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.

27126–27150 of 50462

  • HighFDA (Food)·F-0246-2019·2018-10-31

    McCain Foods Recalls Caramelized Mushroom Slices Due to Listeria and Salmonella

    McCain Foods USA is recalling 244 cases of Jon-Lin Caramelized Mushroom Slices because the product was released after presumptive positive tests for Listeria monocytogenes and Salmonella.

    Product
    Caramelized Mushroom Slices; Sold in 25 lb. containers. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0231-2019·2018-10-31

    McCain Foods Recalls Pepper Strips Due to Listeria and Salmonella Testing Issues

    McCain Foods USA is recalling Fire-Roasted Homestyle Julienne Tri-Colored Pepper Strips because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire-Roasted Homestyle Julienne Tri-Colored Pepper Strips; Sold in 20 lb. containers. Brand Name:Jon-Lin¿ NatureSmart¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0229-2019·2018-10-31

    McCain Foods Recalls Diced Sweet Onions Due to Listeria and Salmonella Testing

    McCain Foods USA is recalling 23,203 cases of Dark Caramelized Diced Sweet Onions because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Dark Caramelized 3/8" Diced Sweet Onions; Sold in 20 lb. containers. Brand Name:Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0208-2019·2018-10-31

    DePuy Mitek Screw and Washer Depth Gauge Recalled for Design Offset

    DePuy Mitek is recalling 401 Mitek Screw and Washer Depth Gauges because a design offset causes readings to be approximately 3.2mm shorter than the actual bone hole length.

    Product
    Mitek Screw and Washer Depth Gauge, Product Code 219024
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0324-2019·2018-10-31

    McCain Foods Recalls Fire-Roasted Diced Jalapenos Due to Listeria and Salmonella Risks

    McCain Foods USA is recalling Fire-Roasted 1/4" Diced Jalapenos because products were released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire-Roasted 1/4" Diced Jalapenos;: Sold in 25 lb. containers. Brand Name: Jon-Lin¿ NatureSmart"
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0102-2019·2018-10-31

    Teva Recalls Pioglitazone and Metformin Tablets Due to Defective Delivery System

    Teva Pharmaceuticals USA is recalling specific lots of Pioglitazone and Metformin tablets because some may lack laser drilling, potentially affecting drug release.

    Product
    PIO&METFORMIN 15/1000 mg Tab 1 (Pioglitazone and Metformin XT) tablets, Takeda Brand Name: Actoplus Met XR (Pioglitazone and metformin HCl extended -release) tablets, 15 mg/1000 mg, packaged in a fiber drum, Application Holder Takeda Pharmaceuticals, U.S.A. Inc. One Takeda…
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0241-2019·2018-10-31

    Custom Healthcare Systems Recalls Injection Trays Due to Sterility Compromise

    Custom Healthcare Systems is recalling 40 units of CHS Custom Convenience Kit-INJECTION TRAY because incorrect sealing specifications compromised product sterility.

    Product
    CHS Custom Convenience Kit-INJECTION TRAY Product Number: B9-17201
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0236-2019·2018-10-31

    McCain Recalls Fire-Roasted Cauliflower Due to Listeria and Salmonella Testing Issues

    McCain Foods USA is recalling Fire-Roasted Cauliflower Florets because products were released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire-Roasted Cauliflower Florets ; Sold in 25 lb. containers. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0207-2019·2018-10-31

    Howmedica Recalls Tritanium TL Steerable Inserter Due to Locking Mechanism Failure

    Howmedica Osteonics Corp. is recalling 58 units of the Tritanium TL Steerable Inserter because the locking mechanism may fail to function as intended due to lack of lubrication.

    Product
    Tritanium TL Steerable Inserter, Cat. No. 48930000, UDI 07613327381900 Product Usage: The TL Steerable Inserter is a Class 1 instrument which is provided in a non-sterile condition. The inserter is designed to enter the disc space, with a fixed engagement between the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0260-2019·2018-10-31

    Custom Healthcare Systems Recalls Penrose Drain Kits Due to Sterility Compromise

    Custom Healthcare Systems is recalling 24 units of Penrose Drain Convenience Kits because incorrect sealing specifications compromised product sterility.

    Product
    CHS Custom Convenience Kit- PENROSE DRAIN (.75" X 18") Product Number:D8-9425B
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0216-2019·2018-10-31

    Siemens StreamLab Refrigerated Storage Module Recall for Missing Warning Label

    Siemens Healthcare Diagnostics is recalling StreamLab Refrigerated Storage Module 9000 units because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.

    Product
    STREAMLAB - REFRIGERATED STORAGE MODULE 9000
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-0210-2019·2018-10-31

    McCain Recalls Fire-Roasted Portobello Mushrooms Due to Listeria and Salmonella Testing Issues

    McCain Foods USA is recalling Fire-Roasted Thin Sliced Portobello Mushrooms because products were released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    FIRE-ROASTED THIN SLICED PORTOBELLO MUSHROOMS: Sold in 2 lb. . packages. Brand Name: Jon-Lin¿ NatureSmart¿;
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0241-2019·2018-10-31

    McCain Recalls Fire-Roasted Pepper and Onion Blend Due to Listeria and Salmonella

    McCain Foods USA is recalling Fire-Roasted Pepper and Onion Blend because products were released after presumptive positive tests for Listeria monocytogenes and Salmonella without confirmation.

    Product
    Fire-Roasted Pepper and Onion Blend; Sold in 300 lb. containers. Brand Name: Jon-Lin¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0250-2019·2018-10-31

    CHS Custom Convenience Kits Recalled for Sterility Compromise

    Custom Healthcare Systems is recalling 630 CHS Custom Convenience Kits because incorrect sealing specifications compromised product sterility.

    Product
    CHS Custom Convenience Kit-GENERAL UTILITY TRAY Product Number:S1528-02
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0212-2019·2018-10-31

    Siemens APTIO 15000 Refrigerated Storage Module Recall for Missing Warning Label

    Siemens Healthcare Diagnostics is recalling 441 APTIO 15000 Refrigerated Storage Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.

    Product
    APTIO 15000 REFRIGERATED STORAGE MODULE
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0249-2019·2018-10-31

    Custom Healthcare Systems Recalls Vaginal Speculums Due to Sterility Compromise

    Custom Healthcare Systems is recalling vaginal speculums because incorrect sealing specifications compromised product sterility.

    Product
    (1)CHS Custom Convenience Kit-VAGINAL SPECULUM (SMALL) Product Number:D36-16267 (2) CHS Custom Convenience KitVAGINAL SPECULUM (LARGE) Product Code: D36-16269
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0240-2019·2018-10-31

    McCain Pizza Kitchen Cut Medley Recalled for Listeria and Salmonella Risk

    McCain Foods USA is recalling 4,620 cases of Jon-Lin NatureSmart Pizza Kitchen Cut Medley because products were released after presumptive positive tests for Listeria monocytogenes and Salmonella.

    Product
    Pizza Kitchen Cut Medley; Sold in 25 lb. containers. Brand Name: Jon-Lin¿ NatureSmart"
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0215-2019·2018-10-31

    Siemens StreamLab Automation Modules Recalled for Missing Pacemaker Warning Label

    Siemens Healthcare Diagnostics is recalling 186 StreamLab Automation Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.

    Product
    STREAMLAB CORE UNIT / LYNX WITH IOM
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0197-2019·2018-10-31

    Shimadzu TRINIAS Digital Angiographic System Recalled for C-Arm Movement Issue

    Shimadzu is recalling one TRINIAS Digital Angiographic System in Louisiana due to a software issue that may cause the C-arm to move unexpectedly, posing a risk of contact with patients or staff.

    Product
    TRINIAS Digital Angiographic System intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and whole body radiographic/fluoroscopic procedures.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0247-2019·2018-10-31

    McCain Recalls Fire-Roasted Elote Corn Blend Due to Listeria and Salmonella

    McCain Foods USA is recalling Fire-Roasted Rubio's Elote Corn Blend because finished product was released after presumptive positive tests for Listeria monocytogenes and Salmonella.

    Product
    Fire-Roasted Rubio's Elote Corn Blend; Sold in 2 lb. containers. Brand Name: Chef Sensations¿
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0212-2019·2018-10-31

    McCain GFGB Roasted Vegetable Blend Recalled for Listeria and Salmonella

    McCain Foods USA is recalling GFGB Roasted Vegetable Blend after internal audits revealed products were released with presumptive positive tests for Listeria and Salmonella.

    Product
    Roasted Vegetable Blend: Sold in 2 lb. . packages. Brand Name: GFGB
    Category
    Food
    Distribution
    0 states