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 1534115360 of 48,770 recalls

Medical DeviceApril 22, 2021· Remel Inc

Recalled Item: Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin Recalled by Remel Inc...

The Issue: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· Potomac River Group, Corp.

Recalled Item: RAPTAR Laser Range Finders Recalled by Potomac River Group, Corp. Due to...

The Issue: RAPTAR units are capable of being field modified to enable the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· INNOVATIVE TOMOGRAPHY PRODUCT GMBH

Recalled Item: Semi-automatic Biopsy-Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...

The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· INNOVATIVE TOMOGRAPHY PRODUCT GMBH

Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...

The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· INNOVATIVE TOMOGRAPHY PRODUCT GMBH

Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...

The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· Anodyne Surgical

Recalled Item: Hydrodissection Cannula (Chang) Recalled by Anodyne Surgical Due to The...

The Issue: The product may have a yellowish-brown/greenish-brown residue present at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24...

The Issue: Evaluation of a clinical goal for the voxelwise worst dose distributions may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· MICROVENTION INC.

Recalled Item: VIA Microcatheter VIA 21 - Product Usage: is Recalled by MICROVENTION INC....

The Issue: Due to inadvertently shipping to U.S. customers with international labeling...

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

Class III — Low RiskOngoing
Medical DeviceApril 21, 2021· MICROVENTION INC.

Recalled Item: VIA Microcatheter VIA 17 - Product Usage: is Recalled by MICROVENTION INC....

The Issue: Due to inadvertently shipping to U.S. customers with international labeling...

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

Class III — Low RiskOngoing
Medical DeviceApril 21, 2021· MICROVENTION INC.

Recalled Item: VIA Microcatheter VIA 27 - Product Usage: is Recalled by MICROVENTION INC....

The Issue: Due to inadvertently shipping to U.S. customers with international labeling...

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

Class III — Low RiskOngoing
Medical DeviceApril 21, 2021· Dentech Corp.

Recalled Item: Rubber Dam Clamp Recalled by Dentech Corp. Due to Removing parts for safety...

The Issue: Removing parts for safety reasons due to possible breakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· Pentax of America Inc

Recalled Item: Pentax Medical Video Duodenoscope - Product Usage: intended to be Recalled...

The Issue: IFU updated: The warning section of the IFU for both the OE-A63 distal end...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Centaur Syphilis Assay-SYP Kit Recalled by Siemens Healthcare Diagnostics,...

The Issue: Potential for the ADVIA Centaur Syphilis assay to carryover into other...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· Boston Scientific Corporation

Recalled Item: ELUVIA Drug-Eluting Vascular Stent System - Product Usage: indicated for...

The Issue: One batch of the ELUVIATM Drug Eluting Vascular Stent System incorrect...

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

Class II — Potential Health HazardOngoing
DrugApril 20, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Hi-Lite Orange 26 mL Applicator (2% w/v chlorhexidine Recalled...

The Issue: Defective Delivery System: An increase in complaints identified endcap being...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2021· Genentech Inc

Recalled Item: Evrysdi (risdiplam) for oral solution Recalled by Genentech Inc Due to...

The Issue: Defective Container: complaints received regarding some incorrect...

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

Class III — Low RiskOngoing
Refund
FoodApril 20, 2021· Forest Mushroom Food Inc.

Recalled Item: Guan's Enoki Mushroom - Champigons d'enoki Recalled by Forest Mushroom Food...

The Issue: Michigan Department of Agriculture and Rural Development sampled Enoki...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 20, 2021· Medivators, Inc.

Recalled Item: Dialysate Concentrate for Hemodialysis-Liquid/Powd - Product Usage: used in...

The Issue: The lot may have experienced an anomaly during the manufacturing process,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2021· Elekta, Inc.

Recalled Item: Elekta MOSAIC Oncology Information System versions: 2.62 Recalled by Elekta,...

The Issue: Malware attack

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Multitom RAX with software version VF10 Recalled by Siemens Medical...

The Issue: Siemens identified two issues, In some cases, it is possible to perform an...

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

Class II — Potential Health HazardOngoing