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.
2,142 stored notices name Idaho, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Idaho too — those are in the archive.
Reported Jan 15, 2020
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TFI Holding dba Grey Ghost Bakery
FDA (openFDA food enforcement)
Reported Jan 8, 2020
Chicken of the Sea Sardines in Water; Net Wt. 3.75 oz. (106g) UPC 0 48000 00707 0 18 Individual items per case…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Chicken of the Sea
FDA (openFDA food enforcement)
Reported Jan 8, 2020
O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK GUIDE SAMPLE KIT MG/DL - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
High riskUsing this product could cause serious injury, illness or death — stop using it now.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
41 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Quantam 2000 Electrosurgical Generator, Part number 909075.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 11, 2019
Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 1PRT(Single Port) Quick Connect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Alinity ci Level Sensor, Bulk Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Ready to eat Pip Pop Movie Theater Popcorn packaged in 24 oz. laminated plastic zip pouch bag, 6 per case, UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Water Gardens Confections LLC
FDA (openFDA food enforcement)
Reported Nov 27, 2019
EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Arroyo Grande California Cilantro; Talley Farms; Product of USA - 30 or 60 Count Individual bunches tied with Talley…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Talley Farms
FDA (openFDA food enforcement)
Reported Nov 20, 2019
Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cadence Science, Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2019
Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Prismaflex Control Unit, software versions below 7.21
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 13, 2019
Giraffe OmniBed Carestation CS1 - Product Usage: The device can be operated as an incubator or as a warmer and can…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 13, 2019
The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 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.