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. 947 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
947 in last 12 months

Showing 42201–42220 of 48,770 recalls

Medical DeviceJanuary 13, 2014· Accuray Incorporated

Recalled Item: Accuray CyberKnife Robotic Radiosurgery System Recalled by Accuray...

The Issue: Potential Safety issue with Synchrony Boom Arm Mounting Assembly - one...

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

Class II — Potential Health HazardOngoing
DrugJanuary 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...

The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...

The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...

The Issue: Defective Container; some of the outer laminate foil pouches allowed in air...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 13, 2014· Merck & Co Inc

Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...

The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 13, 2014· HUMAN SCIENCE FOUNDATION

Recalled Item: PRO ArthMax Dietary Supplement tablets Recalled by HUMAN SCIENCE FOUNDATION...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm and Correct Serum Recalled by Dermamedics, L.L.C. Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Complexion Repair Topical Rehydrating Emulsion in 50 ml and...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm & Correct Cream in 2 oz. containers with SKU number DM1020....

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Therametics Complexion Repair Topical Rehydrating Emulsion in 50 ml and...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Baby's Relief Calm and Repair Cream in 2 oz. Recalled by...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm and Correct Cream 2 oz. containers in the Recalled by...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Complexion Repair Topical Rehydrating Emulsion which was...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Post Procedure Cream Recalled by Dermamedics, L.L.C. Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Hospira Inc.

Recalled Item: DOBUTamine Injection Recalled by Hospira Inc. Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: Discolored solution due to a chip in the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2014· Leica Microsystems, Inc.

Recalled Item: Liquid Mouse Monoclonal Antibody CD15 (NCL-L-CD15) Recalled by Leica...

The Issue: Product does not function as intended up to the expiry date on the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2014· Tandem Diabetes Care Inc

Recalled Item: T:slim Insulin Delivery System Insulin Infusion Pump Recalled by Tandem...

The Issue: Specific lots of insulin cartridges that are used with the T:slim Insulin...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2014· Focus Diagnostics Inc

Recalled Item: Simplexa Flu A/B & RSV Direct assay Recalled by Focus Diagnostics Inc Due to...

The Issue: Focus Diagnostics is initiating an urgent safety notice correction for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2014· Smith & Nephew Inc.

Recalled Item: Smith & Nephew RENASYS-AB Abdominal Dressing Kit with Soft Port Recalled by...

The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...

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

Class II — Potential Health HazardOngoing