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. 2,371 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,371 in last 12 months

Showing 2504125060 of 48,770 recalls

DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Red Maeng Da Recalled by World Organix, LLC Due to...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Recalled by World Organix, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Kratom+CBD CBD infused Maeng Da Recalled by World Organix,...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Gold Series Ultra Enhanced Indo Recalled by World Organix,...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· MAJOR PHARMACEUTICALS

Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2018· MAJOR PHARMACEUTICALS

Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 26, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood parameter monitoring system 500 H/SAT Recalled by Terumo...

The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Monitor with one Blood Parameter Module and one HSat Probe Recalled by...

The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2018· DJO, LLC

Recalled Item: This is an accessory to Intelect Advanced Recalled by DJO, LLC Due to The...

The Issue: The device accessories were not labeled with appropriate latex warning.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT CLEARVUE isp Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: Certain NAUTILUS DELTA Port Kit product code / lot number combinations may...

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

Class II — Potential Health HazardOngoing
DrugJune 22, 2018· Akorn, Inc.

Recalled Item: Acetylcysteine for Injection 6 g/30 mL (200 mg/mL). Rx Only. Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 22, 2018· Talking Rain Beverage Co Inc

Recalled Item: Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water Recalled by...

The Issue: Sparkling ICE Cherry Limeade, 17 oz. bottles, is recalled after the firm...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 22, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...

The Issue: Potential hardware issue which may cause thermal effects and possible damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...

The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial...

The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...

The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2018· Clarity Diagnostics Llc

Recalled Item: Clarity Urocheck 10SG Urinalysis Strips Recalled by Clarity Diagnostics Llc...

The Issue: Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are...

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

Class III — Low RiskOngoing
Medical DeviceJune 22, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q. angiography system. Model 10848280 Recalled by Siemens Medical...

The Issue: Potential hardware issue which may cause thermal effects and possible damage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The flow rate test verification was not properly executed for certain Sigma...

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

Class II — Potential Health HazardOngoing