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. 2,371 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,371 in last 12 months

Showing 2536125380 of 48,770 recalls

DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Expectorant Cough Syrup Recalled by MBi Distributing Inc. dba MBi...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2018· MBi Distributing Inc. dba MBi Nutraceuticals

Recalled Item: Silver-Zinc Throat Spray Recalled by MBi Distributing Inc. dba MBi...

The Issue: Lack of Processing Controls: Firm is voluntarily recalling all lots of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 15, 2018· Draeger Medical Systems, Inc.

Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...

The Issue: Users have misinterpreted the display for out of range measurement indicated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 15, 2018· Draeger Medical Systems, Inc.

Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...

The Issue: Users have misinterpreted the display for out of range measurement indicated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2018· Beaver Visitec

Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...

The Issue: Blades are loose in handles and may fall out due to non cured epoxy

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2018· Opgen Inc

Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...

The Issue: Possible diminished performance prior to its established expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2018· Merck Millipore Ltd.

Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...

The Issue: In vitro diagnostic devices, used greater than 6 months after date of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...

The Issue: Issuance of validated, new reprocessing procedures. This corrective action...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...

The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...

The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...

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

Class II — Potential Health HazardOngoing
DrugMay 11, 2018· L. Perrigo Company

Recalled Item: Scopolamine Transdermal Therapeutic System Recalled by L. Perrigo Company...

The Issue: Defective delivery system

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Lead Adapter for STar" Drive Recalled by FHC, Inc. Due to...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microtargeting" Depth Stop Adapter Recalled by FHC, Inc. Due to The FHC...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Manual) Recalled by FHC, Inc. Due to The...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized) Distributed by Medtronic...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Lead Adapter for microTargeting" Drive Recalled by FHC, Inc....

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Distributed by Medtronic Recalled by FHC, Inc....

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing