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 Oct 28, 2020

Langston Dual Lumen Catheter

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

Vascular Solutions, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 21, 2020

Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI -…

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

Mizuho OSI

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2020

PermaFlo Flowable Composite REF-UP 948 Shade: A2 - Product Usage: is a light cured, radiopaque, methacrylate based,…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2020

Pacific Xtreme (PTCA Balloon Dilation Catheter)

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

ev3 Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2020

Control, Calibrator Verified, Triage BNP, Model ALR88755

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2020

BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol, REF 33570.

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 30, 2020

Lay's Barbecue Flavored Potato Chips 1 oz. UPC 28400 00861; Lay's Barbecue Flavored Potato Chips 1 1/2 oz. UPC 28400…

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

Frito-Lay, Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 30, 2020

Trader Joe's Southwest Style Sweet Potato Saut¿ Bowl NET WT. 21.05oz (1 LB 5.5 OZ) 610g UPC 00661126 packaged in a…

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

Renaissance Food Group LLC

FDA (openFDA food enforcement)

Food

Reported Sep 23, 2020

Spicy Beef & Vegetables with Rice & Sesame Seeds meal kits containing onions delivered the week of July 27, 2020.

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

Blue Apron Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2020

The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…

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

Life Technologies Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2020

NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…

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

Novarad Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2020

BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…

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

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 16, 2020

Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.

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

Hellofresh US

FDA (openFDA food enforcement)

Medical devices

Reported Sep 16, 2020

Merge PACS

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

Amylase AY3805 batch 480449 Amylase Ethylidene Blocked-pNPG7 Reagent

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

Randox Laboratories, Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…

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

Stimwave Technologies Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…

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

Biosense Webster (israel), Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…

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

Karl Storz Endoscopy

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coated Micro-Plate-IVD…

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

OraSure Technologies, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of…

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 Aug 26, 2020

Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate…

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

CareFusion 303, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2020

MURRAY'S CHADS SMOKED GOUDA DIP in plastic tubs, all sizes.

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

The Kroger Co.

16 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2020

Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…

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

Luminex Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2020

Kouign-Amann Pastry available in plastic clamshell 4-packs with Whole Foods Market scale labels, a PLU code 26739400000

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

Whole Foods Market

FDA (openFDA food enforcement)

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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.