
The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen...
The Issue: Due to a software/firmware issue diabetes management system may provide a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport HT70 Ventilator Recalled by Covidien Due to Ventilator Printed...
The Issue: Ventilator Printed Circuit Board Assembly may have two separate capacitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...
The Issue: Due to customer complaints, there is the possibility that catheter needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest...
The Issue: Due to demonstration units of chest compression system being provided to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ColoSense Test Kit Recalled by Geneoscopy, Inc. Due to Multiple plate...
The Issue: Multiple plate failures documented as a result of the Low Positive Template...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.