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 48,122 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.

Food

Reported Apr 22, 2015

PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle

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

ReNew Life Formulas, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2015

CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic…

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

Carestream Health, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

ToggleLoc; fastener, fixation, non degradable, soft tissue; Artificial Ligament Fixation Device #7 PE Ziploop Extended…

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

Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2015

Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a…

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

Gilster-Mary Lee Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2015

Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…

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

Medtronic Inc. Cardiac Rhythm Disease Management

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence technology, Brilliance iCT, Brilliance iCT SP,…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2015

Mini Naan Eight (8) nann packaged in coated paper printed board and transparent wrap with a net weight of 12.6 oz (360…

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

fgf brands, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 1, 2015

Natural Grocers brand Organic Garlic Powder. Natural Grocers brand Organic Garlic Powder. Packaged in Zip-Lock-type…

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

Vitamin Cottage Natural Food Markets, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 25, 2015

Crea A and B membranes, packaged 4 per box Used in conjunction with the ABL800 FLEX analyzers which are intended for:…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2015

Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2015

CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.

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

Smiths Medical ASD, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2015

TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias…

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

St Jude Medical

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2015

GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of…

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

GE Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2015

Monaco radiation therapy treatment planning system. The Monaco system is used to make treatment plans for patients with…

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2015

KimVent Closed Suction System for Adults, Double Swivel Elbow, 12 Fr., Sterile, Distributed by Kimberly Clark Global…

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

Halyard Health

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 4, 2015

Adams Pantry Basics Chili Powder Net Wt. 2.82 oz (80 g) UPC: 041313017224; Adams Pantry Basics Value Size Chili Powder…

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

Adams Extract & Spice LLC

44 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2015

The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2015

CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of…

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

Zimmer GmbH

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2015

Cold Therapy Pad - cold water circulating pad, one unit per package. The pads are used to provide a patient with local…

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

Cincinnati Sub-Zero Products Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 25, 2015

Caramel Apples packaged in the following configurations with Best By date range - 8/25-11/23/2014, Responsible firm…

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

Lochirco Fruit & Produce Inc.

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 18, 2015

The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…

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

Integra LifeSciences Corporation

FDA (openFDA device enforcement)

Food

Reported Feb 18, 2015

MorningStar Farms Spicy Black Bean Burger: 9.50 oz (4 ct) - UPC 2898939207; 18.90 oz (8 ct): UPC 2898971750; 8.7 lb…

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

Kellogg USA Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 18, 2015

Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.

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

Virtual Imaging, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2015

Baxter Integrated APD Set with Cassette 3-Prong, Sterile, nonpyrogenic fluid path. Product Usage: The recall device is…

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

Baxter Healthcare Corp.

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.