The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

29926–29950 of 50499

  • HighFDA (Devices)·Z-0514-2018·2018-02-14

    Philips Precedence 16 Imaging System Recalled for Collimator Drop Risk

    Philips is recalling 1,387 Precedence 16 imaging systems because collimators may drop to the floor during exchange, posing a physical hazard.

    Product
    Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Griffin) is an imaging system combining the acquisition of single photon nuclear medicine images and images from an x-ray computed tomography system. Precedence may produce non-attenuation corrected and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0715-2018·2018-02-14

    Wienke's Market Whole Cherry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Whole Cherry Jam because it contains butter that is not listed on the label.

    Product
    Wienke's Market Whole Cherry Jam, Net Wt. 8 oz (226g), UPC 14106-00212. Refrigerate after opening. Ingredients: cherries, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-0787-2018·2018-02-14

    Stevens Bakery Recalls Toll House Pies for Undeclared Milk

    Stevens Family Bakery & Orchard LLC is recalling Toll House Pies because the label failed to declare milk ingredients found in butter.

    Product
    Toll House Pie Baked whole/half pies & frozen pies, Stevens Bakery & Orchard ,7344 Thackery Road, Springfield, Ohio 45502, (937) 788-2873
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0782-2018·2018-02-14

    Stevens Bakery Peach Pies Recalled for Undeclared Milk Allergen

    Stevens Family Bakery & Orchard LLC is recalling 15 baked peach pies sold in Ohio because the label failed to list butter, an undeclared milk allergen.

    Product
    Peach Pie Baked whole pies & Baked 1/2 pies, Stevens Bakery & Orchard, 7344 Thackery Road, Springfield, Ohio 45502, (937) 788-2873
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0722-2018·2018-02-14

    Wienke's Market Cranberry Cherry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Cranberry Cherry Jam because it contains butter, an ingredient not declared on the label.

    Product
    Wienke's Market Cranberry Cherry Jam, Net Wt. 8 oz (226g), UPC 14106-00218. Refrigerate after opening. Ingredients: cranberries, cherries, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • HighCPSC·18097·2018-02-13

    Tea Collection Recalls Children's Rompers Due to Choking Hazard

    Tea Collection is recalling about 3,800 children's rompers because snaps near the collar can detach, posing a choking hazard to young children.

    Product
    Children's rompers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V103000·2018-02-09

    Mitsubishi Recalls Outlander Sport for Wiper Link Corrosion Risk

    Mitsubishi is recalling 2011-2016 Outlander Sport vehicles because water intrusion may corrode the wiper link, causing wipers to stop working and reducing visibility.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V102000·2018-02-09

    Volkswagen Recalls 2017-2018 Tiguan Limited for Incorrect Front Driver Air Bag

    Volkswagen is recalling 2017-2018 Tiguan Limited vehicles because the front driver air bag may not be intended for US use, failing federal safety standards and increasing injury risk in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18723·2018-02-08

    Poppin Recalls Pitch Rolling Chairs Due to Fall Hazard

    Poppin is recalling about 2,800 Pitch rolling chairs because the seat plate can break and detach, posing a fall hazard. No injuries have been reported.

    Product
    Pitch rolling chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V098000·2018-02-08

    Chrysler Recalls 2017 Jeep Wrangler and Dodge Caravan for Brake Switch Defect

    Chrysler is recalling 2017 Jeep Wrangler and Dodge Caravan vehicles because brake switches may malfunction, allowing the vehicle to shift out of Park without the brake pedal being pressed.

    Product
    JEEP — JEEP, DODGE WRANGLER, CARAVAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18095·2018-02-08

    Husqvarna Recalls Zero Turn Riding Mowers Due to Fire Hazard

    Husqvarna is recalling about 7,100 residential zero turn riding mowers because a fuel line defect can cause leaks and fire. No injuries have been reported.

    Product
    Residential zero turn riding mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V100000·2018-02-08

    RAM Trucks Recalled for Transmission Shift Interlock Defect

    Chrysler is recalling 2017-2018 RAM trucks because the brake pedal interlock may fail, allowing the vehicle to shift out of Park without the brake pedal being pressed.

    Product
    RAM — RAM 2500, 5500, 1500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2018·2018-02-07

    Beaver Safety Sideport Knife Recalled Due to Retracted Protective Shield

    Beaver-Visitec International Inc. is recalling specific batches of Beaver Safety Sideport Knives because the protective shield retracted, exposing the blade.

    Product
    bvi Beaver Safety Sideport Knife: (a) 1.0mm, 45o, REF 378210 (b) 1.2mm, 45o, REF 378212 (c) 115mm, 45o, REF 378231 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0691-2018·2018-02-07

    Mary B's Tea Biscuits Recalled for Potential Listeria Contamination

    Hom'ade Foods is recalling Mary B's Tea Biscuits due to potential Listeria monocytogenes contamination. Consumers should check their packages for specific dates and codes.

    Product
    Mary B's Tea Biscuits, 24 Biscuits, Bite-Sized, NET WT. 24 oz (1LB 8 OZ) 680g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0447-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process may have displaced internal components, potentially preventing proper assembly.

    Product
    Affixus Hip Fracture Nail, LH 130 DEG 9MM X 440MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0460-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent the set screw and sleeve assembly from staying in place.

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 9MM X 440MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0752-2018·2018-02-07

    Wegmans Garlic Parmesan Tilapia Recalled for Undeclared Soy Lecithin

    Wegmans is recalling specific packages of Ready To Cook Garlic Parmesan Tilapia because they may contain undeclared soy lecithin, a common allergen.

    Product
    Wegmans Ready To Cook Garlic Parmesan Tilapia, Single, 5 oz UPC: 2-16150-00000 and Wegmans Ready To Cook Garlic Parmesan Tilapia, Twin Pack, 15 oz UPC: 2-16154-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0451-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing defect may prevent proper assembly of the device.

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 11MM X 460MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0502-2018·2018-02-07

    Beaver Xstar Safety Slit Knives Recalled Due to Retracted Protective Shield

    Beaver-Visitec International Inc. is recalling 659,370 units of bvi Beaver Xstar Safety Slit Knives because the protective shield was retracted, exposing the blade.

    Product
    bvi Beaver Xstar Safety Slit Knife: (a) REF 378214, 1.4mm, 45o Bevel Up (b) REF 378215, 1.50mm, 45o Bevel Up (c) REF 378217, 1.7mm, 45o Bevel Up (d) REF 378218, 1.8mm, 45o Bevel Up (e) REF 378220, 2.0mm, 45o Bevel Up (f) REF 378222, 2.2mm, 45o Bevel Up (g) REF 378223…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0459-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may not be in the correct location, potentially preventing proper product assembly.

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 9MM X 420MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0688-2018·2018-02-07

    Hom'ade Foods Recalls Mary B's Jumbo Biscuits for Listeria Risk

    Hom'ade Foods is recalling Mary B's Jumbo Biscuits because they may be contaminated with Listeria monocytogenes. Consumers should check their pantries for affected products.

    Product
    Mary B's Jumbo, 10 Biscuits, Extra Large, NET WT. 35 oz (2LB 3OZ) 992g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0453-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may have shifted, preventing proper product assembly.

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 13MM X 320MM
    Category
    Medical Device
    Distribution
    Distributed nationwide