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.

48701–48725 of 82369

HighFDA (Devices)·Z-1758-2017·2017-04-19
ConMed Recalls Hyfrecator 2000 Accessory Packages with Non-Sterile Sheaths
ConMed is recalling Hyfrecator 2000 accessory packages because they contained non-sterile handpiece sheaths labeled as sterile.
Product
Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons , 220 VOLTS AC, REF/Catalog Number 7-900-220, Rx Only, There is no problem with the Hyfrecator 2000 Electrosurgical Units…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1796-2017·2017-04-19
Windstone Medical Packaging Recalls Plastic Packs with Compromised Sterile Eye Pads
Windstone Medical Packaging is recalling 376 plastic kits containing Medtronic Curity Eye Pads because the sterile packaging may be compromised.
Product
Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1938-2017·2017-04-19
Dolcetta Artisan Sweets Recalls Milk Chocolate Almond Hearts for Undeclared Soy
Dolcetta Artisan Sweets is recalling 30 boxes of Milk Chocolate Almond Hearts due to undeclared soy lecithin. The product was distributed in Oregon and Washington.
Product
Milk Chocolate Almond Heart contains solid milk chocolate with almonds, 110g (4 oz), the product is packaged in a clear plastic box.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1783-2017·2017-04-19
Windstone Medical Packaging Recalls Cataract Kits Due to Sterility Concerns
Windstone Medical Packaging is recalling 4,065 cataract kits because the sterile packaging of the included eye pads may be compromised.
Product
Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1933-2017·2017-04-19
Dolcetta Espresso Caramels Recalled for Undeclared Soy and Milk Allergens
Dolcetta Artisan Sweets is recalling 98 boxes of Espresso Caramels sold in Oregon and Washington due to undeclared soy lecithin.
Product
Espresso Caramels are caramels flavored with expresso, 3.9 oz (110g), individually wrapped in cellophane and then wrapped in a paper box.
Category
Food
Distribution
2 states
HighFDA (Food)·F-1929-2017·2017-04-19
Dolcetta Artisan Sweets Recalls Dark Chocolate Pretzel Bars for Allergens
Dolcetta Artisan Sweets is recalling Dark Chocolate Pretzel Bars because they contain undeclared soy lecithin and wheat.
Product
Dark Chocolate Pretzel Bar contains dark chocolate and pretzels, 1.2 oz (33g), product wrapped in metal foil and then wrapped in paper box.
Category
Food
Distribution
2 states
HighFDA (Food)·F-1946-2017·2017-04-19
Dolcetta Artisan Sweets Recalls Salty Caramels Due to Undeclared Soy and Milk
Dolcetta Artisan Sweets is recalling 80 boxes of Salty Caramels distributed in Oregon and Washington due to undeclared soy lecithin.
Product
Salty Caramels are chewy caramels that are salty, 3.9 oz (110g), individually wrapped in cellophane and then wrapped in a paper box. The label declared "***Salty Caramels *** Cane sugar, cream, butter, golden syrup, sea salt, bourbon vanilla bean***".
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1816-2017·2017-04-19
Hill-Rom TotalCare Bed Systems Recalled for Alarm Malfunction
Hill-Rom is recalling TotalCare Bed Systems because the exit alarm may fail if armed for over 72 hours without triggering.
Product
TotalCare Bed Systems, Model Numbers P1900, PR1900, and U1900 with 3-Level Patient Position Monitoring and Scale Upgrade Kits, Model Numbers P1947A and P1948A).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1924-2017·2017-04-19
Dolcetta Artisan Sweets Recalls Assorted Bonbons for Undeclared Soy Lecithin
Dolcetta Artisan Sweets is recalling Assorted Bonbons because they contain undeclared soy lecithin. The product was distributed in Oregon and Washington.
Product
Assorted Bonbons are molded chocolates with ganache fillings in assorted flavors, No package weight. Product packaged in a black plastic tray and then tray is placed in a paper box with clear plastic lid.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1772-2017·2017-04-19
Draeger Medical Systems Recalls Delta Patient Monitors Due to Low Oxygen Alarm Failure
Draeger Medical Systems is recalling Delta patient monitors used with Scio gas modules because the low oxygen alarm may fail to sound when oxygen levels drop below the set limit.
Product
Delta, Catalog Number: MS18597 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Product Usage: The devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians, Nurses…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1800-2017·2017-04-19
Windstone Medical Vitrectomy Packs Recalled for Sterile Packaging Compromise
Windstone Medical Packaging is recalling 100 Vitrectomy Packs because the sterile packaging of the included eye pads may be compromised.
Product
Vitrectomy Pack, part number AMS4952 Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1934-2017·2017-04-19
Dolcetta Artisan Sweets Recalls Hazelnut Truffles Due to Undeclared Soy Lecithin
Dolcetta Artisan Sweets is recalling 180 boxes of Hazelnut Truffles distributed in Oregon and Washington because the product contains undeclared soy lecithin.
Product
Hazelnut Truffles are dark chocolate with hazelnut ganache, 3.9 oz (110g), individually wrapped in clear cellophane and then wrapped in a paper box.
Category
Food
Distribution
2 states
HighFDA (Food)·F-1941-2017·2017-04-19
Dolcetta Peanut Crisp Truffles Recalled for Undeclared Soy Lecithin
Dolcetta Artisan Sweets is recalling Peanut Crisp Truffles because the product contains undeclared soy lecithin, a potential allergen.
Product
Peanut Crisp Truffles are milk chocolate with peanut butter truffles, 3.9 oz (110g), individually wrapped in clear cellophane and then wrapped in a paper box. The label declared "***Peanut Crisp Truffles***49% milk chocolate, peanut butter, feuilletine (wheat), cocoa powder…
Category
Food
Distribution
2 states
HighFDA (Food)·F-1940-2017·2017-04-19
Dolcetta Artisan Sweets Recalls Milk Chocolate Pretzel Bars for Undeclared Allergens
Dolcetta Artisan Sweets is recalling 400 Milk Chocolate Pretzel Bars distributed in Oregon and Washington due to undeclared soy lecithin and wheat.
Product
Milk Chocolate Pretzel Bar, net wt. 1.2 oz (33g), product wrapped in metal foil and then wrapped in paper box. The label declared: "***Milk Chocolate Pretzel Bar*** 49% milk chocolate, pretzels, butter, sea salt, baking soda***".
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1778-2017·2017-04-19
Merge Hemo software recall for incorrect FFR results display
Merge Healthcare is recalling Merge Hemo software versions 9.10.0 through 9.40.0 because they may display incorrect Fractional Flow Reserve values during cardiac catheterization.
Product
Merge Hemo software. The firm name on the labeling is Merge Healthcare, Hartland, WI. Merge Hemo monitors, measures, and records physiologic data from a human patient undergoing a cardiac catheterization procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1791-2017·2017-04-19
Windstone Medical Eye Pack Recall Due to Sterile Packaging Compromise
Windstone Medical Packaging is recalling 1,330 Eye Packs because the sterile packaging of the included eye pads may be compromised.
Product
Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1788-2017·2017-04-19
Windstone Medical Recalls Dr. Wischmeier Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 1,170 Dr. Wischmeier Packs because the sterile packaging of the included eye pads may be compromised.
Product
Dr. Wischmeier Pack, part numbers: AMS3509 and AMS3509(A Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1801-2017·2017-04-19
BioMerieux Recalls VIDAS Estradiol II Assay Due to Fulvestrant Cross-Reactivity
BioMerieux SA is recalling VIDAS Estradiol II kits because Fulvestrant treatment can cause falsely elevated estradiol results.
Product
VIDAS Estradiol II, Ref 30431-01, 60 tests The VIDAS Estradiol II (E2 II) assay is intended for use on the instruments of the VIDAS family (VITEK ImmunoDiagnostic Assay System) as an automated quantitative enzyme-linked fluorescent immunoassay (ELFA) to the determination of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1922-2017·2017-04-19
Gerber Pasta Pick-Ups Cheese Ravioli Recalled for Missing Egg Allergen Label
Gerber is recalling Pasta Pick-Ups Cheese Ravioli because the egg allergen is missing from the 'Contains' statement on the packaging.
Product
Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Drained Wt 3 oz (85g) UPC 01500000907-6 , Truncated - written on package as: UPC 159070
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1787-2017·2017-04-19
Windstone Medical Recalls Dicken Eye Packs Due to Sterility Concerns
Windstone Medical Packaging is recalling 172 Dicken Eye Packs because the sterile packaging of the eye pads may be compromised.
Product
Dicken Eye Pack, part number CPA-3202-2. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1931-2017·2017-04-19
Dolcetta Dark Chocolate Toffee Santa Recalled for Undeclared Soy Lecithin
Dolcetta Artisan Sweets is recalling 20 boxes of Dark Chocolate Toffee Santa because the product contains undeclared soy lecithin.
Product
Dark Chocolate Toffee Santa, dark chocolate with bits of toffee, 150g (5.3 oz), the product is packaged in a clear plastic box.
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1794-2017·2017-04-19
Windstone Medical Ophthalmic Packs Recalled for Sterile Packaging Compromise
Windstone Medical Packaging is recalling 169 ophthalmic packs containing Medtronic Curity Eye Pads because the sterile packaging may be compromised.
Product
Ophthalmic Pack, Part number WAL1107(A and WAL1190 Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1799-2017·2017-04-19
Windstone Medical Vitrectomy Kits Recalled for Sterile Packaging Compromise
Windstone Medical Packaging is recalling Vitrectomy Kits because the sterile packaging of the included Medtronic Curity Eye Pad may be compromised.
Product
Vitrectomy Kit, part number CMP1016(A. Product packaged in a convenient manner for use in a general clinical procedure
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1756-2017·2017-04-19
ConMed Recalls Sterile Handpiece Sheaths Packaged in Error
ConMed is recalling sterile handpiece sheaths that were packaged in error with non-sterile units. The mislabeling could lead to the use of non-sterile sheaths.
Product
Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 100 VOLTS AC, REF/Catalog Number 7-900-100, Rx Only. There is no problem with the Hyfrecator 2000 Electrosurgical Unit. -- ASSEMBLED…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1944-2017·2017-04-19
Dolcetta Salted Caramel Bonbons Recalled for Undeclared Soy Lecithin
Dolcetta Artisan Sweets is recalling Salted Caramel Bonbons because the product contains undeclared soy lecithin, a major food allergen.
Product
Salted Caramel Bonbons are molded chocolate shells filled with salted caramel ganache, 1.7 oz (48g), the product is placed into a clear plastic box package and then put into a paper box package. The label declared "***Salted Caramel Bonbons *** Shell: 60% dark chocolate, 32%…
Category
Food
Distribution
2 states