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. 986 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
986 in last 12 months

Showing 25021–25040 of 48,595 recalls

Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensor Catheter 18FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensor Catheter 10FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature sensor Foley catheter 18FR Recalled by Degania Silicone, Ltd....

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensor Catheter 8FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Foley Temperature Sensor Catheter 12FR Recalled by Degania Silicone, Ltd....

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Foley Temperature Sensor Catheter 14FR Recalled by Degania Silicone, Ltd....

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2018· Espiner Medical Ltd

Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...

The Issue: Label was incorrect. The label states that the volume of the retrieval bag...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 20, 2018· Gaia Ethnobotanical LLC

Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...

The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...

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

Class I — Serious Health HazardOngoing
Refund