The Recall Desk

Severity 5 of 5

Critical recalls

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

What “critical” means here

Severity 5 (Critical) covers recalls where deaths or serious injuries have been reported, or where the agency itself classified the action as the highest severity (FDA Class I, NHTSA 'death/serious injury reported'). These are the recalls you should treat as urgent — stop using the product immediately and follow the agency's guidance. Common Severity-5 categories are pathogen-contaminated ready-to-eat foods (Listeria, E. coli O157, Salmonella), drug products with confirmed adverse-event reports, and vehicle defects with documented fatal crashes.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

276–300 of 7436

  • CriticalFDA (Devices)·Z-0488-2026·2025-11-26

    Jaw joint implants recalled over a discrepancy in screw hole position

    TMJ Solutions is recalling 63 TMJ Bilateral Implants because the patient-fitted temporomandibular joint implant contained a discrepancy in screw hole position. The FDA classified it Class I.

    Product
    TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    15 states
  • CriticalFDA (Food)·H-0197-2026·2025-11-26

    Whatcom Blue cheese recalled over E coli O103 in raw milk

    Peterson Company is recalling 288 pieces of Twin Sisters Creamery Whatcom Blue cheese due to E. coli O103:H2. The FDA has classified the recall as Class I.

    Product
    Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz. There are 16 pieces per case. This cheese is made from raw milk. Ingredients: cultured raw cow's milk, salt, enzymes, penicillium roqueforti. Made by Twin Sisters
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0192-2026·2025-11-26

    Vanilla ice cream recalled over undeclared eggs in four states

    Publix Super Markets is recalling 1,452 units of Publix Rich & Creamy Vanilla Ice Cream over undeclared eggs. The FDA has classified the recall as Class I.

    Product
    Publix Rich & Creamy Vanilla Ice Cream
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0195-2026·2025-11-26

    Peppercorn raw milk cheese recalled over E coli O26 contamination

    Twin Sisters Creamery is recalling 115.46 pounds of raw milk Peppercorn cheese due to E. coli O26:H11. The FDA has classified the recall as Class I.

    Product
    Twin Sisters Creamery Peppercorn cheese, 3lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. Ingredients: cultured raw cow's milk, whole peppercorns, salt, enzymes. Made in Ferndale, WA. www.twinsisterscreamery.com.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-0200-2026·2025-11-19

    Clamshell peach salsa recalled over Listeria risk from supplied peaches

    JFE Franchising is recalling 177 units, 154.88 pounds, of 16 oz peach salsa in clamshells because the peaches supplied by Moonlight Peaches are potentially contaminated with Listeria.

    Product
    Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic clamshells Sell by 11/3/2025 Sell by 11/4/2025
    Category
    Food
    Distribution
    18 states
  • CriticalFDA (Devices)·Z-0431-2026·2025-11-19

    MRI upgrade recalled over ice blockage in helium venting paths

    Siemens Medical Solutions is recalling four MAGNETOM Cima.X Upgrade systems because an ice blockage may form in the magnet's helium venting paths. The FDA has classified it Class I.

    Product
    MAGNETOM Cima.X Upgrade. Model Number: 11689304.
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-0443-2026·2025-11-19

    Breathing kits recalled over cracks in the expandable anesthesia tubing

    Medline is recalling the latex-free Breathing Kit DYNJ10550 after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; BREATHING KIT-LF DYNJ10550
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0179-2026·2025-11-19

    Cashew candy bars recalled over an undeclared peanut allergen

    Zingerman's Coffee Company is recalling 78 units of its 2 oz Ca$hew Cow Candy Bar over undeclared peanut. The FDA has classified the recall as Class I.

    Product
    Zingerman's Ca$hew Cow Candy Bar net wt 2oz UPC 844397000157
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-0178-2026·2025-11-19

    Peanut butter candy bars recalled over an undeclared cashew allergen

    Zingerman's Coffee Company is recalling 156 units of its 2 oz Peanut Butter Crush Candy Bar over undeclared cashew. The FDA has classified the recall as Class I.

    Product
    Zingerman's Peanut Butter Crush Candy Bar net wt 2oz UPC 844397005237
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-0174-2026·2025-11-19

    Italian parsley recalled over potential Salmonella contamination in eight states

    Pacific International Marketing is recalling 308 cases of conventional Italian parsley over potential Salmonella contamination. The FDA has classified the recall as Class I.

    Product
    Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL MARKETING SALINAS, CA 93912 Carton Sticker Label: Conv Italian Parsley 60 Ct Ctn Pacific Product of USA Distributed By: Dynasty Farms Salinas, CA 93905 UPC 40695 80125 Twist Tie (for bunches) Label: FLAT PARSLEY PLU #
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·H-0176-2026·2025-11-19

    Thirty count parsley cases recalled over potential Salmonella contamination

    Pacific International Marketing is recalling 2 cases of 30-count iceless conventional Italian parsley over potential Salmonella. The FDA has classified the recall as Class I.

