State

Washington product recalls

73,219 recalls have nationwide distribution and so reach Washington. 8,460 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total: 8,460
Critical: 868
Severe: 2,008
Most recent: 2026-09-30

Of the 8,460 recalls naming Washington we have scored against our rubric, 868 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,008 (24%) are Severe.

Which agencies issued them

These figures cover only the 8,460 recalls whose distribution notice names Washington specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15776–15800 of 81679

SevereFDA (Devices)·Z-2368-2023·2023-08-23
Dialysis Catheter Recalled Due to Excessive Lubricant Causing Center Lumen Obstruction
Covidien is recalling MAHURKAR dialysis catheters due to excessive silicone-based lubricant coating the center lumen tip, which may cause partial or complete obstruction, delaying treatment or causing thrombosis.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, IC Tray REF: 8888101002HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2375-2023·2023-08-23
Dialysis catheter recalled due to excessive lubricant causing obstruction
Covidien's MAHURKAR dialysis catheter is recalled because excessive silicone lubricant can block the center lumen, preventing or reducing blood flow during dialysis. This Class I recall affects 271 units and carries risk of treatment delays, hemolysis, and blood clots.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, PASS Tray REF: 8888103004HP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2414-2023·2023-08-23
FreeStyle Libre 2 Readers may fail to activate new sensors
FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.
Product
FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1405-2023·2023-08-23
Dilettante Dark Ephemere Bulk Truffles Milk Allergen Mislabeling
Dilettante Mocha Cafe Dark Ephemere Bulk Truffles' display placard lists milk in ingredients but declares only 'Contains: Dairy,' not 'Contains: Milk.' Bulk boxes have correct allergen labeling.
Product
Dilettante Mocha Cafe brand Dark Ephemere Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk, cream, and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes…
Category
Food
Distribution
1 state
HighFDA (Food)·F-1410-2023·2023-08-23
Dilettante Mocha Cafe Amaretto Bulk Truffle Allergen Labeling Error
Dilettante Chocolates is recalling Mocha Cafe brand Amaretto Bulk Truffle chocolate sold from retail display cases due to incomplete allergen declaration on the display placard.
Product
Dilettante Mocha Cafe brand Amaretto Bulk Truffle, perishable, sold individual pieces out of retail display cases. The display placard declares milk chocolate and almond extract in the ingredients statement, but the Contains statement declares "Contains: Dairy, Nuts". Bulk…
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-2413-2023·2023-08-23
HF Resection Electrodes Recalled for Wire Breakage and Patient Fragment Hazard
Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.
Product
HF Resection Electrodes - HF resection electrodes are part of a resectoscope system for endoscopic diagnosis and treatment in urological or gynecological applications. 64 Models: 1) A22201C 2) A22201D 3) A22202C 4) A22203C 5) A22205C 6) A22205D 7) A22206C 8)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1408-2023·2023-08-23
Dilettante Mocha Cafe Champagne Truffles recalled for milk allergen labeling discrepancy
Dilettante Mocha Cafe Champagne Bulk Truffles are being recalled due to milk allergen labeling errors on display case placards in Washington. The allergen declaration does not adequately reflect milk content.
Product
Dilettante Mocha Cafe brand Champagne Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores…
Category
Food
Distribution
1 state
HighFDA (Drugs)·D-1084-2023·2023-08-23
Toothpaste Label Mix-Up: Wrong Tube Labels in Strawberry Cartons
Hello wild strawberry fluoride toothpaste cartons contain tubes incorrectly labeled as hello fresh watermelon fluoride free toothpaste. 182,046 units affected nationwide.
Product
hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1406-2023·2023-08-23
Dilettante Mocha Cafe Truffles recalled for incomplete milk allergen labeling
Dilettante Chocolates Inc is recalling Mocha Cafe brand Light Ephemere Bulk Truffles sold from retail display cases in Washington due to incomplete allergen labeling on the display placard.
Product
Dilettante Mocha Cafe brand Light Ephemere Bulk Truffles, perishable, sold in individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes…
Category
Food
Distribution
1 state
HighFDA (Food)·F-1416-2023·2023-08-23
Dilettante Mocha Cafe Toffee Recalled for Incomplete Allergen Labeling
Dilettante Chocolates recalls Rheingold White Bulk Toffee sold at Washington retail locations due to display placard with incomplete allergen declarations. The placard did not fully identify milk and specific nut allergens present in the product.
Product
Dilettante Mocha Cafe brand Rheingold White Bulk Toffee, perishable, sold individual pieces out of retail display cases. The display placard declares milk, pecans and hazelnuts in the first Contains statement, and the 2nd Contains statement declares "Contains: Dairy, Nuts".…
Category
Food
Distribution
1 state
HighFDA (Food)·F-1414-2023·2023-08-23
Dilettante Mocha Cafe Rheingold Dark Bulk Toffees recalled for incomplete allergen labeling
Dilettante Chocolates Inc recalled Rheingold Dark Bulk Toffees distributed to Washington retail locations because the display placard's allergen declaration is incomplete. The placard states "Contains Dairy, Nuts" but does not specify the milk, almonds, and pecans present in the product.
Product
Dilettante Mocha Cafe brand Rheingold Dark Bulk Toffees, perishable, sold individual pieces out of retail display cases. The display placard declares butter, pecans, and almonds in the ingredients statement, but the Contains statement declares "Contains: Dairy, Nuts". Bulk…
Category
Food
Distribution
1 state
HighNHTSA·23V592000·2023-08-23
Bentley Recalls 2017-2023 Bentayga Vehicles for Fuel Leak Fire Risk
Bentley is recalling 2017-2023 Bentayga vehicles because fuel supply module wiring can overheat, melt a flange, and cause a fuel leak that increases fire risk.
Product
BENTLEY — BENTLEY BENTAYGA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2401-2023·2023-08-23
UroPass Ureteral Access Sheaths Recalled for Dilator Tip Breakage
Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.
Product
UroPass Ureteral Access Sheaths, 5 pieces/box
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2405-2023·2023-08-23
Hip Screw Labeled as Wrong Size: 30mm Screws Mislabeled as 25mm
Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.
Product
CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2407-2023·2023-08-23
Centurion FMS Pak Recalled Due to Patient Injury Risk from Plastic Debris
Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.
Product
Centurion FMS Pak
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V593000·2023-08-23
Volkswagen Recalls 2024 Atlas Cross Sport for Engine Bearing Defect
Volkswagen is recalling 2024 Atlas and Atlas Cross Sport vehicles because engine bearings may fail, causing engine stalls and increasing the risk of crashes and fires.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1411-2023·2023-08-23
Dilettante Dark Ginger Bulk Truffles Recalled for Inadequate Milk Allergen Labeling
Dilettante Chocolates recalled Dark Ginger Bulk Truffles from Washington retail stores because the display placard's allergen declaration fails to clearly identify milk. The product boxes have the correct label.
Product
Dilettante Mocha Cafe brand Dark Ginger Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail…
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1419-2023·2023-08-23
Dilettante Mocha Cafe Caramels Display Placard Allergen Labeling Inconsistency
Dilettante Chocolates Inc is recalling caramels sold from display cases because the display placard's allergen statement is incomplete. The placard lists only 'Contains: Dairy' despite cream and butter being shown in the ingredients list.
Product
Dilettante Mocha Cafe brand Himalayan Pink Salt Bulk Caramels, perishable, sold individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes…
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1418-2023·2023-08-23
Dilettante Mocha Cafe Espresso Bulk Caramels Recalled for Labeling Discrepancy
Dilettante Chocolates is recalling Mocha Cafe Espresso Bulk Caramels sold at its Washington retail locations due to a display placard allergen declaration that states 'Contains: Dairy' instead of 'Contains: Milk,' though milk is listed in the ingredients.
Product
Dilettante Mocha Cafe brand Espresso Bulk Caramels, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores…
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1407-2023·2023-08-23
Dilettante Mocha Cafe Dark Raspberry Truffles display placard mislabeled for allergens
Dilettante Chocolates recalls Mocha Cafe Dark Raspberry Bulk Truffles sold at retail stores in Washington due to incomplete allergen labeling on display placards. The product contains dairy but the allergen declaration is incomplete.
Product
Dilettante Mocha Cafe brand Dark Raspberry Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent…
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-2412-2023·2023-08-23
Medtronic ventricular catheter system recalled due to incorrect labeling expiration date
Medtronic is recalling 44 units of the Duet External Drainage and Monitoring system because the product labels contain an incorrect expiration date. The affected lot (226632942) was distributed nationwide.
Product
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1417-2023·2023-08-23
Dilettante Mocha Cafe Sriracha Bulk Caramels Recalled for Labeling Inconsistency
Dilettante Chocolates is recalling Mocha Cafe brand Sriracha Bulk Caramels sold at Washington retail locations due to inconsistent dairy allergen labeling on display case placards versus case boxes.
Product
Dilettante Mocha Cafe brand Sriracha Bulk Caramels, perishable, sold individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to…
Category
Food
Distribution
1 state
ModerateFDA (Food)·F-1413-2023·2023-08-23
Dilettante Espresso Truffles Recall: Incomplete Allergen Labeling on Display
Dilettante Chocolates recalls Mocha Cafe Espresso Bulk Truffles sold at Washington retail locations. The retail display placard's allergen statement declares 'Contains: Dairy' instead of the required 'Contains: Milk.'
Product
Dilettante Mocha Cafe brand Espresso Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores…
Category
Food
Distribution
1 state
ModerateFDA (Drugs)·D-1086-2023·2023-08-23
Tobramycin Ophthalmic Solution recalled for failed quality specifications
Alembic Pharmaceuticals is recalling 82,400 bottles of Tobramycin Ophthalmic Solution nationwide because the product failed to meet impurities and degradation specifications.
Product
TOBRAMYCIN OPHTHALMIC SOLUTION — TOBRAMYCIN OPHTHALMIC SOLUTION (TOBRAMYCIN OPHTHALMIC SOLUTION)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1412-2023·2023-08-23
Dilettante Mocha Cafe Praline Truffles Recalled for Imprecise Allergen Labeling
Dilettante Chocolates Inc recalled Dilettante Mocha Cafe brand Praline Bulk Truffles because display placards use general allergen categories (Dairy, Nuts) instead of specific allergen sources (Milk, Almond, Pecan).
Product
Dilettante Mocha Cafe brand Praline Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk, pecans, and almonds in the ingredients statement, but the Contains statement declares "Contains: Dairy, Nuts". Bulk truffle…
Category
Food
Distribution
1 state