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. 2,492 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,492 in last 12 months

Showing 1460114620 of 48,770 recalls

Medical DeviceJuly 29, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...

The Issue: There was no label on the pad packaging or notification in the user manual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Beckman Coulter Inc.

Recalled Item: Power Processor 3K Recalled by Beckman Coulter Inc. Due to Missing splash...

The Issue: Missing splash guard which may expose users to hazardous materials. .

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin BIOLOX Delta Mod Head Recalled by Corin Ltd Due to The packaging...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin MetaFix Hip Stem Recalled by Corin Ltd Due to The packaging system on...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee Patella Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity-i Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Liner ECIMA Recalled by Corin Ltd Due to The packaging system...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Dual Mobility Recalled by Corin Ltd Due to The packaging...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Corin Ltd

Recalled Item: Corin Trinity Screw Recalled by Corin Ltd Due to The packaging system on the...

The Issue: The packaging system on the devices have potential physical and water damage...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek SmartView Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2021· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Test strip vials may open while inside sealed cartons during shipment. An...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: GoodSense Aller.Ease Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: CVS Allergy Relief Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Meijer allergy relief Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Perrigo Fexofenadine Hydrochloride tablets Recalled by Perrigo Company PLC...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund