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. 2,605 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,605 in last 12 months

Showing 22212240 of 27,850 recalls

Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate Recalled by...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H LT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO...

The Issue: Due to an error message that prevents users from utilizing carboxyhemoglobin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Physio-Control, Inc.

Recalled Item: LIFEPAK 35 ECG cable Recalled by Physio-Control, Inc. Due to Product shipped...

The Issue: Product shipped with incorrect IFU. IFU does not include proper...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2025· Microbiologics Inc

Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Control Panel...

The Issue: Internal quality control procedures were not followed correctly for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2025· Microbiologics Inc

Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Verification Panel...

The Issue: Internal quality control procedures were not followed correctly for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2025· Zhejiang Luyao Electronics Technology Co., Ltd.

Recalled Item: Brand Name: HOMEDICS Product Name: Air Compression Leg Massager...

The Issue: Regulatory documentation error and misleading color packaging claim.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2025· KCI USA, INC.

Recalled Item: 3M V.A.C. VIA Negative Pressure Wound Therapy System /US Recalled by KCI...

The Issue: Due to increase in complaints related to leak alarms

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2025· KCI USA, INC.

Recalled Item: 3M Prevena Plus 125 Therapy Unit and System Kits by KCI USA, INC. Due to Due...

The Issue: Due to increase in complaints related to leak alarms

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2025· Spectrum Medical Inc

Recalled Item: Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated...

The Issue: Their is a potential of fluid leakage from the centrifugal blood pump pump...

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

Class II — Potential Health HazardOngoing