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. 2,265 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,265 in last 12 months

Showing 27412760 of 27,655 recalls

Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) ORTHO LAMINECTOMY-LF Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 2) ABDOMINAL LAPAROSCOPY Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· Shimadzu Corp. Analytical & Measuring Instruments Div.

Recalled Item: Autosampler Recalled by Shimadzu Corp. Analytical & Measuring Instruments...

The Issue: There have been cases of failure of the main board due to condensation water...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: SECURE 1000 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix...

The Issue: A limited number of IV bags have been found to leak during filling.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: Imed Products Imed EVA BAG Recalled by The Metrix Company Due to A limited...

The Issue: A limited number of IV bags have been found to leak during filling.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) BASIC NEURO PACK Recalled by MEDLINE...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: Imed Products Imed EVA BAG Recalled by The Metrix Company Due to A limited...

The Issue: A limited number of IV bags have been found to leak during filling.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) CIRCUMCISION PACK Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) GYN LAPAROSCOPY-LF Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: SECURE 50 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix Company...

The Issue: A limited number of IV bags have been found to leak during filling.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· Shimadzu Corp. Analytical & Measuring Instruments Div.

Recalled Item: Autosampler Recalled by Shimadzu Corp. Analytical & Measuring Instruments...

The Issue: There have been cases of failure of the main board due to condensation water...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: CORMIX 150 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix...

The Issue: A limited number of IV bags have been found to leak during filling.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: VYGON 100 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix Company...

The Issue: A limited number of IV bags have been found to leak during filling.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2024· Cook Incorporated

Recalled Item: Approach CTO Micro Wire Guide Recalled by Cook Incorporated Due to Affected...

The Issue: Affected device lots have labels that state the incorrect expiration dates.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2024· Cook Incorporated

Recalled Item: Approach Hydro ST Micro Wire Guide Recalled by Cook Incorporated Due to...

The Issue: Affected device lots have labels that state the incorrect expiration dates.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo. Model Numbers: DS2110X11B Recalled by Philips Respironics, Inc....

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2. Model Numbers: FP2100X10 Recalled by Philips Respironics,...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Potential for the Mains Control Unit board fuse may blow out during system...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing