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.

24001–24025 of 50435

  • HighFDA (Devices)·Z-0918-2020·2020-02-05

    ROi CPS Recalls Custom Procedure Packs Containing Recalled Clearlink Devices

    ROi CPS LLC is recalling 412 custom procedure packs containing Clearlink Continu-Flo devices that were previously recalled by Baxter Healthcare Corporation.

    Product
    Custom procedure packs, containing Clearlink Continu-Flo, labeled as follows: a) regard LD00200L-VAG DELIVERY MOTHER - JOPLIN, Item Number 830015012 b) regard GS00310C - Max Barrier Central Line Trpl Lumen 16cm, Sulfa-coated catheter, Item Number: 830027 c) regard GS00309B…
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0917-2020·2020-02-05

    Bard Conquest 40 PTA Dilation Catheter Recalled for Packaging Error

    Bard Peripheral Vascular Inc. is recalling 286 units of Conquest 40 PTA Dilation Catheters because packaging incorrectly listed the balloon size, posing a risk of vessel injury.

    Product
    Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire .035"; Recommended Introducer 6F; Nominal Pressure 8atm, Rated Burst Pressure 40atm; Syringe inflation 1cc; UDI: (01)00801741060533(17)220228(10)REDQ3444
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Devices)·Z-0891-2020·2020-02-05

    Haemonetics Recalls Cell Saver 5/5+ Bowl Kits Due to Leak Risk

    Haemonetics is recalling Cell Saver 5/5+ Bowl Kits because they may leak, trapping fluid and causing incomplete washing.

    Product
    Cell Saver¿5/5+ Bowl Kit (225 ml) Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0871-2020·2020-02-05

    Zimmer Biomet Recalls ASI 2.0 Calcar Trimmer Shafts Due to Mating Failure

    Zimmer Biomet is recalling 67 units of ASI 2.0 Calcar Trimmer Shafts because the shaft end may fail to mate effectively with the broach.

    Product
    ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0901-2020·2020-02-05

    Haemonetics Recalls Cell Saver Bowl Sets Due to Potential Leaks

    Haemonetics is recalling Cell Saver bowl sets because cracks may cause leaks and incomplete blood washing.

    Product
    Japan CS Elite FASTPACK DISP. SET - 125ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0573-2020·2020-02-05

    Kindroot Adaptogems Lozenges Recalled for Undeclared Fish Allergen

    Kindroot LLC is recalling Peach Blossom plant lozenges because the label failed to list fish as the source of collagen peptides.

    Product
    kindroot adaptogems; Peach Blossom Plant lozenges for lit looks. 20 lozenges net wt. 2.6 oz. 74 g - Dietary Supplement UPC: 8 60000 30544 0 Ingredients: Marine collagen Peptides, Ashwagandha Root Extract (organic). Other ingredients: Organic Brown Rice Syrup, malic…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0847-2020·2020-02-05

    Vitreq 25G Blunt and Brush Needles Recalled for Sterility Risk

    Vitreq Bv is recalling VitreQ 25G Blunt and Brush Needles because microscopic tears in the sterile pouch may compromise sterility.

    Product
    (1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G BF Brush Needles-BF25.D52 GTIN: 8719214221188
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20T002000·2020-02-04

    Goodyear Recalls Fortera HL Tires Due to Belt Separation Risk

    Goodyear is recalling specific Fortera HL tires because a manufacturing issue may cause belt separation, increasing the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V054000·2020-01-31

    Triple E Recalls 2020 Motorhomes Due to Propane Line Defects

    Triple E is recalling 237 2020 Unity, Wonder, and Serenity motorhomes because twisted or kinked propane lines may leak and cause a fire.

    Product
    WONDER — WONDER, UNITY, SERENITY W24RTB, W24MB, W24FTB, U24MB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V057000·2020-01-31

    Volkswagen Recalls 2018 Atlas Vehicles Due to Air Bag Sensor Defect

    Volkswagen is recalling 2018 Atlas vehicles because an incorrectly manufactured air bag sensor may delay or disable deployment, increasing injury risk in crashes.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20716·2020-01-30

    K-Apparel Recalls Children's Lounge Pants Due to Burn Hazard

    K-Apparel is recalling about 2,200 TINFL children's lounge pants because they fail federal flammability standards, posing a burn risk to children.

    Product
    Children's Lounge Pants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20714·2020-01-30

    Polaris Recalls 2019 Pro XD Utility Vehicles Due to Rear Brake Failure Risk

    Polaris is recalling about 760 Model Year 2019 Pro XD utility vehicles because the rear brake line can puncture, causing rear brake failure and posing a crash hazard.

    Product
    Model Year 2019 Polaris PRO XD Utility Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20713·2020-01-30

    Polaris Recalls 2017-2018 Brutus UTVs Due to Rear Brake Line Failure

    Polaris is recalling 2017-2018 Brutus utility vehicles because a rear brake line can puncture, causing brake failure and a crash hazard.

    Product
    Model Year 2017-2018 Brutus Utility Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0527-2020·2020-01-29

    Pike Place Smoked Salmon Chowder Recalled for Gluten Mislabeling

    Northwest Gourmet Food Products Inc. is recalling Pike Place Smoked Salmon Chowder because the outer packaging claims 'Gluten Free' while the inner pouch declares wheat.

    Product
    Smoked Salmon Chowder, Pike Place Chowder brand, item #89201, distributed By PPC Trading Co. M. BOX #262 4580 Klahanie Drive SE Issaquah WA 98029. There are 16/16 oz. retail packages per master case. Retail package net wt. 16 oz. UPC 8 56112 00406 7. The 16 oz. inner…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0830-2020·2020-01-29

    Siemens ADVIA Centaur Folate Test Kits Recalled for Potential Interference

    Siemens is recalling ADVIA Centaur Folate test kits because homocysteine assays may cause elevated folate results.

    Product
    Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate in serum or red blood cells SMN: 10325366
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0530-2020·2020-01-29

    ASK Foods Recalls Jonah Crab Meat Stuffing Due to Listeria

    ASK Foods Inc is recalling Jonah Crab Meat Stuffing because the cheese ingredient tested positive for Listeria monocytogenes.

    Product
    Jonah Crab Meat Stuffing 5 lb. (2.27 kg) Bulk Plastic Container,6 - 5 lb. containers per case , Keep Frozen
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0823-2020·2020-01-29

    Isopure Centrifugal Pump Recall Due to Magnet Encapsulation Defect

    Isopure Corp is recalling eight Finish Thompson Centrifugal Pumps due to a manufacturing defect that could expose magnets to solution, causing corrosion and iron contamination.

    Product
    Finish Thompson Centrifugal Pump Model #110192-3 (sold as spare part)
    Category
    Medical Device
    Distribution
    13 states