The Recall Desk

State

Washington product recalls

73,833 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,536
Critical
865
Severe
2,405
Most recent
2026-11-04

Of the 8,536 recalls naming Washington we have scored against our rubric, 865 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50326–50350 of 82369

  • SevereFDA (Devices)·Z-0887-2017·2016-12-28

    Amendia Recalls Black Widow Spinal Screws Due to Mating Feature Defect

    Amendia, Inc. is recalling 96 units of Black Widow 6.6mm spinal screws due to a design defect in the mating feature between the plate and screw.

    Product
    Black Widow 6.6mm x 20mm Screw, Part Number TBS020; Black Widow 6.6mm x 25mm Screw, Part Number TBS025; Black Widow 6.6mm x 30mm Screw, Part Number TBS030 The Black Widow Buttress Plates and Screws are designed for preventing migration or expulsion of allograft or autograft in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0889-2017·2016-12-28

    Medtronic Recalls Clearify Visualization Systems Due to Sterility Compromise

    Medtronic is recalling 1,293,169 Clearify Visualization Systems because a breach of the sterile barrier compromises product sterility.

    Product
    Covidien Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during endoscopic and laparoscopic procedures to prevent fogging of the scope as well as clean the scope lens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0878-2017·2016-12-28

    Merge OrthoCase software recall due to measurement errors

    Merge Healthcare is recalling OrthoCase software because measurements change after saving, potentially causing patient injury or delayed diagnosis.

    Product
    Merge OrthoCase software. The firm name on the label is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    15 states
  • SevereFDA (Drugs)·D-0217-2017·2016-12-28

    Novo Nordisk Recalls GlucaGen HypoKits Due to Detached Needles

    Novo Nordisk is recalling 71,215 GlucaGen HypoKits because the syringe needles may be detached. The recall covers lots expiring in September 2017.

    Product
    GlucaGen HypoKit (glucagon [rDNA origin] for injection), 1 mg per vial, Single use only, Rx Only, Manufactured by: Novo Nordisk A/S 2880 Bagsvaerd, Denmark, NDC 0169-7065-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0212-2017·2016-12-28

    Virtus Recalls Hyoscyamine Sulfate Tablets Due to Content Uniformity Failures

    Virtus Pharmaceuticals is recalling Hyoscyamine Sulfate sublingual tablets because they failed content uniformity specifications, resulting in tablets that are either superpotent or subpotent.

    Product
    Hyoscyamine Sulfate, Sublingual Tablets, 0.125 mg, 100-count bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-309-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0892-2017·2016-12-28

    Medtronic Recalls PowerCross .018 OTW PTA Dilatation Catheters

    Medtronic is recalling 315 units of the PowerCross .018 OTW PTA Dilatation Catheter due to a manufacturing defect causing the balloon to fail to inflate or deflate properly.

    Product
    ev3, PowerCross .018 OTW PTA Dilatation Catheter, Sterile EO. The PowerCross .018 OTW PTA Dilatation Catheter is intended to dilate stenoses in the iliac, femoral, ilio-femoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of…
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-0944-2017·2016-12-28

    Ariels OM Grown Granola Recalled for Wheat Seed Contamination

    Hummingbird Wholesale is recalling Ariels OM Grown Granola because it was contaminated with wheat seed. The product was distributed in California, Oregon, and Washington.

    Product
    Ariels OM Grown Granola. Product number GR200, net wt. 5 lb., packaged in bulk bag inside plastic bucket. Product number GR201, net wt.15 lb., packaged in bulk bag inside plastic bucket. Product number BAG-GR200, net wt. 8 oz., packaged in cellophane bag with cardstock…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0900-2017·2016-12-28

    Exactech Recalls Equinoxe Reverse Shoulder Screw Kits Due to Disengaged Heads

    Exactech, Inc. is recalling 2,278 Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kits because disengaged screw heads may not be retained in the screwdriver.

    Product
    Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0830-2017·2016-12-28

    Northern Fish Products Recalls Smoked Fish for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy.

    Product
    NORTHERN CLASSICS NATURAL SMOKED STEELHEAD*** Product is packaged in bulk 5lb case. Product is vacuum packaged catch weight.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0811-2017·2016-12-28

    Brownwood Farms Cherry BBQ Sauce Recalled for Undeclared Soy

    Brownwood Farms is recalling Cherry BBQ Sauce because it contains soy ingredients that are not declared on the label.

