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. 1,058 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,058 in last 12 months

Showing 11721–11740 of 27,850 recalls

Medical DeviceApril 20, 2020· Suntech Medical, Inc.

Recalled Item: Oscar 2 Recalled by Suntech Medical, Inc. Due to The device display, when...

The Issue: The device display, when activated, can show an incorrect decimal point when...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Cios Spin VA30-mobile X-Ray system Recalled by Siemens Medical...

The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Bovie Medical Corporation

Recalled Item: Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B Recalled by...

The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· ROi CPS LLC

Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....

The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Bovie Medical Corporation

Recalled Item: Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS...

The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Philips North America, LLC

Recalled Item: Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are...

The Issue: Internal Paddles may wear over time and may not be safe or ready for use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: B-Hydroxybutyrate LiquiColor Recalled by Cardinal Health Inc. Due to Three...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: Professional Urine Drug Control Recalled by Cardinal Health Inc. Due to...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: Strep B Carrot Broth One-Step Recalled by Cardinal Health Inc. Due to Three...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Baxter Healthcare Corporation

Recalled Item: Gambro Cartridge Blood Transport System for Hemodialysis Blood Set -...

The Issue: Potential disconnection of tubing set.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: 155308 Knees AGC Knee System PS Molded Tibial Component...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: TMJPM-1510 Microfixation Custom Made Device Recalled by...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: 189260 Vanguard Knee System Recalled by Biomet, Inc. Due to...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Baxter Healthcare Corporation

Recalled Item: Gambro Cartridge Low Volume Blood Transport System for Hemodialysis Blood...

The Issue: Potential disconnection of tubing set.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Hip Products Item Number: 1) 110010462 RingLoc Hip System Recalled by...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Baxter Healthcare Corporation

Recalled Item: Gambro Cartridge Blood Set Prime Line - Product Usage: is Recalled by Baxter...

The Issue: Potential disconnection of tubing set.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: 183622 Vanguard Knee System PS Tibial Bearing Recalled by...

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: 184762 Knees Vanguard Knee System Recalled by Biomet, Inc....

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Image-Intensified Fluoroscopic X-Ray System Recalled by Siemens...

The Issue: The unplugging of the main cable on the monitor trolley from the X10...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Biomet, Inc.

Recalled Item: Knee Products: 154335 Oxford Partial Knee System Recalled by Biomet, Inc....

The Issue: Potential presence of elevated endotoxin levels that exceed the...

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

Class II — Potential Health HazardOngoing