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. 2,301 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,301 in last 12 months

Showing 4312143140 of 48,770 recalls

FoodOctober 22, 2013· Reser's Fine Foods, Inc.

Recalled Item: Tuna Salad Recalled by Reser's Fine Foods, Inc. Due to Potential Listeria...

The Issue: The recalled products are potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2013· Reser's Fine Foods, Inc.

Recalled Item: Reser's American Harvest BBQ Beans Recalled by Reser's Fine Foods, Inc. Due...

The Issue: The recalled products are potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2013· Reser's Fine Foods, Inc.

Recalled Item: Reser's Baked Potato Salad Recalled by Reser's Fine Foods, Inc. Due to...

The Issue: The recalled products are potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2013· Reser's Fine Foods, Inc.

Recalled Item: The Deli Counter Classic Cole Slaw Recalled by Reser's Fine Foods, Inc. Due...

The Issue: The recalled products are potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 22, 2013· Reser's Fine Foods, Inc.

Recalled Item: The Deli Counter Seafood with Shrimp Salad Recalled by Reser's Fine Foods,...

The Issue: The recalled products are potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 21, 2013· Medisca Inc.

Recalled Item: Human Chorionic Gonadotropin Recalled by Medisca Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; Firm states that erroneous...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: SuperDigestZyme (Z22) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: RepairVite (K63) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: GlutenFlam (K-52) Enzyme & Bioflavonoid Dietary Supplement Recalled by Apex...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: LGS-Zyme (Z12) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ProVia¿ CROSSING GUIDEWIRE Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Applied Medical Resources Corp

Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...

The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Urologix, Inc.

Recalled Item: Prostiva RF Therapy Hand Piece Kit Recalled by Urologix, Inc. Due to A Hand...

The Issue: A Hand Piece high deployment force exceeded the maximum specification.

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

Class II — Potential Health HazardOngoing