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. 1,816 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,816 in last 12 months

Showing 3016130180 of 48,595 recalls

DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Potassium Chloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: Leakage of unit dose cups that may occur at the seal.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2017· RAYSEARCH LABORATORIES AB

Recalled Item: Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: An error in NVIDIA GPU (Graphics Processing Unit) card drivers can occur for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance 64 System Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance iCT SP X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Argon Medical Devices, Inc

Recalled Item: HARVEST NEEDLE 15GA X 2 Intended for the purpose of Recalled by Argon...

The Issue: The recalling firm received a complaint from one of their customers of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Argon Medical Devices, Inc

Recalled Item: T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN Recalled by Argon Medical...

The Issue: The recalling firm received a complaint from one of their customers of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Argon Medical Devices, Inc

Recalled Item: BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G Recalled by Argon...

The Issue: The recalling firm received a complaint from one of their customers of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance iCT X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity CT X-Ray Recalled by Philips Electronics North...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core128 X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2017· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core X-Ray Recalled by Philips Electronics...

The Issue: During a bolus tracking procedure, no images were generated when the scan...

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

Class II — Potential Health HazardOngoing