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. 2,366 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,366 in last 12 months

Showing 2642126440 of 48,770 recalls

Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STRL Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 11X180 125DG STRL Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ACE TROCH NAIL 125 DEG. X Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER L H TROC NAIL 320X9X125 Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC LAG SCR 70 MM Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X11X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Boston Scientific Corporation

Recalled Item: SpyScope DS Access and Delivery diagnostic biliary catheter Recalled by...

The Issue: Certain lots of devices may have the working channel sleeve protruding from...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: ultraView SISH DNP Detection Kit Recalled by Ventana Medical Systems Inc Due...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Cook Inc.

Recalled Item: Echosight Jansen-Anderson Intratubal Transfer Set Recalled by Cook Inc. Due...

The Issue: Certain lots of in vitro fertilization (IVF) products were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: Hematoxylin II Recalled by Ventana Medical Systems Inc Due to Increased...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: CINtec PLUS Cytology Kit (CE-IVD) Recalled by Ventana Medical Systems Inc...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: ultraView SISH DNP Detection Kit US Recalled by Ventana Medical Systems Inc...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing