Recalls distributed in Washington
These notices name Washington 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.
4,412 stored notices name Washington, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Washington too — those are in the archive.
In the agency's Nov 11, 2026 enforcement report
Generic Name: Edwards Commander M Delivery System Generic Name: Edwards Commander M Delivery System Model/Catalog…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (weekly enforcement report)
In the agency's Nov 11, 2026 enforcement report
Nextseq 550Dx Instrument REF: 20005715, FOR IN VITRO DIAGNOSTIC USE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
2 more products in this recall
FDA (weekly enforcement report)
In the agency's Nov 11, 2026 enforcement report
EVOS 3.5MM LATERAL PROXIMAL TIBIA PLATE 6 HOLE LEFT 91MM REF72463106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (weekly enforcement report)
In the agency's Nov 11, 2026 enforcement report
Tandem Mobi Insulin Pump, Models: 1004004, 1010750, 1012676, 1012719, 1013655, 1013656, 1013501, 1013700, 1014081,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tandem Diabetes Care, Inc.
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
EDEN BROTHERS Broccoli Seeds - Calabrese. Sold in packets, Net Wt. 1oz pouches, UPC SVBRO111 -qb2 & 1 Pound pouches UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eden Brothers
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
Precision Pointer Electromagnetic (8000-050-001)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Leibinger GmbH & Co. KG
FDA (weekly enforcement report)
In the agency's Nov 4, 2026 enforcement report
Orthoscan VERSA Accessory Cart, REF: 1000-0021 and Versa Mini C-Arm System, REF: 1000-0020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm-Orthoscan Inc.
FDA (weekly enforcement report)
Reported Oct 28, 2026Updated Nov 2, 2026
PNE Lead Implant Kit REF: 1701
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Axonics, Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
B Braun SAFSITE Injection Site, RV1000NC SAFSITE VALVE W/O EXTRA CAP. Catalog Number: 415068.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Raw In-Shell Peanuts; packed in a clear plastic 1lb, 5lb, 50lb unit sizes. Raw Spanish Peanuts; sold by weight (bulk)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.El Ruisenor De Mexico, Inc.
12 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Evexias Health Solutions Amino Ultra, 90-capsules, dietary supplement in white plastic bottles with blue/green/white…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Evexias Health Solution
FDA (openFDA food enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
GEARHARTS FINE CHOCOLATES Net Wt. 4oz UPC 8 98111 00205 7; Net Wt. 8oz UPC 8 98111 00206; Gearharts Fine Chocolates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gearharts Fine Chocolates, Inc.
FDA (openFDA food enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Medtronic NDI Passive Spheres REF: 8801075, Sterile EO, 5/Tray 12 Pk., Rxonly
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 Oct 28, 2026Updated Nov 2, 2026
Great Value Fruit Cocktail in Fruit Juice from Concentrate NET WT 15 OZ (425g) DISTRIBUTED BY: Walmart Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Coast Producers
FDA (openFDA food enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Philips Lumify Diagnostic Ultrasound System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Ultrasound, LLC
FDA (openFDA device enforcement)
Reported Oct 28, 2026Updated Nov 2, 2026
Sempio Yellow Peach; Product of Korea; NET WT. 14.10 oz. UPC: 8801005320825
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sempio Food Services, Inc.
FDA (openFDA food enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
DxU 840m Iris, REF: C76947; DxU 850m Iris, REF: C49513
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Nov 2, 2026
Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Williams Cystoscopic Injection Needles, used for cystoscopic injection into the urethra, bladder neck, and bladder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Incorporated
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
Power F2 Powered Fastening System, Power F2, Item No. 0567093 used with Power X2 Stretchers, Power X2, Item No. 0015816…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
HemoslL AcuStar HIT-lgG(PF-4). Part Number: 0009802028. in vitro diagnostic (OUS only)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Instrumentation Laboratory
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
JenaValve Trilogy Delivery Catheter, Size 27MM REF: TRILOGY-DC-L
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jenavalve Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
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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.