    Product
    Brownwood Farms Cherry BBQ Sauce. 21oz glass bottles, 1 gallon, 5 gallon. Private labels: Arbor Day Farm (Cherry BBQ Sauce). Bowers Harbor Vineyard (Cherry BBQ Sauce 12oz). Benjamin Twiggs (Northwoods Cherry BBQ Sauce 16oz). Crossroads. Friske Orchards. Kimmel Orchard &…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V953000·2016-12-28

    RAM ProMaster City Recalled for Side Air Bag Defect

    Chrysler is recalling one 2017 RAM ProMaster City because its side curtain air bags may not inflate properly in a crash.

    Product
    RAM — RAM PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0756-2017·2016-12-28

    Real Fudge Peanut Butter Fudge Recalled for Undeclared Blue #1

    Real Fudge is recalling Peanut Butter Fudge because it contains undeclared Blue #1, a food dye not listed on the label.

    Product
    Peanut Butter Fudge, brand Real Fudge. Product is sold in clear plastic deli container in 8, 12, and 16 oz.
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·16V936000·2016-12-28

    Maserati Recalls 2017 Levante S for Engine Software Defect

    Maserati is recalling 2017 Levante S vehicles because engine software may cause the transmission to shift to neutral or the engine to shut down at low speeds.

    Product
    MASERATI — MASERATI LEVANTE S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0822-2017·2016-12-28

    Northern Fish Products Recalls Smoked Salmon for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy. Hot jerky salmon and jerky salmon are excluded.

    Product
    "***PREMIUM SMOKED SALMON***CRACKED PEPPER*** NET WT: 4OZ***Packaged 5 lbs case 20/4oz vacuum packages/case. Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee. UPC 7 02772 00560 2.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0827-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Sweet & Spicy Style Atlantic Salmon, Product of USA Packed By Northern Fish Products***" Packaged in bulk 5lb case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0828-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Kippered Salmon Tips Product of USA Packed By Northern Fish Products***" Packaged in bulk 5lb case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0885-2017·2016-12-28

    Siemens IMMULITE 2000 PSA Assay Recalled for Hook Effect Performance Issues

    Siemens Healthcare Diagnostics is recalling IMMULITE 2000 PSA assays because they do not meet the High-dose Hook Effect expectations stated in the Instructions for Use.

    Product
    IMMULITE 2000/IMMULITE 2000 XPi Systems Prostate-Specific Antigen (PSA) Assay, REF/Catalog Number L2KPTS2, SMN 10706281 and REF/Catalog Number L2KPTS6, SMN 10706282 (US); REF/Catalog Number L2KPS2, SMN 10380986 and REF/Catalog Number L2KPS6, SMN 10380996 (OUS); IVD --- Origin…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0775-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Detachment Risk

    AngioDynamics is recalling 996 boxes of Stiffened Micro-Introducer Kits because the rotating luer on the included sheath/dilator components may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO B PG, Item Number H787065970515, Catalog No.REF 06597051, 2) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO S PG, Item Number H787065970535, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0829-2017·2016-12-28

    Northern Fish Products Recalls Smoked Fish Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because they contain undeclared soy.

    Product
    Brown Sugar Style Smoked Black Cod Black Cod, **Product of USA Packed By Northern Fish Products***" Packaged in bulk 5lb case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0777-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Detachment Risk

    AngioDynamics is recalling 7 boxes of Stiffened Micro-Introducer Kits because the rotating luer on the included sheath/dilator components may detach from the hub during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T NON-ECHO B PG, Item Number H787065970685, Catalog No.REF 06597068, 2) 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T NON-ECHO S PG, Item Number H787065970705…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0825-2017·2016-12-28

    Northern Fish Products Recalls Hot Smoked Salmon Due to Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout because the products contain undeclared soy.

    Product
    PREMIUM SMOKED SALMON***CAJUN***NET WT: 4OZ***Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee. UPC 7 02772 00562 6.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0823-2017·2016-12-28

    Northern Fish Products Recalls Smoked Salmon for Undeclared Soy

    Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout due to undeclared soy.

    Product
    WILD CATCH PREMIUM SMOKED SALMON***NATURAL***NET WT: 4OZ*** UPC 7 02772 00559 6. Cardboard type label is folded over and affixed to the top of the package. Sell by date is marked on the label by the consignee.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0773-2017·2016-12-28

    AngioDynamics Recalls Stiffened Micro-Introducer Kits Due to Component Defect

    AngioDynamics is recalling 80 boxes of Stiffened Micro-Introducer Kits because a component may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T ECHO B PG, Item Number H787065970465, Catalog No.REF 06597046, 2) 4 F Stiffened Micro-Introducer Kit, 45CM SS/T ECHO S PG, Item Number H787065970485, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide