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.

25901–25925 of 50450

  • HighFDA (Devices)·Z-1425-2019·2019-05-29

    Zimmer GmbH Recalls 26mm Orthopedic Drill Due to Material Concerns

    Zimmer GmbH is recalling specific orthopedic drills because they may have been manufactured from a different material than specified.

    Product
    Drill, 26mm stop, 1.4x81mm, AO, Item Number 502015146
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1393-2019·2019-05-29

    Boston Scientific Recalls Auriga XL 4007 Laser Systems Due to Power Degradation

    Boston Scientific is recalling three Auriga XL 4007 laser systems because a mechanical cooling issue may cause faster-than-normal power degradation and low power errors.

    Product
    AURIGA XL 4007 GENERAL - DEMO SYSTEM UPN: M0068FS4007GD0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber optic delivery system is intended to be used in surgical procedures such as open, laparoscopic and endoscopic, to…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1457-2019·2019-05-29

    Zimmer CBS 4.5 Countersink Recalled for Potential Material Deviation

    Zimmer GmbH is recalling CBS 4.5 countersinks because they may have been manufactured from a different material than specified.

    Product
    CBS 4.5 countersink, cannulated, 18mm stop, round-shaft, Item Number 503004351
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1423-2019·2019-05-29

    Zimmer GmbH Recalls 2.5x135mm AO Drills Due to Material Concerns

    Zimmer GmbH is recalling 2.5x135mm AO Drills because they may be made from a different material than specified. The products were distributed to 41 US states.

    Product
    Drill, 2.5x135mm, AO, Item Number 502015142
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1413-2019·2019-05-29

    Zimmer GmbH Recalls Drill System Due to Potential Material Deviation

    Zimmer GmbH is recalling Drill Sys 2.7 units because they may have been manufactured from a material different from specifications.

    Product
    Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-1391-2019·2019-05-29

    Trader Joe's Vegetable Melange Recalled for Undeclared Milk Allergen

    Ardo N.V. is recalling Trader Joe's Vegetable Melange in Seasoned Butter Sauce because the label lists butter but fails to declare milk.

    Product
    Trader Joe s Vegetable Melange In Seasoned Butter Sauce Packed in 16 ounce plastic packages retail packaging Bar code: 0033 7038
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1427-2019·2019-05-29

    Zimmer GmbH Recalls 2.7mm Orthopedic Drills Due to Material Concerns

    Zimmer GmbH is recalling specific 2.7mm orthopedic drills because an investigation found they may be made from a different material than specified.

    Product
    Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1420-2019·2019-05-29

    Zimmer GmbH Recalls 19mm Orthopedic Drills Due to Material Concerns

    Zimmer GmbH is recalling specific 19mm orthopedic drills because they may be made from the wrong material. The devices were distributed to 38 US states.

    Product
    Drill, 19mm stop, 1.9x87mm, AO, Item Number 502015131
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1459-2019·2019-05-29

    Zimmer GmbH Recalls CBS 4.0 Countersink Due to Material Concerns

    Zimmer GmbH is recalling CBS 4.0 countersinks because they may have been manufactured from a different material than specified.

    Product
    CBS 4.0 countersink, cannulated, 30mm stop, AO, Item Number 503004353
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1473-2019·2019-05-29

    Zimmer GmbH Recalls 2.7mm AO Drills Due to Material Concerns

    Zimmer GmbH is recalling 2.7x125mm AO drills because they may be made from the wrong material. The devices were distributed to 40 US states.

    Product
    Drill, 2.7x125mm, AO , Item Number ST502015217
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-1393-2019·2019-05-29

    Haikui Abalone in Brown Sauce Recalled for Undeclared Oyster Sauce

    Haiku(Us) Mr Ocean Seafood Corp. is recalling Haikui Abalone in Brown Sauce due to undeclared oyster sauce, a potential allergen.

    Product
    Haikui Abalone in Brown Sauce 3 oz pouch bag,UPC Code: 719926149198
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1424-2019·2019-05-29

    Zimmer GmbH Recalls Stryker 26mm Drill Due to Material Concerns

    Zimmer GmbH is recalling Stryker 26mm drills because they may be made from the wrong material. The products were distributed to 39 US states.

    Product
    Drill, 26mm stop, 1.4x94mm, stryker, Item Number 502015145
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Food)·F-1392-2019·2019-05-29

    Trader Joe's Fire Roasted Vegetables Recalled for Undeclared Milk Allergen

    Ardo N.V. is recalling Trader Joe's Fire Roasted Vegetables with Balsamic Butter Sauce because the label lists butter but fails to declare milk.

    Product
    Trader Joe s Fire Roasted Vegetables With Balsamic Butter Sauce Packed in 16 ounce plastic packages retail packaging Bar code: 0077 5175
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1439-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Material Specification Concerns

    Zimmer GmbH is recalling specific cannulated drills because an investigation found they may have been manufactured from a different material than defined in specifications.

    Product
    Drill, cannulated, 2.5x95mm, AO, Item Number 502015621
    Category
    Medical Device
    Distribution
    42 states
  • HighNHTSA·19V399000·2019-05-29

    HINO 268 and 338 Vehicles Recalled for Backup Camera Display Defect

    ITI is recalling 2018-2019 HINO 268 and 338 vehicles because backup camera displays may revert to factory settings, causing reversed images and increasing crash risk.

    Product
    HINO — HINO 268, 338
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1368-2019·2019-05-29

    Roche Cobas infinity Software Recall for Missing Quality Control Alarms

    Roche Diagnostics is recalling 15 units of Cobas infinity software versions 2.0 through 2.5 because quality control alarms may fail to display after a bottle change.

    Product
    Cobas¿ infinity central lab IT solution Material Number: 07154003001 Calculator/Data Processing Module, For Clinical Use
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-1453-2019·2019-05-29

    Zimmer GmbH Recalls CBS 7.5 Tap Due to Material Concerns

    Zimmer GmbH is recalling CBS 7.5 taps because they may be made from the wrong material. The products were distributed to 41 US states.

    Product
    CBS 7.5 tap, cannulated, AO, Item Number 503002041
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-1476-2019·2019-05-29

    Zimmer GmbH Recalls Cannulated Drills Due to Potential Material Deviation

    Zimmer GmbH is recalling specific cannulated drills because they may have been manufactured from a different material than specified. The products were distributed to 41 US states.

    Product
    Drill, cannulated, 2x95mm, round shaft, Item Number ST502015619
    Category
    Medical Device
    Distribution
    42 states
  • HighNHTSA·19V398000·2019-05-29

    LGE Coachworks Recalls 2018-2019 Ford and Freightliner Vans for Camera Defect

    LGE Coachworks is recalling 2018-2019 Ford and Freightliner vans because back-up camera displays may revert to factory settings, reversing the image and increasing crash risk.

    Product
    FORD — FORD, FREIGHTLINER F-550, BUSINESS CLASS M2, F-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V400000·2019-05-29

    PL Custom Recalls 2017-2019 Ambulances Due to Reversed Backup Camera Image

    PL Custom is recalling 2017-2019 Type I and III ambulances because backup camera monitors may revert to factory settings, reversing the image and increasing crash risk.

    Product
    PL CUSTOM — PL CUSTOM TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide