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. 1,839 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,839 in last 12 months

Showing 2690126920 of 27,850 recalls

Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: Stryker MANTIS TORQUE WRENCH Manufactured by: Stryker pine Recalled by...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Integra LifeSciences Corporation

Recalled Item: Integra CRW Precision Arc (CRWPRECISE) Recalled by Integra LifeSciences...

The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Integra LifeSciences Corporation

Recalled Item: Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW Recalled by...

The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Embolectomy Catheters (Models A44XX Recalled by Applied Medical Resources...

The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Irrigation Catheters (Models IRR-XXX-XX): Model Numbers & Description:...

The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Stryker Spine

Recalled Item: SPECIALTY AUDIBLE TORQUE WRENCH Recalled by Stryker Spine Due to Multiple...

The Issue: Multiple complaints have reported the hex tip of the torque wrench...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Applied Medical Resources Corp

Recalled Item: Biliary Catheters (Models A47XX and CB0XXXXX): Model Numbers & Description:...

The Issue: Applied Medical is recalling specific lot numbers of its Vascular Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· AGFA Corp.

Recalled Item: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and Recalled by AGFA...

The Issue: Loss of patient data can occur under certain circumstances due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Positron Emission Tomography (PET) and X-ray Computed Tomography Recalled by...

The Issue: Philips became aware of an issue relating to a UPS battery cabinet that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2012· Parks Medical Electronics, Inc

Recalled Item: Devices includes a Multi Port Inflator or without Multi Port Recalled by...

The Issue: Parks Medical Electronics, Inc. was made aware of two incidents where an air...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...

The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 6, 2012· Elekta, Inc.

Recalled Item: Precise Digital Accelerator Delivery of radiation to defined target volumes...

The Issue: There have been a small number of instances in hospitals where the joint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Invacare Corporation

Recalled Item: Invacare¿ I-Fit" Shower Chair (Models 9780 Recalled by Invacare Corporation...

The Issue: On August 6, 2012, Invacare voluntarily recalled the Invacare¿ I-Fit" Shower...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· ThyssenKrupp Access Corp

Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...

The Issue: The seat could break as a result of damage resulting from a seat belt being...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Diamedix Corporation

Recalled Item: The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The...

The Issue: Diamedix Corporation recalled their Is-anti-Sm Test Kit due to the Positive...

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

Class II — Potential Health HazardOngoing