    Product
    Carton Label: PACIFIC FRESH VEGETABLES PACIFIC INTERNATIONAL MARKETING SALINAS, CA 93912 PRODUCE OF U.S.A. Sticker Label: Conv Italian Parsley 30 Ct Iceless Pacific Product of USA Distributed By: Dynasty Farms Salinas, CA 93905 Twist Tie (for bunches) Label: FLAT PARSLEY PLU #4
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·H-0186-2026·2025-11-19

    Green Maeng Da kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom Green Maeng Da powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom Green Maeng Da powder is packaged in seal mylar pouches: Monarch Premium Kratom Green Maeng Da, 4oz powder (112g), UPC 851006008466 Monarch Premium Kratom Green Maeng Da, 0.5oz powder (14g), UPC 851006008770 Monarch Premium Kratom Green Maeng Da, 2
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0191-2026·2025-11-19

    Strawberry ice cream cones recalled over an undeclared peanut allergen

    Seoul Trading is recalling 78 cases of PIGGY Lotte Crispy Crunch strawberry ice cream cones over undeclared peanut. The FDA has classified the recall as Class I.

    Product
    Item IL1014A, PIGGY Lotte Crispy Crunch Ice Cream Cone, Strawberry flavor, Keep Frozen, (4/5/160ML), UPC 8801118255045. Product of Korea. The label of recalled product declared: Ingredients: Cone snack, Strawberry syrup, Biscuit, Chocolate spray, Topping Chocolate, Ice cream mix
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·H-0177-2026·2025-11-19

    Bagged Italian parsley recalled over potential Salmonella contamination

    Pacific International Marketing is recalling 160 cases of bagged conventional Italian parsley over potential Salmonella. The FDA has classified the recall as Class I.

    Product
    Carton Label: PACIFIC STRAIGHT FROM THE FIELDS FRESH HERBS 4/24 BUNCH ITALIAN PARSLEY BAGS PRODUCE OF U.S.A. PACIFIC INTERNATIONAL MARKETING SALINAS, CA 93912 Carton Sticker Label: Conv Italian Parsley 4/24 CT Display Pacific Product of USA Distributed By: Dynasty Farms Salinas
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Devices)·Z-0445-2026·2025-11-19

    Airway procedure kits recalled over cracks in anesthesia circuit tubing

    Medline is recalling ENT and laryngoscopy-bronchoscopy kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; ENT DYNJ909128I; LARYNGOSCOPY - BRONCHOSCOPY DYNJ909114D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0199-2026·2025-11-19

    Peach salsa recalled over Listeria in peaches from one supplier

    GBC Food Services is recalling 154.88 pounds of 14 oz peach salsa because the peaches supplied by Moonlight Peaches are potentially contaminated with Listeria. The FDA classified it Class I.

    Product
    Peach Salsa; UPC 85006540364 14oz (397g); Use by 10/12/2025 to 10/29/2025
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Devices)·Z-0442-2026·2025-11-19

    Adult anesthesia circuit kits recalled over cracked expandable tubing

    Medline is recalling multiple adult 120-inch expandable anesthesia circuits after complaints of leaks caused by cracks in the tubing. The FDA has classified it Class I.

    Product
    Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers: ADULT 120 EXPANDABLE W/MASK DYNJAA10591; ANES CIRC 120IN EXP-LF DYNJAA6555G; ANES CIRCUIT ADULT 120"-LF DYNJAA10817; ANESTHESIA 120" ADLT-LF DYNJAA10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0447-2026·2025-11-19

    Surgical convenience kits recalled over cracked anesthesia circuit tubing

    Medline is recalling 96,406 breast and hernia convenience kits after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience Kit, BREAST HERNIA DYNJ909125G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0450-2026·2025-11-19

    Robotic surgery kits recalled over cracked anesthesia circuit tubing

    Medline is recalling GYN Robotic and Robotic Prostate convenience kits after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.

    Product
    Convenience kits; DYNJ901046M GYN ROBOTIC DYNJ909120D ROBOTIC PROSTATE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0185-2026·2025-11-19

    Bali Gold kratom powder recalled over potential Salmonella contamination

    Lotus Vaping Technologies is recalling Monarch Premium Kratom Bali Gold powder in 4 oz and 8 oz sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.

    Product
    Monarch Premium Kratom Bali Gold powder is packaged in seal mylar pouches: Monarch Premium Kratom Bali Gold, 4oz powder (112g), UPC 851006008428 Monarch Premium Kratom Bali Gold, 8oz powder (224g), UPC 706970483712
    Category
    Food
    Distribution
    Distributed nationwide