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.

29976–30000 of 50499

  • HighFDA (Devices)·Z-0467-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail 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 130 DEG 11MM X 360MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0693-2018·2018-02-07

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

    Hom'ade Foods is recalling Mary B's Thins biscuits because they may be contaminated with Listeria monocytogenes. Consumers should check their packages for specific dates and codes.

    Product
    Mary B's Thins , 22 Biscuits, NET WT. 28.3 oz (1LB 12.3 OZ) 810g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0430-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect

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

    Product
    Affixus Hip Fracture Nail, LH 125 DEG 9MM X 440MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0439-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect

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

    Product
    Affixus Hip Fracture Nail, LH 130 DEG 11MM X 460MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0480-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect

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

    Product
    Affixus Hip Fracture Nail, RH 130 DEG 9MM X 360MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0379-2018·2018-02-07

    Carl Zeiss Metrotom 800 CT Scanner Recalled for Software Error

    Carl Zeiss Metrology Inc. is recalling 13 Metrotom 800 industrial CT scanners in the US and Canada due to a software error that causes the system to resume scanning automatically when the access door is closed.

    Product
    Metrotom 800 (130kV CT scanner) Industrial CT scanner for measuring and inspecting complete components made of plastic or light metal.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0754-2018·2018-02-07

    Wegmans Lobster and Shrimp Steam Pot Recalled for Undeclared Soy

    Wegmans is recalling Ready To Cook Lobster & Shrimp Steam Pot because it may contain undeclared soy lecithin.

    Product
    Wegmans Ready To Cook Lobster & Shrimp Steam Pot, Sold by the lb. UPC: 2-16326-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0427-2018·2018-02-07

    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 caused set screws and sleeves to shift, potentially preventing proper assembly.

    Product
    Affixus Hip Fracture Nail, LH 125 DEG 9MM X 260MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0428-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because set screws and sleeves were found out of place during rework, potentially preventing proper assembly.

    Product
    Affixus Hip Fracture Nail, LH 125 DEG 9MM X 340MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0452-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect

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

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 13MM X 260MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0692-2018·2018-02-07

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

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

    Product
    Mary B's Butter Taste, 20 Biscuits, Value Pack, NET WT. 44 oz (2LB 12 OZ)1247g; and Mary B's Butter Taste, 30 Biscuits, Family Pack, NET WT. 60 oz (3LB 12 OZ) 1701g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0448-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect

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

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 11MM X 300MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0455-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

    Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework error may have displaced set screws and sleeves, potentially preventing proper assembly.

    Product
    Affixus Hip Fracture Nail, RH 125 DEG 9MM X 320MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0440-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail 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, LH 130 DEG 13MM X 460MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0466-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail 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 130 DEG 11MM X 340MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0690-2018·2018-02-07

    Mary B's Southern Made Biscuits Recalled for Listeria Risk

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

    Product
    Mary B's Southern Made, 12 Biscuits, NET WT. 26.4 oz (1LB 10.4OZ) 748g; Mary B's Southern Made, 20 Biscuits, Value Pack, NET WT. 44 oz (2LB 12 OZ) 1247g; and Mary B's Southern Made, 30 Biscuits, Family Pack, NET WT. 60 oz (3LB 12 OZ) 1701g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0468-2018·2018-02-07

    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 130 DEG 11MM X 380MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0445-2018·2018-02-07

    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 caused set screws and sleeves to shift, potentially preventing proper assembly.

    Product
    Affixus Hip Fracture Nail, LH 130 DEG 9MM X 400MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0432-2018·2018-02-07

    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 11MM X 280MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0483-2018·2018-02-07

    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 during rework, potentially preventing proper assembly.

    Product
    Affixus Hip Fracture Nail, RH 130 DEG 9MM X 420MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0446-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail 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, LH 130 DEG 9MM X 420MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0420-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Assembly Defect

    Zimmer Biomet is recalling 638 units of the Affixus Hip Fracture Nail because a set screw and sleeve assembly may have shifted during rework, potentially preventing proper installation.

    Product
    Affixus Hip Fracture Nail, 125 DEG 11MM X 180MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0482-2018·2018-02-07

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Assembly Defect

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

    Product
    Affixus Hip Fracture Nail, RH 130 DEG 9MM X 400MM
    Category
    Medical Device
    Distribution
    Distributed nationwide