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.

39301–39325 of 50506

  • HighNHTSA·15V180000·2015-03-27

    Blue Bird Recalls 2015-2016 Vision Buses Due to Inverter Fire Risk

    Blue Bird is recalling 2015-2016 Vision non-school transit buses because a voltage inverter failure may produce smoke and increase the risk of a fire.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V182000·2015-03-27

    Western Star Trucks Recall Fire Extinguishers That May Fail to Discharge

    Daimler Trucks North America is recalling 2014-2015 Western Star trucks equipped with certain Kidde fire extinguishers that may not fully discharge.

    Product
    WESTERN STAR — WESTERN STAR 5700, 4900, 6900, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0984-2015·2015-03-25

    Siemens ARTISTE MV System Linear Accelerator Recalled for Software Issue

    Siemens is recalling three ARTISTE MV System linear accelerators due to a software issue that may cause a dark current phenomenon during specific cancer treatments.

    Product
    ARTISTE MV System, Linear Accelerator (LINAC) with SysVC10A software. The intended use of the ARTISTE MV System linear accelerator system is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-1430-2015·2015-03-25

    Rill Foods Recalls Mount Mazama Lentil Chili Due to Peanut Contamination Risk

    Rill Foods is recalling Mount Mazama Lentil Chili because the cumin used may contain peanut protein. Consumers should stop using the product.

    Product
    The product label reads in part "***Mount Mazama Lentil Chili***Rill Foods***NET WT. 15 OZ.***". The product is packaged in a clear flexible laminate bag and the spices in a separate bag within the bag. A card stock topper is attached to the top of the bag after filled. This…
    Category
    Food
    Distribution
    9 states
  • HighCPSC·15103·2015-03-25

    Linon Recalls Foldable Wood Patio Chairs Due to Fall Hazard

    Linon Home Décor is recalling about 3,300 foldable wood patio chairs and bistro sets because they can tip over, causing falls.

    Product
    Outdoor Wood Bistro Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1298-2015·2015-03-25

    CooperSurgical Infant Heel Gel Warmers Recalled for Burn Risk

    CooperSurgical is recalling Infant Heel Gel Warmers and The Infant Heel Warmer because products without expiration dates have a remote potential for minor burns.

    Product
    CooperSurgical Infant Heel Gel Warmers, P/N 20418 CooperSurgical The Infant Heal Warmer, P/N 2440 To provide gentle heat to increase blood flow and enhance infant blood sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2015·2015-03-25

    Stryker Recalls Triathlon Distal Capture Assembly Due to Weld Disassociation Risk

    Stryker Howmedica Osteonics is recalling 2,030 Triathlon Distal Capture Assemblies because a weld may disassociate, potentially causing the trigger mechanism to become loose or disassociated.

    Product
    Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon Distal Capture Assembly is used when a surgeon elects to use a capture for the distal femoral resection or proximal tibial resection in a Triathlon primary total knee arthroplasty (TKA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1431-2015·2015-03-25

    Rill Foods Recalls Rocky Mountain Chili Spice Soup Seasoning

    Rill Foods is recalling Rocky Mountain Chili Spice Soup Seasoning because the cumin used may be contaminated with peanut protein.

    Product
    The product label reads in part "***ROCKY MOUNTAIN CHILI SPICE Soup Seasoning*** Net Wt. 3.45 oz (98g) *** Rill Foods***"The product is packaged in a clear flexible laminate bag then placed into a tin which has a see through window on the lid. The label is placed over the top.…
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1285-2015·2015-03-25

    GE Healthcare Treadmill T2100 and T2000 Power Cord Recall

    GE Healthcare is recalling T2100 and T2000 treadmills due to a potential safety issue with the power cord assembly.

    Product
    GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. Also Field Replaceable Unit P/Ns 408930-001 Rev E, 408930-002 Rev C. UPDATE: 3-30-2015: T2100 & T2000 Treadmills with power cord…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1238-2015·2015-03-25

    Elekta Precise Treatment Table Recalled for Positioning Error Risk

    Elekta is recalling Precise Treatment Tables because incorrect sensor installation during maintenance can cause undetected positioning errors, potentially leading to clinical mistreatment.

    Product
    Elekta Precise Treatment Table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1281-2015·2015-03-25

    Synthes Thumb Screws Recalled Due to Incorrect Stainless Steel Material

    Synthes, Inc. is recalling 183 thumb screws for orthopedic aiming arms because incorrect raw material was used, which may lead to stress-corrosion cracking.

    Product
    Thumb Screw for the Synthes Recon Locking Aiming Arm for Lateral Entry Femoral Nails-EX (part number 03.010.048) and the Thumb Screw for the Aiming Arm for Titanium Cannulated Tibial Nails-EX (part number 03.010.052). The Recon Locking Aiming Arm for Lateral Entry Femoral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1434-2015·2015-03-25

    Rill Foods Recalls Taneum Canyon Chili Mix Due to Peanut Contamination

    Rill Foods is recalling Taneum Canyon Chili mix because the cumin used may be contaminated with peanut protein.

    Product
    The product label reads in part "***TANEUM CANYON CHILI*** Rill Foods***NET WT. 7.75 OZ.***" The product is packaged in a clear flexible laminate bag and contains smaller packages of spices as well. The label is white with green and black print. Case label is a white sticker…
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1436-2015·2015-03-25

    Tovli Recalls Vegi-Chef Potato Knishes for Undeclared Yellow #5

    Tovli, Inc. is recalling Vegi-Chef Potato Knishes because they contain undeclared Yellow #5, a food dye.

    Product
    Vegi-Chef Potato Knishes retail pack 1 lb. 8 oz. (680g), UPC 046676-91114-1
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1300-2015·2015-03-25

    CooperSurgical Recalls MediChoice Infant Heel Warmers for Burn Risk

    CooperSurgical is recalling MediChoice Infant Heel Warmers because products without expiration dates have a remote potential for minor burns.

    Product
    MediChoice WarmGel Infant Heel Warmer, Item # 1643069911 MediChoice Liquid Infant Heel Warmer, Item # 1643069912 Single Use and Disposable. Distributed by: Owens & Minor. To provide gentle heat to increase blood flow and enhance infant blood sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1450-2015·2015-03-25

    Goya Recalls Kirby Black Beans and Goya Black Bean Soup for Peanut Contamination

    Goya Foods is recalling Kirby Black Beans Creole Seasoning and Goya Black Bean Soup due to possible peanut contamination.

    Product
    Kirby Black Beans Creole Seasoning Net Wt. 29 oz. Packed for Kirby Foods Inc., Miami, Florida 33172 Product of Dominican Republic UPC 0 7738512346 4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1273-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals

    Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes because some packages may have open seals, potentially compromising sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: SafeStep Port Access Kit 22G x 0.75in , SafeStep Port Access Kit 22G x 0.75in with Y-Site, SafeStep Port Access Kit 22G x 1 in , SafeStep Port Access Kit 20G x 0.75in , SafeStep Port Access Kit…
    Category
    Medical Device
    Distribution
    Distributed nationwide