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. 1,849 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,849 in last 12 months

Showing 2588125900 of 27,850 recalls

Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N8371: Non-DEHP Y-Type Catheter Extension Set Kit Recalled...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Suturable DuraGen Dural Regenerative Matrix Suturable DuraGen Dural...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Custom Spine, Inc.

Recalled Item: Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 Recalled by Custom...

The Issue: On March 28, 2013, Custom Spine, Inc. issued a minor removal of a lot of 18...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: DuraGen Plus Dural Regeneration Matrix DuraGen Plus Adhesion Barrier Matrix...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: OraTape Absorbable Collagen Wound Dressing for Dental Surgery The Absorbable...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Transonic Systems Inc

Recalled Item: HCS3011 AV Loop Kit For use with Transonic CO status System Only Recalled by...

The Issue: Transonic Systems Inc. have received complaints of blood leakage involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: INSTAT - Agent Recalled by Integra LifeSciences Corporation Due to Due to...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Ora Plug Absorbable Collagen Wound Dressing for Dental Surgery The Recalled...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Elekta, Inc.

Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...

The Issue: The problem is that the "static tolerances" from the calibration files...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Abbott Molecular

Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...

The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...

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

Class III — Low RiskOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: HeliTape Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Dural Graft Matrix DuraGen¿ Dural Graft Matrix is an absorbable Recalled by...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Colla Tape Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Helistat Absorbable Hemostatic Recalled by Integra LifeSciences Corporation...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N1191: Non-DEHP Y-Type Catheter Extension Set Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: BioMend¿ Extend" Absorbable Collagen Membrane BioMend¿ Extend" Absorbable...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Helitene Absorbable Collagen Hemostatic Sponge Helitene is indicated in...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Corp. AxSOS System Instrument. The AxSOS Locking...

The Issue: Stryker Orthopaedics has received a report indicating that the scale of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing