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. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 2858128600 of 48,770 recalls

Medical DeviceMay 15, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...

The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Perkinelmer Life Sciences, Inc.

Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...

The Issue: Potential for electric shock in the case of a failure to install the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Beckman Coulter Inc

Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...

The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...

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

Class II — Potential Health HazardOngoing
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Ball in Polybag 24/12oz. Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Cake in Polybag 10/2.2lbs Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Tofu in Polybag 40/240g Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Cake in Polybag 10/930g Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 15, 2017· Wang Globalnet

Recalled Item: Fish Cake in Polybag 20/1lb. Recalled by Wang Globalnet Due to Undeclared Egg

The Issue: Fish products contain undeclared egg and wheat.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 12, 2017· Mesa Laboratories, Inc.

Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....

The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Argon Medical Devices, Inc

Recalled Item: Clear Flashback Needle 7cm x 18G AMC/4 Recalled by Argon Medical Devices,...

The Issue: Argon Medical has received a complaint from one of their distributors of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Teleflex Medical

Recalled Item: Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets...

The Issue: Product size listed on the labeling is incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Brivo MR355 Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Signa PET/MR (K163619 Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Philips Electronics North America Corporation

Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...

The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Discovery MR750 3.0T Product Usage: Intended use: The Discovery MR750...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: SIGNA Creator Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDxt Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing