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.

1,959 stored notices name New Mexico, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.

Medical devices

Reported Jan 10, 2024

Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B…

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

Philips Respironics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

Alinity ci-series System Control Module, REF: 03R70-01

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

Injection Needle, REF: 25207

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

Karl Storz Endoscopy

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…

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

Nurse Assist, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

LITe Decompression Snake Arm, REF 48080230

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

Stryker Spine

FDA (openFDA device enforcement)

Food

Reported Dec 20, 2023

Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection

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

Houdini Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 13, 2023

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vitro diagnostic for blood ketone values.

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

Stanbio Laboratory, LP

FDA (openFDA device enforcement)

Medical devices

Reported Dec 6, 2023

BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533

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

Becton Dickinson Infusion Therapy Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 6, 2023

Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…

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

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

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

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to…

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

SunMed Holdings, LLC

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.

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

Abbott Laboratories

FDA (openFDA food enforcement)

Medical devices

Reported Nov 15, 2023

BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.

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

Breg Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

BD Alaris PCU REF 8015

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU 900260

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

Family Dollar Stores, Llc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

Gills Onions 3 lb. bags, diced yellow onions

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

Gills Onions, LLC

72 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 15, 2023

StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 15, 2023

Nutricia KetcoCal 4:1 LQ Unflavored in 237ml (8fl oz) packaged in tetra prisma paper aseptic carton - 3 cartons per box…

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

Nutricia North America

FDA (openFDA food enforcement)

Medical devices

Reported Nov 1, 2023

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

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

Cardinal Health 200, LLC

5 more products in this recall

FDA (openFDA device enforcement)

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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.