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 2490124920 of 48,770 recalls

Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Cesar Powerpack-Visub(V3000) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 Biplane DR Table Recalled by Philips Electronics North...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Cesar-DMCP-Visub(HM2000/3000) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AlluraXperFOlO/lO Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (biplane) Recalled by Philips Electronics North...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 F FDXD Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AIIuraXperFDlO Recalled by Philips Electronics North America Corporation Due...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD2O Biplane Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F010 Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: RAPIDLab 1265 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics,...

The Issue: Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: RAPIDLab 1245 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics,...

The Issue: Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: RAPIDPoint 500 Blood Gas Analyzer Recalled by Siemens Healthcare...

The Issue: Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: RAPIDPoint 405 Blood Gas Analyzer Recalled by Siemens Healthcare...

The Issue: Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· In2bones USA, LLC

Recalled Item: CoLink(TM) Lapidus Plate XP Recalled by In2bones USA, LLC Due to CoLink(TM)...

The Issue: CoLink(TM) Lapidus Plate +2mm Right and Left, were laser marked incorrectly....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· In2bones USA, LLC

Recalled Item: CoLink(TM) Lapidus Plate XP Recalled by In2bones USA, LLC Due to CoLink(TM)...

The Issue: CoLink(TM) Lapidus Plate +2mm Right and Left, were laser marked incorrectly....

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

Class II — Potential Health HazardOngoing
FoodJuly 14, 2018· Utz Quality Food Inc

Recalled Item: utz Carolina Style Barbeque Potato Chips Recalled by Utz Quality Food Inc...

The Issue: Utz¿ Quality Foods, LLC., is voluntarily recalling select expiration dates...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 13, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer - 723G8 Product Usage - In Recalled by Tosoh...

The Issue: Analyzers were distributed with software which lacks a 510K

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T HEMODIALYSIS SYSTEM W/BIBAG Recalled by Fresenius Medical Care Renal...

The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: 2008T HEMODIALYSIS SYS Recalled by Fresenius Medical Care Renal Therapies...

The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...

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

Class II — Potential Health HazardOngoing