Recalls distributed in Idaho
These notices name Idaho 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.
2,107 stored notices name Idaho, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Idaho too — those are in the archive.
Reported Sep 13, 2023
ISee Ortho-K Lens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PARAGON VISION SCIENCES, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 6, 2023
epoc BGEM BUN Test Card with epoc Host SW v3.37.3, epoc NXS SW v4.10.6, Sensor Configuration 41.1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 16, 2023
HoverMatt, 39" W x 78" L, REF: HM39SPU-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Aug 9, 2023
Caesar Pasta Salad is a food service refrigerated product, packaged in 5lb flexible plastic packages, 2/5lb. packages…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eat Good LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 9, 2023
OEC Flexiview 8800 Systems with 9-inch Image Intensifier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2023
The following Pro.specta Emission Computed Tomography Systems that were manufactured with an SLD Look Ahead Optical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2023
HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
QIAstat-Dx¿ Respiratory SARS-CoV-2 Panel -IVD intended for the detection and differentiation of nucleic acid from…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Simplexa Direct Amplification Disc Kit, Rx Only, IVD The Simplexa Direct Amplification Disc Kit, REF: MOL1455 is 1 box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Jul 19, 2023
Great Value Sliced Strawberries. Item # 107356. Frozen, packaged flexible plastic bags. Net wt. 4 lbs (64oz). UPC on…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oregon Potato Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2023
BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2023
Exactech Shoulder GPS Impactor Handle, Catalog #531-07-05.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 5, 2023
LEGACY SMARTBASE, NE 3.0D 1MML, REF: 8730-81NE; LEGACY SMARTBASE, NE 3.0D 2MML, REF 8730-82NE; LEGACY SMARTBASE NARROW…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing LLC
FDA (openFDA device enforcement)
Reported Jun 28, 2023
Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale [Model(s): RW82VHA-1, RW82VHA-1C, RW82VHA-1D,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 28, 2023
enterade Advanced Oncology Formula; Original Vanilla Flavor; Medical Food; Helps manage and maintain GI function; 8 FL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Entrinsic Health Solution Inc.
FDA (openFDA food enforcement)
Reported Jun 28, 2023
KARL STORZ Radel Sterilization Trays, Models: 27717A, 27717B, 39301A, 39301C, 39231XA, 39301C1, 39311A, 39317A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 28, 2023
Masimo RD Set TC-I SpO2 Adult Reusable Ear Sensor, REF: 4053
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Masimo Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion Indirect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
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 21, 2023
Recalled product has the carton labeled as Tillamook 1.5 QT CHOCOLATE PEANUT BUTTER Ice Cream, frozen, 1.5 Qt. and has…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tillamook County Creamery Association
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)
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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.