The Recall Desk

Hazard

Class I recalls

702 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all class i recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

626–650 of 702

  • SevereFDA (Food)·H-0265-2025·2025-07-23

    Chopped red bell peppers recalled over potential Listeria monocytogenes contamination

    Chopped red bell peppers packed in polybags and cardboard cases are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 31 cases are affected.

    Product
    FG20007 Pepper, Red Bell Chop packaged in poly bag, and cardboard case. 17.5 lbs per case
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0306-2025·2025-07-23

    Danshi shredded tofu recalled because sesame is not declared on label

    Danshi branded Shredded Tofu 200g is being recalled because the product does not declare the allergen ingredient sesame. 50 cases are affected.

    Product
    Front Panel: Danshi branded Shredded Tofu, 200g Rear Panel: Best before: 05/24/2025, Imported by: Shang Hao Jia, Inc. Address: South El Monte, CA 91733. Product of China. Manufacturer: Sichuan Shifang Danshi Food Co., Ltd. UPC: 6 942849 709499
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0317-2025·2025-07-23

    Peeters Mushroom Farm thick sliced mushrooms recalled over potential Listeria contamination

    Peeters Mushroom Farm Thick Slice Mushrooms in 10 lb containers are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 10 cases are affected.

    Product
    Peeters Mushroom Farm Thick Slice Mushroom 10lb cardboard container labeled with Peeters Mushroom Farm
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0214-2025·2025-07-16

    Garlic cheddar cheese curds recalled over potential Listeria monocytogenes contamination

    Vampire Slayer Garlic Cheddar Cheese Curds are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 260 cases are affected.

    Product
    VAMPIRE SLAYER Garlic Cheddar Cheese Curds, net wt. 6 oz. Product is package in a sealed plastic cup with lid. UPC on 6oz. retail cup: 8 51222 00528 7. FaceRockCreamery.com MASTER CASE's label is read in parts: Item No. 240062 Vampire Slayer Curds 12/6oz., net wt. 4.5 lbs. Face
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0213-2025·2025-07-16

    JLM dark chocolate nonpareils recalled over undeclared milk allergen

    JLM Manufacturing Dark Chocolate Nonpareils in 14 oz tubs are being recalled because of undeclared milk. 971 cases are affected, distributed nationwide.

    Product
    JLM Manufacturing Dark Chocolate Nonpareils, 14oz clear plastic tub, UPC 7 60208 12450 1, item # 392303, 12 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2032-2025·2025-07-16

    Hillrom LikoScale patient lift components may falsely latch and detach

    Hillrom LikoScale components used with patient lift adapter kits are being recalled because the Q-link 13 may allow false latching of the quick-release hook. 9,839 units are affected.

    Product
    Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code 3156225; 2) LikoScale 350 Accessory - Product Code 3156228; 3) LikoScale 400 Accessory - Product Code 3156226.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2047-2025·2025-07-16

    Bravo CF capsule delivery devices may have misapplied adhesive causing malfunction

    The Bravo CF capsule delivery device is being recalled because misapplied adhesive may prevent the pH capsule attaching to the oesophagus or detaching from the delivery device. 128,202 units affected.

    Product
    Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2084-2025·2025-07-16

    FEM-FLEX II FEMII018A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 13,240 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2080-2025·2025-07-16

    Optisite OPTI16 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI16 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 27,022 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0216-2025·2025-07-16

    Weaver white seed nonpareil chocolate recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate (White Seeds) in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 1,760 cases are affected.

    Product
    Weaver Chocolates, D2645 - Nonpareil, Semi-Sweet Chocolate (White Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2081-2025·2025-07-16

    Optisite OPTI18 arterial cannulas may have wire protruding from the body

    Edwards Optisite OPTI18 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 13,240 units affected.

    Product
    Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI18 Software Version: N/A Product Description: Cardiac cannula. The Edwards OptiSite Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorpo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0221-2025·2025-07-16

    Whole organic celery seed recalled over potential Salmonella contamination

    Whole Organic Celery Seed is being recalled because of potential contamination with Salmonella. 439 bags totalling 24,694 lbs are affected.

    Product
    Celery Seed Whole Organic, labeled, "CELERY SEED WHL OG; Net Wt: 56.25 Lbs"
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2031-2025·2025-07-16

    Hillrom Q-Link 13 patient lift components may falsely latch and detach

    The Hillrom Q-Link 13 component used with mobile patient lifts is being recalled because it may allow false latching of the quick-release hook. 9,899 units are affected.

    Product
    Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts: 1) Uno 102 EE Mobile lift - Product Code 2010004; 2) Viking L Mobile lift - Product Code 2040044; 3) Viking XL Mobile lift - Product Code 2040043; 4) Viking M Mobile lift -
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·H-0215-2025·2025-07-16

    Weaver bulk semi-sweet chocolate nonpareils recalled over undeclared milk allergen

    Weaver Chocolates Nonpareil Semi-Sweet Chocolate in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 849 cases are affected.

    Product
    Weaver Chocolates, 47518 - Nonpareil, Semi-Sweet Chocolate (Christmas Seeds) - 25 lbs. Bulk Cases
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2085-2025·2025-07-16

    FEM-FLEX II FEMII018AS cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018AS, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 558 units affected.

    Product
    Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII018AS Software Version: N/A Product Description: The Edwards FEMFLEXII Arterial Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2082-2025·2025-07-16

    FEM-FLEX II FEMII016A cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII016A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 6,801 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2083-2025·2025-07-16

    FEM-FLEX II femoral arterial cannulas may have wire protruding from body

    Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.

    Product
    Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016AS Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae provides or establishes arterial perfusion in the extracorporeal circuit for d 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0122-2025·2025-07-09

    Zenshi California roll trays made with recalled cucumbers

    Zenshi Handcrafted Sushi California Roll is being recalled because it was made with cucumbers recalled over possible Salmonella. 39,743 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI California Roll 10pc Net Wt. 7.1oz (201g) UPC 0 23012 94264 9, UPC 023012 95138 2 & UPC 0 23012 90618 4
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0177-2025·2025-07-09

    Zenshi mango red rock sushi trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Mango Red Rock is being recalled because it was made with cucumbers recalled over possible Salmonella. 184 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Mango Red Rock 5pc Net Wt. 9.8oz UPC 0 23012 94497 1
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2013-2025·2025-07-09

    Servo-u ventilators may measure patient circuit compliance inaccurately

    The Servo-u Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 874 units are affected.

    Product
    Servo-u Ventilator System. Model Number: 6688600.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0193-2025·2025-07-09

    Zenshi spring sushi wrap trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Spring Sushi Wrap is being recalled because it was made with cucumbers recalled over possible Salmonella. 3,671 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Spring Sushi Wrap 10pc Net Wt. 10.5oz UPC 0 23012 95062 3
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0197-2025·2025-07-09

    Zenshi ultimate chili tuna roll trays made with recalled cucumbers

    Zenshi Handcrafted Sushi Ultimate Chili Roll with tuna is being recalled over cucumbers recalled for possible Salmonella. 1,365 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Ultimate Chili Roll - Tuna 10pc Net Wt. 10.4oz UPC 0 23012 94413 1
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0124-2025·2025-07-09

    Zenshi California salad brown rice rolls made with recalled cucumbers

    Zenshi Handcrafted Sushi California Salad Roll on brown rice is being recalled over cucumbers recalled for possible Salmonella. 240 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI California Salad Roll 10pc (Brown Rice) Net Wt. 7.1oz (201g) UPC 0 23012 94267 & 0 UPC 0 23012 95139 9
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0157-2025·2025-07-09

    Zenshi spicy tuna and crunchy California duo combo used recalled cucumbers

    Zenshi Handcrafted Sushi Duo Combo with Spicy Tuna and Crunchy California Roll is being recalled over cucumbers recalled for possible Salmonella. 902 trays are affected.

    Product
    ZENSHI HANDCRAFTED SUSHI Duo Combo - Spicy Tuna & Crunchy CA Roll 10pc Net Wt 7.6oz UPC 0 23012 94212 0
    Category
    Food
    Distribution
    8 states