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. 2,392 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,392 in last 12 months

Showing 2288122900 of 48,770 recalls

Medical DeviceDecember 20, 2018· TERRIFIC CARE LLC

Recalled Item: CoaguChek XS PT Test Recalled by TERRIFIC CARE LLC Due to Potential for...

The Issue: Potential for abnormally high INR test results with the CoaguChek XS PT Test...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2018· Becton Dickinson & Co.

Recalled Item: Phoenix AST Indicator Recalled by Becton Dickinson & Co. Due to Panels...

The Issue: Panels inoculated using certain lots of the indicator solution are...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Centricity Universal Viewer Breast Imaging Centricity...

The Issue: When switching back & forth between multiple UV instances in the Windows...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Becton Dickinson & Co.

Recalled Item: Phoenix AP AST Indicator Bag Recalled by Becton Dickinson & Co. Due to...

The Issue: Panels inoculated using certain lots of the indicator solution are...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Steris Corporation

Recalled Item: AMSCO 5000 Series Washer/Disinfector Model # 5052 Recalled by Steris...

The Issue: The software in the systems may not process the cycle originally intended....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2018· Becton Dickinson & Co.

Recalled Item: Phoenix AST-s Indicator Recalled by Becton Dickinson & Co. Due to Panels...

The Issue: Panels inoculated using certain lots of the indicator solution are...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Associates of Cape Cod, Inc.

Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...

The Issue: The kits may contain the incorrect number of components or the kits may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...

The Issue: Evidence supports that when customers performed a fuse replacement as part...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...

The Issue: A software update is being issued to correct multiple issues identified in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Boston Scientific Corporation

Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...

The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...

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

Class II — Potential Health HazardOngoing
DrugDecember 19, 2018· Teva Pharmaceuticals USA

Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: Mint Chocolate Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: Coconut Chocolate RXBARs Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: KIDS Apple Cinnamon Raisin Recalled by CHICAGO BAR COMPANY LLC RXBAR...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: RXBAR: Pumpkin Spice Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 19, 2018· CHICAGO BAR COMPANY LLC RXBAR

Recalled Item: Chocolate Sea Salt RXBARs Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...

The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...

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

Class II — Potential Health HazardOngoing
Refund