All recall categories

Recalls distributed in New Mexico

These notices name New Mexico in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

1,993 stored notices name New Mexico, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.

Food

Reported Mar 29, 2023

DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Dollar General Corporation

FDA (openFDA food enforcement)

Food

Reported Mar 22, 2023

Egg roll wrappers, 6" x 6" and 7" x 7", packaged in 30lb. corrugated (cardboard) boxes. Product is sold frozen.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Baily International Foods

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 22, 2023

Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 22, 2023

Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Keurig Dr Pepper

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2023

Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DiaSorin Molecular LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 15, 2023

Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Given Imaging Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2023

Sensus Healthcare Inc, SRT-100 Vision IPX 0, HFUS Module IPX 1, with software version 1.9.2; Superficial X-ray…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sensus Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2023

Ultracell Wick with 80cc Collection Bag, 20/box

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beaver Visitec International, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2023

Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2023

The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 8, 2023

Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

BD Pyxis MedBank System - Product Label/labeling pending

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

RadiaLux Lighted Retractor (Pink), REF: 50-101-1

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ventana Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2023

Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Acumed LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 4, 2023

Premium Quality Shirakiku Fish Sausage Original Net wt. 9.8 oz. (280g) UPC 074410366414 Ingredients: Fish meat (bream,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Wismettac Asian Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bunnell, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

Hamilton-C6

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hamilton Medical AG

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2022

Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2022

Hill-Rom Progressa Bed System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2022

Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 16, 2022

ReadyMeals Chicken Salad Quad, 12 oz., in a clear plastic container with four compartments, UPC 2 1352 40000 0,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Albertsons Companies LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 16, 2022

Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Avanos Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 16, 2022

Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6 91355 89889 5, Manufactured for: Hammond's Candies, 5735…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hammond's Candies Since 1920 II, LLC

FDA (openFDA food enforcement)

Free recall alerts

Get alerted about new New Mexico recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.