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.
4,362 stored notices name Washington, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Washington too — those are in the archive.
Reported Jun 3, 2020
Optilite Optilite Rheumatoid Factor Kit, Ref: LK151.OPT.A, IVD, Rx Only, UDI: 05051700020015 (kit ea. containing four…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
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
TorFlex Transseptal Guiding Sheath ; Model numbers: TF8-32-63-45, TF8-32-63-55, TF8-32-63-90, TF8-32-63-135,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baylis Medical Company Inc.
1 more product 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)
Reported May 20, 2020
Analyte specific reagent. REF/UDI: 641408/641408-4012-1-1 (US); 641417/641417-1157-1-01 (OUS); 641399/641399-4012-1-01…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported May 20, 2020
The product is twisted bread and packaged in a flexible plastic bag with a yellow Kwik-Lok seal. The label is read in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Essential Baking Company, The
FDA (openFDA food enforcement)
Reported May 20, 2020
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
Inpeco FlexLab, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: FLX-208-00, FLX-208-10 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inpeco S.A.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported May 20, 2020
Ra Medical Systems DABRA Catheter 5F (1.5mm), REF: 1222-5000-01, LOT: 18-090400-094, USE BY: 2019-09-24, MFR DATE:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ra Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 20, 2020
Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Magstim Company Limited
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Glaxosmithkline Consumer Healthcare Holdings
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 13, 2020
Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported May 13, 2020
REF: AH7117 111" 10 Drop Admin Set w/2 Inj Sites, Rotating Luer, Sterile R, For Veterinary Use Only, (01) 1 0887709…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Inpeco FlexLab Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inpeco S.A.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
da Vinci Xi Surgical System, IS4000 - Product Usage: The da Vinci Xi surgical system (IS4000) is made of three main…
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 May 13, 2020
daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx Only, Sterile EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Visualase Cooled Laser Applicator System Tubing Set kits Product numbers: VCLAS 9735559, 3mm tip/1.65mm catheter VCLAS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
ICU Medical Cogent Hemodynamic Monitoring System, Cogent Item Number 58400-000, UDI: (01)00840619079499
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, 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.