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. 2,529 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,529 in last 12 months

Showing 68216840 of 27,655 recalls

Medical DeviceJanuary 16, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: SIEMENS Biograph mCT: a) Flow 64-4R Seismic Recalled by Siemens Medical...

The Issue: This is a potential problem with the locking mechanism that is used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: SIEMENS Biograph Vision: a) 450 Recalled by Siemens Medical Solutions USA,...

The Issue: This is a potential problem with the locking mechanism that is used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: SIEMENS Biograph Horizon 3R Mobile Recalled by Siemens Medical Solutions...

The Issue: This is a potential problem with the locking mechanism that is used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2023· Summit Medical, LLC

Recalled Item: Summit Medical Nasal Septal Button Recalled by Summit Medical, LLC Due to...

The Issue: Sterile product pouches were not sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 140 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit- For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2023· S & MOHR AMERICA, S.A. DE C.V.

Recalled Item: abm Respiratory Care Standart Breating Circuit with Face Mask - Recalled by...

The Issue: Incorrect expiration date on product label. The manufacturing date was...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 4, 2023· Wishbone Medical, Inc.

Recalled Item: WishBone Medical Smart Correction Dual Joint Express Struts Recalled by...

The Issue: Firm identified that user may be unable to adjust the length of the Smart...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2023· Bard Peripheral Vascular Inc

Recalled Item: Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter...

The Issue: Due to the adhesive provided within the catheter repair kits maybe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2023· Western/Scott Fetzer Company

Recalled Item: Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR Recalled by...

The Issue: Gauge malfunction: Digital gauge displays an incorrect tank pressure -...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Sterile Hand Pack Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Sterile Oncology Port Access Tray Recalled by MEDLINE INDUSTRIES, LP...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Sterile Maximum Barrier Pack-LF Recalled by MEDLINE INDUSTRIES,...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Incisive CT Recalled by Philips Healthcare (Suzhou) Co., Ltd. Due to...

The Issue: Multiple software issues which have the potential to lead to misdiagnosis...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8 Recalled by...

The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8 Recalled by...

The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...

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

Class II — Potential Health HazardOngoing