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. 1,872 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,872 in last 12 months

Showing 1984119860 of 27,850 recalls

Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Haskal Transjugular Intrahepatic Portal Access Set Introducer Recalled by...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Lower Back Garment Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V4 Recalled by Carestream Health Inc Due to...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Kumpe Access Catheter Cathether Recalled by Cook Inc. Due to Increase in...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: TM LPS TIB SZ 3 C/D Recalled by Zimmer Trabecular Metal Technology, Inc. Due...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Torcon NB Advantage Catheter Catheter Recalled by Cook Inc. Due...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: FluoroSet Radiographic Tubal Assessment Set Cannula Recalled by Cook Inc....

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter Catheter Recalled by Cook...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Aprima Access Nonvascular Introducer Set Accessories Recalled by Cook Inc....

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Cook Inc.

Recalled Item: Neff DAgostino Percutaneous Access Set Accessories Recalled by Cook Inc. Due...

The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Covidien LLC

Recalled Item: Given Imaging Bravo¿¿ pH capsule delivery device Recalled by Covidien LLC...

The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing