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. 1,006 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,006 in last 12 months

Showing 20801–20820 of 48,595 recalls

Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Drive Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Qiagen Sciences LLC

Recalled Item: QIAsymphony SP SOW 5.0.3 Recalled by Qiagen Sciences LLC Due to QIAsymphony...

The Issue: QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151810 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151815 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151813 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Blanketrol II Hyper-Hypothermia System Recalled by Cincinnati Sub-Zero...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric...

The Issue: The firm conducted internal investigations that confirmed customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151814 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: CVS Health Preservative Free Lubricant Eye Drops (Carboxymethy-Cellulose...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets (0.8...

The Issue: Failed Impurities/Degradation Specifications: Kaitlib Fe Tablets has an out...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Altacaine (Tetracaine Hydrochloride) Ophthalmic Solution Recalled by Altaire...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Altaire Sterile Eye Wash Recalled by Altaire Pharmaceuticals, Inc. Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2019· Altaire Pharmaceuticals, Inc.

Recalled Item: Perrigo Neomycin and Polymixin B Sulfates and Dexamethasone Ophthalmic...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund