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

48,595 total recalls
980 in last 12 months

Showing 28541–28560 of 48,595 recalls

Medical DeviceMay 9, 2017· Covidien LLC

Recalled Item: Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: Recalled by...

The Issue: Cotton tip of the device may disengage due to insufficient adhesive

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Cook Inc.

Recalled Item: Cook Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Correction...

The Issue: Correction to the product Instructions for Use because the current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arrow Pressure Injectable PICC Kit Catheter Recalled by Arrow International...

The Issue: The Arrow Pressure Injectable PICC is intended for short-term or long-term...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended Recalled by...

The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) Introducer Kit with Integral Hemostasis Valve/Side Port Recalled by Arrow...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
DrugMay 9, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Montelukast Sodium Oral Granules Recalled by Mylan Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications; out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMay 9, 2017· Strides Pharma INC

Recalled Item: Benzonatate capsules Recalled by Strides Pharma INC Due to Failed Stability...

The Issue: Failed Stability Specifications: Out of Specification results obtained for...

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

Class III — Low RiskOngoing
Refund
DrugMay 8, 2017· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCORTISONE LOTION Recalled by Vintage Pharmaceuticals LLC, DBA Qualitest...

The Issue: Superpotent Drug: above specification for the assay.

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

Class III — Low RiskOngoing
Refund
FoodMay 8, 2017· Fourth Street Barbeque, Inc.

Recalled Item: Pick 5 Chicken & Waffle Sandwich Recalled by Fourth Street Barbeque, Inc....

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2017· RB Manufacturing LLC

Recalled Item: Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine +...

The Issue: RB Manufacturing is recalling Move Free Advance Tablets due to incorrect...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...

The Issue: When cut lines are shown on an image, the lines may go from being vertical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...

The Issue: Merge PACS did not show unviewed images when the last view was skipped....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Reusable instruments in the Knee Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Durability characteristics of reusable instruments were not established

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Alphatec Spine, Inc.

Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...

The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Recalled...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· GE Healthcare, LLC

Recalled Item: Infant Warmer System (IWS) Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Herpes Simplex Virus I Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Her2/Neu (EP3) Recalled by Cell Marque Corporation Due to Cell Marque has...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing