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. 2,379 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,379 in last 12 months

Showing 2144121460 of 27,655 recalls

Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Fios First Entry Recalled by Stryker Sustainability Solutions Due to Stryker...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Cannula and Seal Recalled by Stryker Sustainability Solutions Due to Stryker...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Elekta, Inc.

Recalled Item: Laksell GammaPlan Recalled by Elekta, Inc. Due to Memory can become...

The Issue: Memory can become corrupted when creating a fused study via drag and drop in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2015· Merge Healthcare, Inc.

Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...

The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova 2100IQ. Angiographic X-ray systems used in generating...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Triathlon PS X3 Tibial Insert Recalled by Stryker Howmedica Osteonics Corp....

The Issue: Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Tecan US, Inc.

Recalled Item: Infinite F500 Recalled by Tecan US, Inc. Due to A firmware bug causes...

The Issue: A firmware bug causes incorrect values to be displayed for specific measured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova IGS 530. Angiographic X-ray systems used in Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Tecan US, Inc.

Recalled Item: Infinite 200 in vitro diagnostic. Product Usage: The Tecan Infinite Recalled...

The Issue: A firmware bug causes incorrect values to be displayed for specific measured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova 3100IQ. Angiographic X-ray systems used in generating...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Optima IGS 320. Angiographic X-ray systems used in Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· Tecan US, Inc.

Recalled Item: Infinite 200 PRO in vitro diagnostic. Product Usage: The Tecan Recalled by...

The Issue: A firmware bug causes incorrect values to be displayed for specific measured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova IGS 630. Angiographic X-ray systems used in Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2015· GE Healthcare

Recalled Item: GE Healthcare Innova IGS 620. Angiographic X-ray systems used in Recalled by...

The Issue: GE Healthcare has recently become aware of a potential safety issue that may...

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

Class II — Potential Health HazardOngoing