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. 2,352 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,352 in last 12 months

Showing 3396133980 of 48,770 recalls

Medical DeviceFebruary 4, 2016· Draeger Medical, Inc.

Recalled Item: Evita Infinity V500 Ventilator Recalled by Draeger Medical, Inc. Due to The...

The Issue: The battery capacity of the optional PS500 power supply unit for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2016· Medical Action Industries Inc

Recalled Item: PICC/CVC Secure Dressing Change kit Recalled by Medical Action Industries...

The Issue: Misbranding; Due to the presence of CHG in the Tegaderm PICC/CVC dressing...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2016· Zimmer Spine, Inc.

Recalled Item: Virage OCT Spinal Fixation System. Intended to promote fusion of Recalled by...

The Issue: Zimmer Biomet Spine is initiating a Medical Device Correction regarding the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2016· Hospira Inc.

Recalled Item: Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Confirmed customer...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2016· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone Diacetate Injectable Suspension Recalled by Isomeric Pharmacy...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: some vials may be...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 2, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed Recalled by Stryker Medical Division of Stryker Corporation...

The Issue: CPU board failures cause fowler (backrest) electronic controls to stop working.

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

Class II — Potential Health HazardOngoing
FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's Premium Teriyaki Marinade Recalled by Geneva Foods, LLC Due to...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's All Natural Spicy Bourbon Flavor Rub Recalled by Geneva Foods,...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's All Natural Bourbon Flavor Rub Recalled by Geneva Foods, LLC Due...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge FlexConnect software Recalled by Merge Healthcare, Inc. Due to...

The Issue: Communication protocols interfacing with the affected software version with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: CADstream software. The firm name on the label is Merge Healthcare Recalled...

The Issue: The software was not presenting the PURE filter user interface message on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is an integrated Recalled...

The Issue: Patient information in the header is only found on the first page of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Access used with Merge PACS software provides medical specialists...

The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Access used with Ortho PACS software provides medical specialists...

The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Product was distributed under the AMICAS label Recalled...

The Issue: The patient name in the Halo title bar and the thumbnails do not match the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...

The Issue: A migrated study that has annotations will display the annotations, but when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...

The Issue: Potential data loss occurs as a result of the software archiving not working...

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

Class II — Potential Health HazardOngoing
FoodJanuary 29, 2016· Garden Of Life Llc

Recalled Item: Raw Meal Organic Vanilla Spiced Chai Powder Recalled by Garden Of Life Llc...

The Issue: Products possibly contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 29, 2016· Garden Of Life Llc

Recalled Item: Raw Meal Organic Vanilla Powder Recalled by Garden Of Life Llc Due to...

The Issue: Products possibly contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 29, 2016· Garden Of Life Llc

Recalled Item: Raw Meal Organic Original Powder Recalled by Garden Of Life Llc Due to...

The Issue: Products possibly contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund