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 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Whole Foods Organic Raw Almonds Imported from Spain USDA Organic; Net WT. 13.5 oz. (383 g) plastic tub; Ingredients:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Marin Food Specialties Inc.
FDA (openFDA food enforcement)
Reported Jan 14, 2015
Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abdallah Candies, Inc.
FDA (openFDA food enforcement)
Reported Jan 14, 2015
Lumbar Extension Machine for Physical Therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MedX Holdings, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 7, 2015
MRS FRIDAY'S GOURMET BREADED MEDIUM OYSTERS 18/25 CT/LB, Net Wt. 2.5 lbs (1.13 kg), Ready to Fry, Distributed by: King…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King & Prince Seafood
FDA (openFDA food enforcement)
Reported Dec 31, 2014
Private Selection Extreme Moose Tracks Ice Cream; packaged in plastic 48 fl oz containers, UPC Code: 11110-00456
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
FDA (openFDA food enforcement)
Reported Dec 24, 2014
RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2014
Additional devices identified in new FSN MA-FCO 83000190: QLAB versions 10.0 with a2DQ and/or aCMQ plug-ins installed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2014
MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
LUNA Chest, Model No. LU4006
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novadaq Technologies, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
BrightView product code: 882478 BrightView X product code: 882480 BrightView XCT product code: 882482 and 882454
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2014
The MectaLIF Oblique Handle, model number 03.22.10.0262, is used to insert the MectaLIF oblique spinal cage implants.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA
FDA (openFDA device enforcement)
Reported Nov 19, 2014
Transport Rollator with Padded Seat; Large 8-inch wheels with wheel locks (indoor and outdoor use), fold down…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roscoe Medical Inc.
FDA (openFDA device enforcement)
Reported Nov 19, 2014
The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Nov 19, 2014
365 Organic Raisin Granola in 17 ounce (482 gram) cardboard cartons; 12 cartons per case. UPC: 099482448738
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market Brand 365, LLC
FDA (openFDA food enforcement)
Reported Nov 12, 2014
Siemens Calibrator E; SMN 10309079 (2 pack), SMN 10321075 (6 pack), SMN 10335532 (6 pack Ref)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
DMI Duro-Med Industries Rollator Transport Chair; Wheel Size: 7 1/4"; Overall Width: 23 1/2"; Seat Height: 21 1/4";…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Briggs Medical Service Company d.b.a. Mabis
FDA (openFDA device enforcement)
Reported Nov 5, 2014
Family Gourmet Long Grain Enriched White Rice in 32 oz. clear plastic bags (SKU: 1218898) and 80 oz. clear plastic bag…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Family Dollar Stores - NC Distribution Center
FDA (openFDA food enforcement)
Reported Nov 5, 2014
The GemStar Power Supply is an accessory for the GemStar Infusion Pump. It is a two piece assembled switching power…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2014
ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Accu-Chek Combo System Product Usage: The ACCU-CHEK Combo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
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.