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. 2,518 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,518 in last 12 months

Showing 1096110980 of 48,770 recalls

DrugAugust 26, 2022· Carolina Infusion

Recalled Item: TEST CYP/PROP (50:50) 100 MG/100 MG/ML Injectable Recalled by Carolina...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: Semaglutide/Cyanocobalamin 10/2 MG/ML Injectable Recalled by Carolina...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: L-Carnitine 500 mg/mL Injectable Recalled by Carolina Infusion 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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: TRI-MIX 30/2/20 Injectable Recalled by Carolina Infusion Due to Lack of...

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
DrugAugust 26, 2022· Carolina Infusion

Recalled Item: QUAD-MIX 30MG/3MG/60MCG/0.2 Injectable Recalled by Carolina Infusion Due to...

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 DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP A30 Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP V30 Auto Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced+ Intl (Flow Gen) Recalled by Philips Respironics,...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced + with Heated Tube Humidifier Recalled by Philips...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP A40 Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced+ Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2022· Zimmer, Inc.

Recalled Item: G7 Acetabular System Recalled by Zimmer, Inc. Due to The outer sterile...

The Issue: The outer sterile package cavity has a corner wall thickness that is below...

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

Class II — Potential Health HazardOngoing
FoodAugust 24, 2022· D. F. Stauffer Biscuit Co, Inc.

Recalled Item: White frosted animal cookies with multi-colored non-pareils in a 44oz...

The Issue: Potential contamination with foreign material (metal).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 24, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent...

The Issue: Dimension Vista¿ High Density Lipoprotein Cholesterol (HDLC) Potential for...

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

Class II — Potential Health HazardOngoing
DrugAugust 23, 2022· Leading Pharma, LLC

Recalled Item: ClomiPRAMINE Hydrochloride Capsules Recalled by Leading Pharma, LLC Due to...

The Issue: Superpotent Drug: Assay value found to be 110.6% in Chlomipramine...

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

Class III — Low RiskOngoing
Refund
DrugAugust 23, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Neomycin Sulfate Tablets Recalled by Teva Pharmaceuticals USA Inc Due to...

The Issue: CGMP Deviations: A foreign matter identified as teflon was found in the...

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

Class II — Potential Health HazardOngoing
Refund