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. 2,279 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,279 in last 12 months

Showing 4380143820 of 48,770 recalls

FoodAugust 16, 2013· Justin'S Nut Butter

Recalled Item: Chocolate Hazelnut Butter 16oz Jar (Unit Recalled by Justin'S Nut Butter Due...

The Issue: Justin's has initiated a voluntary recall of certain lots of its Maple...

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

Class III — Low RiskOngoing
Refund
FoodAugust 16, 2013· Justin'S Nut Butter

Recalled Item: Maple Almond Butter 16 oz Jar (Unit USPC 894455000322 Recalled by Justin'S...

The Issue: Justi's has initiated a voluntary recall of certain lots of its Maple Almond...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 16, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia S Recalled by Siemens Medical Solutions USA, Inc. Due to The...

The Issue: The detectors on the Symbia S and Symbia T camera systems are supported and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia T Series SPECT + CT Product Usage 1) SPECT: Recalled by Siemens...

The Issue: The detectors on the Symbia S and Symbia T camera systems are supported and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Intact PTH Calibrator (6 pack) Recalled by Siemens Healthcare...

The Issue: PTH Calibrator packaged with only high calibrator.

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

Class III — Low RiskOngoing
Medical DeviceAugust 16, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT Diagnostic imaging system for fixed or mobile Recalled...

The Issue: Issues with the Ingenuity TF PET/CT Software Version 4.0 could pose a risk...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· GE Healthcare, LLC

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

The Issue: GE Healthcare has become aware of a potential safety issue involving missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2013· Steris Corporation

Recalled Item: Harmony Equipment Management System Recalled by Steris Corporation Due to...

The Issue: Dr¿ger Medical GmbH has notified STERIS of the potential for a break in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2013· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...

The Issue: The manufacturer has conducted a review of the results of product testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2013· Elekta, Inc.

Recalled Item: DMLC IV-ERGO - Beam shaping block for Radiation Therapy. Recalled by Elekta,...

The Issue: Clinical mistreatment may occur when there are errors in the clinical...

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

Class II — Potential Health HazardOngoing
DrugAugust 14, 2013· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible particulate embedded in the glass...

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

Class II — Potential Health HazardOngoing
Refund