The Recall Desk

State

Washington product recalls

72,986 recalls have nationwide distribution and so reach Washington. 8,456 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,456
Critical
867
Severe
2,006
Most recent
2026-09-09

Of the 8,456 recalls naming Washington we have scored against our rubric, 867 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,006 (24%) are Severe.

These figures cover only the 8,456 recalls whose distribution notice names Washington specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6751–6775 of 81442

  • SevereFDA (Food)·F-0852-2025·2025-06-11

    Fresh & Ready Foods Dark Wheat Sandwich recalled for Listeria contamination risk

    Fresh & Ready Foods is recalling Dark Wheat Sandwiches due to Listeria monocytogenes detected on food contact surfaces in the manufacturing facility.

    Product
    Fresh & Ready Foods Dark Wheat Sandwich, 7oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89057 4
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0882-2025·2025-06-11

    Fresh & Ready Foods Roasted Chicken Wheat Sandwich Recall for Listeria

    Fresh & Ready Foods is recalling Roasted Chicken on Wheat Sandwiches (8.5 oz.) because Listeria monocytogenes was detected on food contact surfaces at the manufacturing facility.

    Product
    Fresh & Ready Foods Roasted Chicken on Wheat Sandwich, 8.5oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89292 9
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0909-2025·2025-06-11

    Fresh Take Crave Away Turkey Bacon Club Sandwich Recalled for Listeria

    Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Turkey & Bacon Club Multigrain Sandwiches (6.5oz containers, Best By 05/09/2025–05/19/2025) because Listeria monocytogenes was detected on food contact surfaces in the manufacturing facility.

    Product
    Fresh Take Crave Away Turkey & Bacon Club Multigrain Sandwich; 6.5oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 85889 9
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0908-2025·2025-06-11

    Fresh Take Crave Away Chicken Salad Multigrain Sandwich Recalled for Listeria

    Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Chicken Salad Multigrain Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility.

    Product
    Fresh Take Crave Away Chicken Salad Multigrain Sandwich; 6oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 58558 2
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0868-2025·2025-06-11

    Fresh & Ready Foods Almonds & Chocolate Snack recalled for Listeria

    Fresh & Ready Foods LLC is recalling Almonds & Chocolate Snack 3oz containers due to Listeria monocytogenes detected on food contact surfaces at the manufacturer facility. The product was distributed in the Southwest and to military facilities.

    Product
    Fresh & Ready Foods Almonds & Chocolate Snack, 3oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 90796 8
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0848-2025·2025-06-11

    Fresh & Ready Foods Thai Chicken Ciabatta Sandwich Listeria Recall

    Fresh & Ready Foods LLC is recalling Thai Chicken on Ciabatta Sandwiches due to Listeria Monocytogenes detected on food contact surfaces at the manufacturing facility. The recall affects 139,863 units distributed across the Southwest.

    Product
    Fresh & Ready Foods Thai Chicken on Ciabatta Sandwich, 9 oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 90877 4
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0873-2025·2025-06-11

    Fresh & Ready Foods Beef Cheesesteak Club Sandwich Recall

    Fresh & Ready Foods is recalling Beef Cheesesteak Club Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility. The recall affects 139,863 units distributed to the Southwest and military facilities.

    Product
    Fresh & Ready Foods Beef Cheesesteak Club Sandwich, 7oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 90343 4
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0843-2025·2025-06-11

    Fresh & Ready Foods Artisan Cheese Bistro Box Recall for Listeria

    Fresh & Ready Foods LLC is recalling Artisan Cheese Bistro Boxes (4 oz. plastic containers, UPC 682906899102) due to Listeria monocytogenes detected on food contact surfaces in the manufacturing facility.

    Product
    Fresh & Ready Foods Artisan Cheese Bistro Box, 4 oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89910 2
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0902-2025·2025-06-11

    Fresh Take Crave Away PB&J Sandwiches Recalled for Listeria

    Fresh & Ready Foods LLC is recalling Fresh Take Crave Away PB&J on Country White sandwiches because Listeria Monocytogenes was detected on food contact surfaces in the manufacturing facility.

    Product
    Fresh Take Crave Away PB&J on Country White; 6oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 61116 8
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0910-2025·2025-06-11

    Fresh Take Tuna Mac Pasta Recalled for Listeria Contamination Risk

    Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Mike's Tuna Mac Pasta (9.5oz containers, Best By dates 05/09/2025–05/19/2025) because Listeria monocytogenes was detected on food contact surfaces at the manufacturer's facility.

    Product
    Fresh Take Crave Away Mike's Tuna Mac Pasta; 9.5oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 58560 5
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0456-2025·2025-06-11

    Fluoxetine Tablets 20 mg Recalled for N-Nitroso Impurity

    Torrent Pharma Inc. is recalling Fluoxetine Tablets, USP, 20 mg in a 28-count carton due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1893-2025·2025-06-11

    Signature Laparoscopic Dolphin Nose Grasper Instrument Insulation Defect

    Silex Medical is recalling 2 units of a Signature Laparoscopic Instruments Dolphin Nose Grasper with Rotating Shaft due to incomplete insulation on the shaft, leaving an exposed area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5860020.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1897-2025·2025-06-11

    Signature Laparoscopic Bullet Tip Grasper Instrument Insulation Defect Recall

    Silex Medical is recalling 6 units of the Signature Laparoscopic Bullet Tip Grasper with Rotating Shaft due to incomplete insulation on the shaft near the rotator wheel, which could expose users to electrical hazards.

    Product
    Signature Laparoscopic Instruments, Bullet Tip Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863030.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1906-2025·2025-06-11

    Dexcom G7 iOS App version 2.7.0 stops updating glucose readings

    Dexcom G7 iOS App version 2.7.0 can enter a state where glucose readings freeze and alerts do not trigger, risking missed detection of dangerously high or low blood sugar. Other connected devices like Apple Watch and insulin pumps continue to receive glucose data directly from the transmitter.

    Product
    Dexcom G7 iOS Application, Ref: SW12300 used in conjunction with the Dexcom G7 Continuous Glucose Monitoring (CGM) system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1899-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Instrument Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.

    Product
    Signature Laparoscopic Instruments, Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5864000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1887-2025·2025-06-11

    Palindrome Precision SI Chronic Hemodialysis Catheter Sterile Barrier Recall

    Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.

    Product
    Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V387000·2025-06-11

    Rivian R1S and R1T front turn signals may fail to illuminate

    Rivian is recalling certain 2025 R1S and R1T vehicles because one or both front turn signals may fail to illuminate and flash, failing FMVSS 108. 27,882 units affected.

    Product
    RIVIAN — RIVIAN R1S, R1T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1886-2025·2025-06-11

    Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.

    Product
    Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1894-2025·2025-06-11

    Signature Laparoscopic Allis Clamp Grasper with Rotating Shaft Recalled

    Silex Medical is recalling the Signature Laparoscopic Instruments Allis Clamp Grasper due to incomplete insulation on the shaft, leaving an exposed area that could pose an electrical hazard during surgical procedures.

    Product
    Signature Laparoscopic Instruments, Allis Clamp Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862030.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2025·2025-06-11

    MAHURKAR Chronic Hemodialysis Catheter recalled for sterile barrier defect

    Mozarc Medical is recalling MAHURKAR Chronic Hemodialysis Catheter Sport Pack units due to a potential breach in sterile barrier packaging that could compromise the product's sterility.

    Product
    MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1903-2025·2025-06-11

    Luminex VERIGENE Gram Negative Blood Culture Test Recalled

    Luminex is recalling VERIGENE Gram Negative Blood Culture test cartridges due to a consumable issue that may produce incorrect results on a small portion of one lot.

    Product
    VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System; invitro diagnostic test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1900-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, 20mm Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5881033.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1911-2025·2025-06-11

    Olympus EVIS EXERA III Duodenovideoscope TJF-Q190V Contamination Risk

    Olympus is recalling the EVIS EXERA III Duodenovideoscope Model TJF-Q190V due to post-market data showing higher microbial contamination when manual cleaning is delayed beyond one hour after patient use.

    Product
    Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1885-2025·2025-06-11

    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical US LLC is recalling Palindrome Precision Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. Affected units were distributed worldwide including the US, Canada, and Mexico.

    Product
    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1910-2025·2025-06-11

    ChannelCheck Convenience Pack Pre-filled Water Syringes Recalled

    Healthmark Industries is recalling ChannelCheck Convenience Pack Pre-filled Water Syringes (Models UCC-222CP and UCC-222-ESP) because contamination was found in duodenoscope samples linked to the syringes, which were improperly used outside their intended purpose.

    Product
    ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample)
    Category
    Medical Device
    Distribution
    Distributed nationwide