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. 2,524 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,524 in last 12 months

Showing 86218640 of 48,770 recalls

Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: Revize Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: Revize-X Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend MP Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 4.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Meshed Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 2.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: TissueMend Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend PRS Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
DrugMay 22, 2023· New England Life Care, Inc. dba Advanced Compounding Solutions

Recalled Item: Phenylephrine HCl 20 mg added to 0.9% Sodium Chloride 250mL Bag Recalled by...

The Issue: Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250...

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

Class III — Low RiskOngoing
Refund
DrugMay 22, 2023· Aurobindo Pharma USA Inc.

Recalled Item: Pain Reliever Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: firm's investigation due to...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2023· Van Leeuwen Ice Cream LLC

Recalled Item: Van Leeuwen brand BROWN SUGAR CHUNK WITH COOKIE DOUGH & BROWNIES FENCH ICE...

The Issue: Product may contain undeclared walnuts.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 22, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis CII Safe Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing cabinet devices plugged into any multi-socket outlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-10 Recalled by...

The Issue: There are potential risks of the Hemospray powder adhering to the distal end...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2023· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-7 Recalled by...

The Issue: There are potential risks of the Hemospray powder adhering to the distal end...

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

Class II — Potential Health HazardOngoing
DrugMay 19, 2023· Sagent Pharmaceuticals Inc

Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2023· Sagent Pharmaceuticals Inc

Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2023· Sagent Pharmaceuticals Inc

Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 19, 2023· Olympus Corporation of the Americas

Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...

The Issue: Dilator tips may break in the package and in patients during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2023· Qiagen GmbH

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitative test intended...

The Issue: Identified a decreased performance reliability rate, Run abortions could...

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

Class II — Potential Health HazardOngoing