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 2078120800 of 27,850 recalls

Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Del Medical, Inc.

Recalled Item: VS300 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...

The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Teleflex Medical

Recalled Item: Servo Humidifier 163 Recalled by Teleflex Medical Due to Cracks may occur at...

The Issue: Cracks may occur at the 15mm and 22mm ISO female connector.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Smiths Medical ASD Inc.

Recalled Item: Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion Recalled...

The Issue: There have been intermittent issues with Supercap POST (power on self-test)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Gsi Group Inc

Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...

The Issue: The item was recalled due to an increased user/patient risk of exposure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal Standard Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHES Recalled by Synthes (USA) Products LLC Due to The 13.5mm Medullary...

The Issue: The 13.5mm Medullary Reamer head, lot #F-17180, is etched as dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 33 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 21 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 20 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 23 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 34 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Draeger Medical, Inc.

Recalled Item: Optional PS500 Power Supply Unit for the Evita V500 Ventilator Recalled by...

The Issue: The firm became aware of cases in which the battery run times of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing