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.
Showing 14521–14540 of 48,770 recalls
Recalled Item: Vysis CLL FISH Probe Kit with the following components: Vysis Recalled by...
The Issue: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System...
The Issue: Customers have reported an increased number of false positive SARS-CoV-2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Gel labeled under the following brand names: MediChoice...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...
The Issue: Potential for the plunger to draw back after the air has been expelled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by The Harvard Drug Group Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution Recalled by Teligent Pharma, Inc....
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AquaBplus Water Purification System Recalled by Fresenius Medical Care...
The Issue: AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...
The Issue: There is potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8 Recalled by...
The Issue: Packaging seal defect may allow a breach of the package sterile barrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 365 SKINNY High Intensity Capsules Recalled by Je Dois Lavoir LLC Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artificial Tears Ointment Recalled by Akorn, Inc. Due to Non-Sterility - OOS...
The Issue: Non-Sterility - OOS sterility testing observed during 12-month controlled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clopidogrel Tablets Recalled by Macleods Pharma Usa Inc Due to Presence of...
The Issue: Presence of foreign matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: uEXPLORER PET/CT System - Product Usage: intended to be operated Recalled by...
The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow sensors that may be installed in the following GEHC Recalled by GE...
The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uMI 550 System - Product Usage: intended to be operated Recalled by Shanghai...
The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow sensors kept as stand-alone user replaceable spare parts for Recalled...
The Issue: The flow sensors built prior to June 2021 could have damaged tubes with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite Recalled by CAREFUSION Due...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free...
The Issue: Needle-free connector valves, either standalone or attached to extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.