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. 2,492 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,492 in last 12 months

Showing 1482114840 of 48,770 recalls

Medical DeviceJuly 1, 2021· Gibson Bioscience

Recalled Item: Potassium Hydroxide 10% (KOH 10%) Recalled by Gibson Bioscience Due to A lot...

The Issue: A lot of KOH 10% was made with Hydrogen Peroxide 3% instead of KOH 10%.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Howmedica Osteonics Corp.

Recalled Item: Triathlon Prim CEM FXD BPLT 7 Recalled by Howmedica Osteonics Corp. Due to...

The Issue: The internal profile of the Triathlon Prim (Baseplate) is potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Medline Industries Inc

Recalled Item: Medline Arthroscopy Kit Recalled by Medline Industries Inc Due to The kits...

The Issue: The kits may contain an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 ANTIGEN QC Recalled by Beckman Coulter Inc. Due to...

The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 ANTIGEN EXTRACTION SOLUTION Recalled by Beckman Coulter...

The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Medline Industries Inc

Recalled Item: Medline Knee Arthroscopy Kit Recalled by Medline Industries Inc Due to The...

The Issue: The kits may contain an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 Antigen Recalled by Beckman Coulter Inc. Due to SARS-CoV-2...

The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Medline Industries Inc

Recalled Item: Medline Total Knee Recalled by Medline Industries Inc Due to The kits may...

The Issue: The kits may contain an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Medline Industries Inc

Recalled Item: Medline Shoulder CDS convenience kits Recalled by Medline Industries Inc Due...

The Issue: The kits may contain an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Beckman Coulter Inc.

Recalled Item: Access SARS-CoV-2 Antigen Calibrators Recalled by Beckman Coulter Inc. Due...

The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Verathon, Inc.

Recalled Item: GlideScope Go Monitors Recalled by Verathon, Inc. Due to Handheld video...

The Issue: Handheld video monitor failed to meet the labeled IP67 rating which may...

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

Class III — Low RiskOngoing
DrugJune 30, 2021· Cascade Kelly Holdings LLC

Recalled Item: Global Hand Sanitizer with moisturizer Recalled by Cascade Kelly Holdings...

The Issue: CGMP Deviations: Does not meet monograph for denaturant.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2021· Cascade Kelly Holdings LLC

Recalled Item: Global Hand Sanitizer with moisturizer Recalled by Cascade Kelly Holdings...

The Issue: CGMP Deviations: Does not meet monograph for denaturant.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 30, 2021· GE Healthcare, LLC

Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to The accumulated dose...

The Issue: The accumulated dose is incorrectly displayed in certain situations. There...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· GE Healthcare, LLC

Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to The accumulated dose is...

The Issue: The accumulated dose is incorrectly displayed in certain situations. There...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· GE Healthcare, LLC

Recalled Item: Computed Tomography Systems Revolution CT Recalled by GE Healthcare, LLC Due...

The Issue: The accumulated dose is incorrectly displayed in certain situations....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Models with SW version VD12 listed below: Artis zee Recalled by...

The Issue: Due to a software error, the IAS (Image Acquisition System) may sporadically...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: Model L43K Intraoperative Probe-For the diagnostic ultrasound evaluation...

The Issue: The screw cover at the tip of the probe may fall off after a cleaning and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· Olympus Corporation of the Americas

Recalled Item: Soltive Premium Super Pulsed Laser System (TFL-PLS) & Pro Super Recalled by...

The Issue: Thermal injury following dusting and fragmenting treatment of ureteral...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· Merit Medical Systems, Inc.

Recalled Item: Prelude SNAP Splittable Sheath Introducer Recalled by Merit Medical Systems,...

The Issue: There is a potential that 7F sheaths are packaged as 10F sheaths.

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

Class II — Potential Health HazardOngoing