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.
2,138 stored notices name Idaho, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Idaho too — those are in the archive.
Reported Jul 8, 2020
Maestro Orthodontic Bracket REF711-206-10 QTY. 10 Rx Only (01)00190707016517 (10)112233 (422)484
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho Organizers, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is intended for use in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer SMN #10380062 - Product Usage: are intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2020
Atellica Solution IM1300 Analyzer, Siemens Material Number 11066001, UDI # 00630414007960
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 28, 2020
Pilgrim's Pride Corporation Recalls Chicken Breast Nugget Products due to Possible Foreign Matter Contamination
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pilgrim's Pride Corporation
USDA FSIS
Reported Jun 24, 2020
PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2020
VITROS Chemistry Product AMYL Slides Reagent, AMYLASE/5 PACK/300 SLDS, Product Code 1202670, UDI # 10758750008513 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inari Medical
FDA (openFDA device enforcement)
Reported Jun 17, 2020
STAINLESS STEEL REPROCESSING TRAY, 8MM ENDOSCOPE, IS4000, Model No. 400498-02 - Product Usage: is designed to enable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Mazor X Surgical System Positioner Type II, REF: ASM0214-02
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Infant/Child Reduced Energy Defibrillation Electrodes, Part Number: 3202380-006, for use with LIFEPAK 1000…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
ADVIA Chemistry Fructosamine Reagent (FRUC), Siemens Material Number 10361941, UDI Number 00630414558073 - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Beckman Coulter Access Immunoassay Systems, Access Free T4 Thyroxine, REF 33880 (UDI:15099590225834) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Pressure Monitoring Set, C-PMS, G02838
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
NobelActive Internal NP 3.5x15mm Endosseus dental implant, REF: 34128, Rx Only, Sterile R, CE, UDI: (01)07332747010619
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nobel Biocare USA LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2020
ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained are used in the diagnosis and treatment of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Panther Fusion Extraction Reagent-S, Ref PRD-04331, IVD, CE, Rx Only consisting of FCR-S Fusion Capture Reagent - S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
GENTLEWAVE REF: FG-002-0001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonendo Inc.
FDA (openFDA device enforcement)
Reported May 27, 2020
STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The device is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2020
Frames Direct Prescription Spectacle Lenses included in the frame brands
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frames Direct
FDA (openFDA device enforcement)
Reported May 20, 2020
BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND" ED Quick Kit 3FR 6cm. REF/UDI 72627/ 00859821006674 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Access Scientific LLC
11 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.