Recalls distributed in Oregon
These notices name Oregon 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.
3,297 stored notices name Oregon, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Oregon too — those are in the archive.
Reported May 3, 2017
BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) and Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitaleX)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported May 3, 2017
ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 3, 2017
Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosoft, Inc. dba Zimmer CAS
FDA (openFDA device enforcement)
Reported May 3, 2017
uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ulrich Medical USA Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9
High riskUsing this product could cause serious injury, illness or death — stop using it now.Advanced Fresh Concepts Corp.
FDA (openFDA food enforcement)
Reported Apr 26, 2017
NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ashers Chocolates/Lewistown, Inc.
86 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Software version 4.44A utilized on the BD MAX System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Life Sciences
FDA (openFDA device enforcement)
Reported Apr 26, 2017
SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien Medtronic
FDA (openFDA device enforcement)
Reported Apr 26, 2017
PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CP Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nutiva
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 26, 2017
French's Crispy Jalapenos Net Wt. 5 oz. (141.7g), UPC 0 41500 95309 0, French's Food Company.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The French's Food Company, LLC SUBS Reckitt Benckiser
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Venison Jerky, brand Trophy Series, heat treated shelf stable packaged in hermetically sealed packages. Net wt. 3 oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whiskey Hill Smokehouse
3 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 19, 2017
VIDAS Estradiol II, Ref 30431-01, 60 tests The VIDAS Estradiol II (E2 II) assay is intended for use on the instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Assorted Bonbons are molded chocolates with ganache fillings in assorted flavors, No package weight. Product packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dolcetta Artisan Sweets
25 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 19, 2017
Specimen Gate Laboratory; Product Number: 5002-0180 Specimen Gate Laboratory is intended for use as a data processing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 19, 2017
CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Apr 12, 2017
DX-D600 - DXD Imaging Package
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Apr 12, 2017
Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ikea North America Srvcs Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 12, 2017
Mobile Diagnostic X-Ray System with Digital Panel
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Oregon recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.