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.
3,336 stored notices name Oregon, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Oregon too — those are in the archive.
Reported Apr 16, 2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.MEDLINE INDUSTRIES, LP - Northfield
10 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 9, 2025
BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Apr 9, 2025
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Apr 9, 2025
Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle-USA, Inc. (Corporate Office)
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 2, 2025
CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Calyxo, Inc.
FDA (openFDA device enforcement)
Reported Apr 2, 2025
Brand Names: MyDay Toric, LensCrafters One Day Premium Daily Disposable Contact Lenses For Astigmatism, Pearle Vision 1…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperVision, Inc.
FDA (openFDA device enforcement)
Reported Apr 2, 2025
CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital System Model CM3100 -CardioMEMS Backend Web…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical
FDA (openFDA device enforcement)
Reported Apr 2, 2025
DRIED LILY FLOWERS Net Weight 2.5 oz (70g) Ingredients: Lily flower (Hemerocallis citrina) Distributed by: U.S. TRADING…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.U.S. Tov, Inc. dba U.S. Trading Company
FDA (openFDA food enforcement)
Reported Apr 2, 2025
NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Mar 31, 2025
FSIS Issues Public Health Alert for White Chicken Chili Imported Without the Benefit of Import Reinspection
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Mar 26, 2025
BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2025
Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FUJIFILM Healthcare Americas Corporation
FDA (openFDA device enforcement)
Reported Mar 26, 2025
Dried Longan Pulp- Made in China, 8oz(227g), GROWLAND INC. rear panel- Organic Planted, Store in cool and dry place,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Growland Inc.
FDA (openFDA food enforcement)
Reported Mar 26, 2025
Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oridion Medical 1987 Ltd.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2025
BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2025
Good & Gather Cut Green Beans. Net Wt. 14.5 oz (411g). UPC 0 85239-11628 9. Dist. By Target Corporation, Minneapolis,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Foods, Inc.
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2025
1.) Market Pantry Soup & Oyster Crackers, NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shearer's Foods, LLC
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Product Name: Pump, Blood,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectrum Medical Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2025
Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Mar 19, 2025
Black Beans, Dried, net wt. 16 OZ (1 LB) 454g, packaged in plastic bag. Packaged in the U.S. UPC 0 70552 70412 1.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Trinidad Benham Corp.
FDA (openFDA food enforcement)
Reported Mar 19, 2025
Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TruAbutment Inc.
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Mar 12, 2025
Access Erythropoietin (EPO), Catalog Number - A16364 a glycoprotein (~30,400 Daltons) produced primarily by the kidney,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, 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.