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 Dec 25, 2019

Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…

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

Allergan PLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive cream for use with external electrodes -…

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

Bio-Signal Group Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2019

Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is…

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

Rhondium Limited

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Healix Knotless ADV BR 4.75 Suture Anchor

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

DePuy Mitek, Inc., a Johnson & Johnson Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096

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

Encore Medical, LP

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2019

Terra Alba Calcium Sulfate Dihydrate packaged in 50 lb. bags; 25 lb. bags; 800kg (1764 lb.) bulk bags; 2000 lb. bulk…

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

Harrison Gypsum, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 18, 2019

VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2019

Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943

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

Medtronic Navigation, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2019

Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin…

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

Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2019

Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs,…

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

Frog Hollow Farm

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2019

TLC-2000 Therapeutic Medical Laser System, used for the temporary relief of knee pain.

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

Theralase Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2019

Atellica CH 930 Analyzer

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2019

EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

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

Baxter Healthcare Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2019

Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.

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

Dollar General Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2019

Giraffe OmniBed Carestation CS1 - Product Usage: The device can be operated as an incubator or as a warmer and can…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.

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

Teleflex-Morrisville

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For fracture fixation or reconstruction of the sternum.

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

Alto Development Corp.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…

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

Stryker Neurovascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2019

Posey Connected Twice-As-Tough Cuffs

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

Tidi Products

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2019

Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole Packaged Foods, LLC Westlake Village, CA 91361…

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

Dole Packaged Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2019

ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…

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

GE Healthcare, LLC

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.