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.

49751–49775 of 82369

  • ModerateFDA (Devices)·Z-1117-2017·2017-02-08

    Ortho-Clinical VITROS Na+ Slides Recalled for Potential Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Na+ Slides because they may produce biased results if stored on the analyzer for 10 days after minimum warm-up.

    Product
    VITROS Na+ Slides, (UPN 10758750004812) For in vitro diagnostic use only. VITROS Na+ Slides quantitatively measure sodium (Na+) concentration in serum, plasma, and urine using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1118-2017·2017-02-08

    Siemens Mammomat Inspiration Mammography Systems Recalled for Software Error

    Siemens Medical Solutions USA is recalling 55 Mammomat Inspiration digital x-ray mammography systems due to a software error.

    Product
    Mammomat Inspiration full, field digital,system,x-ray,mammographic Product Usage: The Mammomat Inspiration system is intended for mammography exams, screening, diagnosis, and stereotactic biopsies under the supervision of medical professionals. Mammographic images can be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1427-2017·2017-02-08

    Roland Manzanilla Olives Stuffed With Anchovies Recalled for Microorganisms

    Roland Foods is recalling Manzanilla Olives Stuffed With Anchovies because FDA sampling found non-pathogenic Gram Positive Rods.

    Product
    Roland MANZANILLA OLIVES STUFFED WITH ANCHOVIES, DR. WT. 3 OZ. (85g), UPC Code: 41224714021 and Case UPC Code: 10041224714028, Item # 71402, PRODUCT OF SPAIN
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17732·2017-02-07

    Sony Expands Recall of VAIO Laptop Battery Packs for Fire Hazards

    Sony is expanding a recall of Panasonic lithium-ion battery packs used in VAIO laptops due to overheating risks that can cause burns and fires.

    Product
    Panasonic battery packs used in Sony Electronics laptop computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V074000·2017-02-07

    Cruiser RV Recalls 2016-2017 Boss Trailers Due to Furnace Exhaust Defect

    Cruiser RV is recalling 2016-2017 Boss recreational trailers because a vertically-mounted furnace may have exhaust ports at the top, creating an unsafe operating condition.

    Product
    CRUISER RV — CRUISER RV BOSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V070000·2017-02-03

    Volkswagen Recalls 2017 Jetta Vehicles Due to Engine Seizure Risk

    Volkswagen is recalling 2017 Jetta vehicles with 1.4L engines because the engine block may be improperly cast, potentially causing the engine to seize and leading to a loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V072000·2017-02-03

    REV Recalls 2016-2017 Motorhomes Due to Fuel Leak Risk

    REV Recreation Group is recalling 391 Holiday Rambler and Fleetwood motorhomes because a spring shackle bolt may puncture fuel components, creating a fire hazard.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER XE, STORM, VACATIONER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V071000·2017-02-03

    Midwest All-Poly 3000 Series Recalled for Brake Light Switch Defect

    Midwest Fire Equipment is recalling one 2017 All-Poly 3000 Series vehicle because the stop light switch may fail to illuminate brake lights, increasing crash risk.

    Product
    MIDWEST — MIDWEST ALL-POLY 3000 SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17V068000·2017-02-02

    Nissan Recalls 2002 Pathfinder and Infiniti QX4 for Air Bag Defect

    Nissan is recalling 2002 Pathfinder and Infiniti QX4 vehicles because the front passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    INFINITI — INFINITI, NISSAN QX4, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17081·2017-02-02

    Disney Recalls Mickey Mouse Nightlights Due to Fire Hazard

    Walt Disney Parks and Resorts is recalling Happy Holidays! Mickey Mouse Nightlights because liquid can leak onto electrical outlets, posing a fire hazard.

    Product
    Happy Holidays! Mickey Mouse Nightlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V067000·2017-02-02

    BMW Recalls 2011-2012 Models for Rear Driveshaft CV Joint Defect

    BMW is recalling specific 2011-2012 models because the rear driveshaft CV joint may break, causing loss of propulsion and increasing crash risk.

    Product
    BMW — BMW 335I, Z4, 335D, 535I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V066000·2017-02-02

    Jayco Recalls 2017 Seismic Fifth-Wheel Trailers Due to Brake Wiring Defect

    Jayco is recalling 2017 Seismic and Seismic Wave fifth-wheel trailers because improper wiring may prevent the breakaway switch from functioning, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC WAVE, SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1361-2017·2017-02-01

    Earth Balance Vegan Mac and Cheese Recalled for Undeclared Milk

    Boulder Brands is recalling Earth Balance Vegan Mac and Cheese products due to undeclared milk, a major allergen.

    Product
    Earth Balance Vegan White Cheddar flavored Mac and Cheese, 6oz package, Cardboard box/carton, 12 packages per distributed case, Ambient storage.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0923-2017·2017-02-01

    Philips Allura Xper FD10 X-ray System Recalled for Loose Screws

    Philips is recalling one Allura Xper FD10 X-ray system because production errors left screws loose, potentially causing the C-arm to rotate uncontrolled.

    Product
    Allura Xper FD10 722026 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·17V065000·2017-02-01

    Highland Ridge Recalls 2016-2017 Open Range Fifth-Wheels for Axle Defect

    Highland Ridge RV is recalling 2016-2017 Open Range fifth-wheel vehicles because axle hangers may puncture the riser tube, causing axle misalignment and tire failure.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0925-2017·2017-02-01

    Philips Allura Xper FD20/15 C-arm Recall Due to Loose Screws

    Philips is recalling two Allura Xper FD20/15 systems because production errors may cause C-arm screws to loosen, leading to uncontrolled rotation.

    Product
    Allura Xper FD20/15 R8.2 722058 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0924-2017·2017-02-01

    Philips Allura Xper FD20 C-arm Recall Due to Loose Screws

    Philips is recalling two Allura Xper FD20 C-arm systems because production errors left screws loose, posing a risk of uncontrolled rotation.

    Product
    Allura Xper FD20 R8.2 722028 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electrophysiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1099-2017·2017-02-01

    Roche Recalls Accu-Chek Connect App Due to Insulin Dosing Errors

    Roche Diabetes Care is recalling the Accu-Chek Connect app because software defects may cause incorrect insulin bolus recommendations, potentially leading to hypoglycemia.

    Product
    Accu-Chek Connect Diabetes Management App
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1343-2017·2017-02-01

    Stauffer's Animal Crackers Recalled for Potential Milk Contamination

    D. F. Stauffer Biscuit Co. is voluntarily recalling 32 oz. Original Animal Crackers because they may be packaged with cookies containing milk powder.

    Product
    FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716 or LD120716; Stauffer Biscuit Co., York, PA 17403.
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-1362-2017·2017-02-01

    Earth Balance Vegan Mac and Cheese Recalled for Undeclared Milk

    Boulder Brands is recalling Earth Balance Vegan Mac and Cheese products because they contain undeclared milk, a major allergen.

    Product
    Earth Balance Vegan Cheddar flavored Mac and Cheese, 6oz package, Cardboard box/carton, 12 packages per distributed case, Ambient storage.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0922-2017·2017-02-01

    Philips Allura Xper FD20 C-arm Recall for Loose Screws

    Philips is recalling one Allura Xper FD20 unit because production errors left screws loose, which could cause the C-arm to rotate uncontrolled.

    Product
    Allura Xper FD20 722012 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1097-2017·2017-02-01

    Softbank II Transfusion Software Recalled for Potential Incorrect Results

    Soft Computer Consultants is recalling Softbank II software due to a software error that may produce incorrect results in transfusion services.

    Product
    SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare facilities. Used by healthcare personal to document, query, and view the integrated information regarding patients and products. Quality control testing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1077-2017·2017-02-01

    Roche Recalls 30 Cobas b 123 POC Systems for Quality Control Issue

    Roche Diagnostics is recalling 30 cobas b 123 POC systems because a software issue may prevent automatic quality control from running, potentially leading to undetected incorrect test results.

    Product
    Cobas b 123 POC system The cobas b 123 POC system is a fully automated POC system for whole blood in vitro measurement of pH, blood gases (B3G), electrolytes Nat, K+, iCaWt (ISE), hematocrit (THct), metabolites (Glu, Lac), total hemoglobin (tHb), hemoglobin derivatives (O2Hb…
    Category
    Medical Device
    Distribution
    Distributed nationwide