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.

1,996 stored notices name New Mexico, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.

Food

Reported Apr 3, 2019

Jacques Big Daddy Dark Chocolate Bar. The product comes in un-coded 2.2 lbs. (1kg) clear plastic package overwrapped…

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

Jacques Torres Manufacturing , llc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 3, 2019

Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)…

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

Medical Action Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 20, 2019

Zarrin Pickled Cucumbers & Cornichons: Net Weight 101.4 oz. 3 kg. Ingredients: Cucumber, water, salt, acid (acetic…

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

Kradjian Importing Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 20, 2019

VITROS Chemistry Products Na+ Slides, Catalog Number 8379034 For in vitro diagnostic use only. VITROS Na+ Slides…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Mar 20, 2019

Ossur Skull Pin, Sterile Titanium Pin, Part/Description: 516TS/ Skull Pin 2-1/4in TI Sterl 1PK; 516V2S/ Skull Pin 3in…

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

Ossur Americas

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 20, 2019

AMSCO 3000 Series Washer/Disinfector Model # 3052

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2019

BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2019

Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic…

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

Alcon Research Laboratories Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Phoenix AST-s Indicator, Catalog Number 246009

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

Becton Dickinson & Co.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2019

Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold…

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

King Orchards

FDA (openFDA food enforcement)

Food

Reported Mar 6, 2019

Nita Crisp Spelt Bread Cracker, 8- & 16-ounce bags, In paper bags with a plastic window and has a re-closable ability…

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

Nita Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 27, 2019

AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…

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

Diamond Crystal Brands, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with…

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

Bard Medical Division

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The…

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

Handpiece Headquarters

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

Product: ABL800 FLEX with Crea. The ABL800 with Crea is available in the following configurations: ABL817, ABL827 and…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 30, 2019

Perfusion Pack, Rx only, Sterile EO

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

LivaNova USA

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

Siemens Biograph Horizon PET/CT System, Product Usage: The Siemens Biograph systems are combined X-Ray Computed…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 2, 2019

Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10mL Injectable Solution, 1 mg/10 mL incorrectly labeled as…

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

Advanced Pharma Inc.

FDA (openFDA drug 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.