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.
1,993 stored notices name New Mexico, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach New Mexico too — those are in the archive.
Reported Jun 21, 2023
Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992206 Version A, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Icelock 125 Ratchet, REF: L-125000; Icelock 600XM Ratchet, REF: L-621200; Icelock 621 Ratchet, REF: L-621000; Icelock…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
FDA (openFDA device enforcement)
Reported Jun 14, 2023
Elekta Unity Image-Guided Radiation Therapy System containing an MR gradient coil.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 7, 2023
Black Fungus Golden Koi 2.5 oz packages 100 bags per case UPC: 81005681145 Product of China
High riskUsing this product could cause serious injury, illness or death — stop using it now.AH USA Group Inc.
FDA (openFDA food enforcement)
Reported May 31, 2023
Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-048143026143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Outdoor Products, Inc.
FDA (openFDA food enforcement)
Reported May 31, 2023
Copitas; small ceramic cups; "Del Maguey" embossed on the bottom; distributed by Del Maguey
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pernod Ricard USA Inc.
FDA (openFDA food enforcement)
Reported May 31, 2023
truCONTROL 60 Count
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TruVision Health LLC
11 more products in this recall
FDA (openFDA food enforcement)
Reported May 24, 2023
Beckman Coulter Bicarbonate, REF: OSR6137, 4x25 mL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported May 17, 2023
BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2023
Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZB Importing LLC
FDA (openFDA food enforcement)
Reported May 10, 2023
SafeLight Fiber Optic Cable: Clear, 5MM X 10FT 3.05M, REF: 0233-050-100; Gray, 5MM X 10FT 3.05M, REF: 0233-050-200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported May 3, 2023
(1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3.5cm); and (2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported May 3, 2023
HAMILTON-C6, REF: 160021
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported May 3, 2023
G5300 Lamb's Supreme Hash Brown Patties, Frozen, 24 patties packed in blank unlabeled tray, 12 trays packaged in one…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lamb Weston Sales
FDA (openFDA food enforcement)
Reported Apr 26, 2023
Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, and Cuffless: Disposable Inner Cannula or Reusable Inner…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Apr 26, 2023
AQURE REF 933-599 Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 The AQURE system is intended to let you manage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Edward Lifesciences, REF 777F8, Swan-Ganz CCOmbo V, CCO/SvO2/CEDV/VIP, Thermodilution Catheter, Exterior Diameter 8F…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 19, 2023
Kagome Worcester Sauce 6/60 fl oz. Ingredients: Water, Sugar, Salt, Fermented Vinegar, Glucose, Tomato Extract, Caramel…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mutual Trading Company Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 19, 2023
Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a next generation, self-contained hemodialysis system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Instructions for Use for the following Leksell Stereotactic System and Leksell Neurosurgical Instruments: (1) Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Instrument AB
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Mar 29, 2023
BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
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.