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. 2,301 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,301 in last 12 months

Showing 4346143480 of 48,770 recalls

Medical DeviceSeptember 18, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 200 Sterilizer (Single Door) Recalled by Advanced Sterilization...

The Issue: Advanced Sterilization Products (ASP) is recalling the STERRAD 200...

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

Class II — Potential Health HazardOngoing
DrugSeptember 17, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: During stability testing an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: During stability testing an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Amgen, Inc.

Recalled Item: Prolia (denosumab) Injection Recalled by Amgen, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible cellulose fibers were observed in a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension LOCI TNI Troponin I Calibrator RC 621. The Recalled by...

The Issue: Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: Aquarius (TM) TEMPERATURE THERAPY Recalled by DeRoyal Industries Inc Due to...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
DrugSeptember 16, 2013· Hospira, Inc.

Recalled Item: 1% Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Oxidized stainless steel found in vial of 1%...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 16, 2013· Hospira, Inc.

Recalled Item: Morphine Sulfate Injection Recalled by Hospira, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Confirmed customer report of leakage of vial...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2013· Osmotica Pharmaceutical Corp

Recalled Item: Venlafaxine (Venlafaxine Hydrochloride) extended release Tablets Recalled by...

The Issue: Failed Dissolution Specification:12 hour time point at 18 months of product...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing