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.
Reported Nov 28, 2018
The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Roasted Corn Salsa; Net Weight: 10 lbs. (10 x 1 lb. bags) Corner Bakery Caf¿ Brand Ingredients: Corn, Red Onion,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cadence Gourmet LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 21, 2018
bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2018
GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 21, 2018
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2018
VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Nov 14, 2018
TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2018
EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…
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)
Reported Nov 7, 2018
BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable Bone Growth Stimulator is indicated in the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
BACT/ALERT VIRTUO system, A Unit, with Version R2.0 Firmware Product Usage: The BacT/ALERT VIRTU Microbial Detection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Callie's Charleston Biscuits
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 31, 2018
Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Cedar's Chickpea Salad, packaged in an 8oz plastic container, UPC: 044115337767. Product is refrigerated.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cedar's Mediterranean Foods, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 31, 2018
Mitek Screw and Washer Depth Gauge, Product Code 219024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ecolab Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
MyLab Alpha, Model 7400
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Esaote S.p.a.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
APTIO INPUT/OUTPUT MODULE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
3.0mm Headless Compression Screw, Long Thread 18mm, Part Number 04.226.118 DePuy Synthes 3.0mm Headless Compression…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Oct 24, 2018
GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OriGen Biomedical, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Switzerland GmbH
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of fractures
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
47 more products in this recall
FDA (openFDA device 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.