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.

1,994 stored notices name New Mexico, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.

Medical devices

Reported Nov 25, 2020

COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…

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

Merz North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 25, 2020

Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.

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

Thomas Scientific

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…

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

Aesthetics Biomedical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of…

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

Epitope Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 18, 2020

J&O Mixed Veggie Cup with Dip, Net Weight 5.0 oz. (128 g), UPC 95631-85818. Mfg By: RDW, Pueblo CO 81001

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

Russ Davis Wholesale, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 18, 2020

Niobe ES System, Models 001-006000-1 and 001-006100-1

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

Stereotaxis Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to…

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

GE Healthcare, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051;…

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

ICU Medical, Inc.

98 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to be used with an Olympus TV camera system, light…

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay…

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 28, 2020

Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

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)

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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.