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 22, 2021
The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 15, 2021
Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ingredion
FDA (openFDA food enforcement)
Reported Sep 15, 2021
Pipeline Flex Embolization Device
High riskUsing this product could cause serious injury, illness or death — stop using it now.Micro Therapeutics Inc.,
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 15, 2021
Trader Joe's Super Spinach Salad with Quinoa, carrots, cranberries, chickpeas, edamame, pumpkin seeds and a carrot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.World Class Distribution, Inc.
FDA (openFDA food enforcement)
Reported Sep 8, 2021
Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 8, 2021
CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMimetic Therapeutics, LLC
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W. L. Gore & Associates Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
CIRCUL8 LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF: 08-0020, Rx Prescription Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho8, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
ACCESS SARS-CoV-2 Antigen , REF: C68668, IVD, Rx only, UDI: (01) 15099590742713;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec, Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Iherb LLC
FDA (openFDA food enforcement)
Reported Aug 18, 2021
Medtronic StimLoc Burr Hole Cover, Part Numbers: a) 3387S-40 b) 3389S-28 c) 3389S-40 d) 3391S-40 e) 3550S-01 f) 924256…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 11, 2021
REF: 08P1820, Abbott Alinity c Activated Alanine Aminotransferase reagent Kit, Alinity c Activated Alanine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 11, 2021
Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stanbio Laboratory, LP
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 11, 2021
GlideScope Go Monitors
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Amy's Bowls, Tortilla Casserole & Black Beans; Made with organic tomatoes & Black Beans. NET WT 9.5 oz. (269g); gluten…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amys Kitchen Inc.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Health Group Inc.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sunrise Medical (US) LLC
1 more product 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.