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

48,595 total recalls
913 in last 12 months

Showing 44921–44940 of 48,595 recalls

Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON 60mm Endoscopic Linear Cutter Reloads Black in Flexible Blister...

The Issue: Ethicon Endo-Surgery is initiating a voluntary worldwide recall for ECHELON...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Artis zeego x-ray Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens issued a customer safety notice about the overlay of system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Life Technologies Corporation

Recalled Item: HSV 2 Primers Recalled by Life Technologies Corporation Due to Firm received...

The Issue: Firm received complaints that HSV-2 primers failed to amplify HSV-2 DNA.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Endologix Inc

Recalled Item: Brand Name: AFX" Introducer System Recalled by Endologix Inc Due to...

The Issue: Endologix, Inc. initiated this voluntary recall of certain lots of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2013· Microgenics Corporation

Recalled Item: Thermo Scientific MAS Bilirubin for Siemens and Dimension Vista Systems...

The Issue: It has been confirmed from in-house testing that Direct Bilirubin (DBIL),...

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

Class II — Potential Health HazardOngoing
DrugMay 13, 2013· Abrams Royal Pharmacy

Recalled Item: Trace Mineral-5 MDV Recalled by Abrams Royal Pharmacy Due to Non-Sterility;...

The Issue: Non-Sterility; contract laboratory identified Staphylococcus warneri in the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 13, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL) Recalled by...

The Issue: Failed Impurity/Degradation Specifications; out of specification value for...

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

Class III — Low RiskOngoing
Refund
DrugMay 13, 2013· Zydus Pharmaceuticals USA Inc

Recalled Item: Warfarin Sodium Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Failed Tablet/Capsule Specifications: A product complaint was received from...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 10, 2013· Apotex Corp.

Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Corp. Due to...

The Issue: Crystallization: Potential to exhibit precipitation/crystallization in IV...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510121 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510613 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510613 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Rauland-Borg Corp

Recalled Item: Responder 5 is a nurse call communication system that connects Recalled by...

The Issue: A counterfeited electronic component was identified in the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510031 Disposable Single Infusion Pump Recalled by Symbios Medical...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510450 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part510447 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510490 Disposable Infusion Pump Recalled by Symbios Medical Products,...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510180 Disposable Single Infusion Pump Recalled by Symbios Medical...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· SpineFrontier, Inc.

Recalled Item: Invue Split Driver Recalled by SpineFrontier, Inc. Due to Device design.

The Issue: Device design.

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

Class II — Potential Health HazardOngoing