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. 2,329 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,329 in last 12 months

Showing 3780137820 of 48,770 recalls

FoodMarch 15, 2015· Gourmet Kitchen, Inc.

Recalled Item: Spicy Shrimp Chopsticks 80 PCS S5038 15075 Products are placed Recalled by...

The Issue: Products may contain peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 15, 2015· Gourmet Kitchen, Inc.

Recalled Item: Lobster & Shrimp Spring Rolls Products are placed on plastic trays Recalled...

The Issue: Products may contain peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 15, 2015· Gourmet Kitchen, Inc.

Recalled Item: Appetizer Size Lobster Spring Rolls 80 PCS L1046 15075 Products Recalled by...

The Issue: Products may contain peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 13, 2015· ProThera, Inc.

Recalled Item: Klaire Labs Ther-Biotic FACTOR 6 100+ Billion CFU's Multi-Species Probiotic...

The Issue: Firm is recalling three lots of Ther-Biotic dietary supplements due to...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 13, 2015· ProThera, Inc.

Recalled Item: Klaire Labs Ther-Biotic Children's Chewable 125+ Billion CFU's Multi-Species...

The Issue: Firm is recalling three lots of Ther-Biotic dietary supplements due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 13, 2015· Vital Signs Colorado Inc.

Recalled Item: Introduction Pack. A device inserted into an endotracheal tube to Recalled...

The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Nuclear Gamma Cameras (ADAC Vertex Classic Recalled by Philips Medical...

The Issue: During clinical use of a Vertex Plus Gamma Camera, as the detector heads...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2015· Vital Signs Colorado Inc.

Recalled Item: CareFusion Vital Signs LightWand Stylet. A device inserted into an Recalled...

The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Polaris 4.75 TI Spinal System Recalled by Biomet Spine, LLC Due to...

The Issue: Multiaxial screws may not meet internal requirements related to fatigue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network Recalled by Mindray DS USA, Inc. dba...

The Issue: Software anomaly in the Panorama System software version 8.9 that manifests...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Lineum HF Torque Handle Limit (Lineum) Model Number 14-525035 P_roduct...

The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· GE Healthcare

Recalled Item: GE Healthcare Recalled by GE Healthcare Due to GE Healthcare has recently...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· CareFusion 303, Inc.

Recalled Item: Alaris PC units Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the Alaris PC unit because of an error code. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2015· Biomet Spine, LLC

Recalled Item: Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage:...

The Issue: Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque...

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

Class II — Potential Health HazardOngoing
FoodMarch 12, 2015· Trader Joes Company

Recalled Item: Cinnamon Almonds Recalled by Trader Joes Company Due to Undeclared Peanuts

The Issue: Trader Joes Company is recalling its 16 ounce packages of Trader Joes...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 12, 2015· Wockhardt Usa Inc.

Recalled Item: Captopril Tablets Recalled by Wockhardt Usa Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: out of specification for thickness.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2015· Hospira Inc.

Recalled Item: LACTATED RINGER'S IRRIGATION Recalled by Hospira Inc. Due to Non-Sterility:...

The Issue: Non-Sterility: Confirmed customer report of dark, fibrous particulates...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 11, 2015· Toshiba American Medical Systems Inc

Recalled Item: INFX-8000V Interventional Angiography System. CAT-880B catheterization...

The Issue: The table base rotational brake that holds the table top may not always be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Nuclear gamma cameras (ADAC VERTEX PLUS/SOLUS/CARDIO Recalled by Philips...

The Issue: The firm was notified by a customer that the collimator exchange carriage...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2015· Mylan Pharmaceuticals Inc.

Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund