Product Recalls in New Mexico

Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,839 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,839 in last 12 months

Showing 2606126080 of 48,595 recalls

DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Tramadol HCl USP (CIV) for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Liothyronine Sodium USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Oxandrolone USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Estradiol Hemihydrate USP (Micronized) (Soy) for prescription compounding...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Nandrolone Decanoate USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Prilocaine HCl USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Diclofenac Sodium USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2018· Divinity Product Distribution LLC

Recalled Item: Kratom powder labeled in the following ways 1) Enhance Your Life Recalled by...

The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2018· Divinity Product Distribution LLC

Recalled Item: Kratom capsules labeled in the following ways: 1) Divinity Kratom Recalled...

The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT(R) ClearVUE(R) isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing