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. 2,266 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,266 in last 12 months

Showing 4746147480 of 48,770 recalls

FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Organic Mild Salsa Recalled by Pulmuone Wildwood Inc Due to The...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Organic Medium Salsa Recalled by Pulmuone Wildwood Inc Due to The...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Hot Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa Recalled by Pulmuone...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2012· Pulmuone Wildwood Inc

Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa - Canada (containing...

The Issue: The firm recalled due to a potential non-safety quality concern related to a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 12, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a number of potential issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2012· Alere San Diego, Inc.

Recalled Item: Alere Triage TOX Drug Screen 9 Panel Recalled by Alere San Diego, Inc. Due...

The Issue: Alere San Diego is recalling Alere Triage TOX Drug Screen because there is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2012· Aesculap Implant Systems LLC

Recalled Item: Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD Recalled...

The Issue: The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are...

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

Class II — Potential Health HazardOngoing
DrugJuly 11, 2012· Actavis

Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Subpotent; some...

The Issue: Subpotent; some patches may not contain fentanyl gel

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: AirFlow Resuscitator Recalled by Ventlab Corporation Due to Possible volume...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: V*Care Resuscitator Infant Resuscitator Recalled by Ventlab Corporation Due...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Adult Resuscitator Recalled by Ventlab Corporation Due to Possible volume...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Ventlab Rescue Med Infant Resuscitator Recalled by Ventlab Corporation Due...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing