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.

20726–20750 of 50413

  • HighFDA (Devices)·Z-1342-2021·2021-04-07

    Diasorin Recalls LIAISON 1-84 PTH Assay Due to Falsely Elevated Results

    Diasorin Inc. is recalling LIAISON 1-84 PTH Assay kits because the system may produce falsely elevated parathyroid hormone results.

    Product
    LIAISON 1-84 PTH Assay - Product Usage: is an in vitro chemiluminescent immunoassay (CLIA) intended for the quantitative determination of parathyroid hormone (1-84) in human serum and EDTA plasma. Measurements of parathyroid hormone levels are used in the differential diagnosis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0374-2021·2021-04-07

    J & J Distributing Recalls Tastebuds Taco Dip for Listeria Risk

    J & J Distributing Company is recalling 371 units of Tastebuds Taco Dip due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    tastebuds Taco Dip, Net Wt. 9oz (255g), UPC 0 38232 31612 5, Distributed By H. Brooks & Co Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1325-2021·2021-04-07

    Nuvasive Recalls PRECICE Plates Due to Biological Safety Concerns

    Nuvasive Specialized Orthopedics Inc is recalling 40 PRECICE Plate units worldwide due to complaints of adverse events potentially related to biological safety.

    Product
    PRECICE PLATE - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1319-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 15 DiamondTemp Bidirectional Small Curve Ablation Catheters because the packaging and instructions for use list incorrect catheter sizes.

    Product
    EPIX Therapeutics DiamondTemp Bidrectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:CEDTB300S, SterileEO, UDI: 00812499030358
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0376-2021·2021-04-07

    AMPI Buttermilk Powder Recalled for Potential Metal Contamination

    AMPI is recalling 621 bags of Buttermilk Powder, formula 219, due to the potential presence of foreign material (metal). The product was distributed in Wisconsin.

    Product
    AMPI Buttermilk Powder, formula 219. 25 KG Net (55.12 Lbs Net). Distributed by: Associated Milk Producers, Inc., New Ulm, Minnesota 56073. Packaged in Kraft Paper Poly-lined bags.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1333-2021·2021-04-07

    Biocare Medical IntelliPath FLX Automated Staining Instrument Recall

    Biocare Medical is recalling 72 IntelliPath FLX instruments due to a software defect that may cause random movement and buffer dispensing errors.

    Product
    BIOCARE Medical , IntelliPath FLX, Automated Staining Instrument, Ref: " Model Number:IPS0001US and IPS0001INTL containing software version 3.5.3.1
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Food)·F-0368-2021·2021-04-07

    J & J Distributing Recalls Taco Platter Due to Listeria Risk

    J & J Distributing Company is recalling Taco Platters sold at Kwik Trip locations due to potential Listeria monocytogenes contamination.

    Product
    Taco Platter [Kwik Trip], Net Wt. 15.8oz (448g), UPC 0 38232 36090 6, Distributed By H. Brooks & Co. Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1311-2021·2021-04-07

    Hollister Recalls Vertical Drain Tube Attachment Devices Due to Separation Risk

    Hollister Incorporated is recalling Vertical Drain Tube Attachment Devices (VTAD) because the tube holder can separate from the securing barrier, risking tube migration or loss.

    Product
    Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to stabilize and secure a variety of catheters, surgical drains, and tubes from sizes 5-40 French.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1321-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 19 DiamondTemp Unidirectional Ablation Catheters because packaging and instructions list incorrect sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Small Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT100S,SterileEO, Rx Only, UDI: 00812499030006
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0367-2021·2021-04-07

    J & J Distributing Recalls Tastebuds Layered Fiesta Taco Dip for Listeria Risk

    J & J Distributing Company is recalling Tastebuds Layered Fiesta Taco Dip due to potential Listeria monocytogenes contamination. The product was distributed to 46 retail locations in eight states.

    Product
    tastebuds Layered Fiesta Taco Dip, Net Wt. 9 oz. (255g), UPC 0 38232 31611 8, Distributed By H. Brooks & Co Mpls MN 55112
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-0366-2021·2021-04-07

    Haug Fresh Taco Tray Recalled for Listeria Monocytogenes Contamination

    J & J Distributing Company is recalling Haug Fresh Taco Tray products due to potential contamination with Listeria monocytogenes.

    Product
    Haug Fresh Taco Tray, Net Wt. 29 oz. (823g), UPC 6 10014 16416 4; Net Wt. 16 oz (454g), UPC 6 10014 16383 9; Net Wt. 16 oz (454g), UPC 6 10014 16415 7, 2/16 oz packages per unit. Packed & Distributed by J&J Distributing, 653 Rice St. St. Paul, MN 55103.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1322-2021·2021-04-07

    EPIX Therapeutics DiamondTemp Catheter Recalled for Labeling Errors

    EPIX Therapeutics is recalling 13 DiamondTemp Unidirectional Ablation Catheters because packaging and instructions list incorrect sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Large Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT200L, SterileEO, Rx Only, UDI: 00812499030013
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0318-2021·2021-04-07

    Ferring Recalls ZOMA-Jet 10 Demonstration Kits Due to Defective Delivery System

    Ferring Pharmaceuticals is recalling 1,569 ZOMA-Jet 10 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.

    Product
    ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial, ZOMA-Jet 10 Demonstration Kit contains -ZOMA-Jet 10 device - 7 Needle-Free Head A's - 1 Carrying Case - 1 User Manual; Manufactured for: Ferring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V241000·2021-04-06

    Mercedes-Benz and Freightliner Sprinter Recalled for Steering Hose Defect

    Daimler Vans USA is recalling 2019-2020 Sprinter vans because hydraulic power steering hoses may detach, causing fluid leaks and loss of steering assist.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER (VS30), SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V242000·2021-04-06

    Arcimoto Electric Motorcycles Recalled for Inverter Firmware Defect

    Arcimoto is recalling 2019-2021 FUV, 2020-2021 Deliverator and Roadster, and 2021 Rapid Responder motorcycles. A firmware defect in the inverter may cause the vehicle's battery to shutdown without warning, increasing the risk of a crash.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V236000·2021-04-05

    2021 Forest River Flagstaff and Rockwood Fifth Wheels Pin Box Defect

    Forest River is recalling certain 2021 Flagstaff and Rockwood fifth wheels due to pin box defects. The pin box may be under-rated for the vehicle's gross weight rating, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V234000·2021-04-04

    2021 INFINITI Q50 and Q60 Engine Control Module Software Defect

    INFINITI is recalling 2021 Q50 and Q60 vehicles for an Engine Control Module software defect that may cause engine stall and increase crash risk. Dealers will reprogram the ECM software free of charge.

    Product
    INFINITI — INFINITI Q50, Q60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21735·2021-04-01

    BATTOP Foldable Infant Bath Seats Recalled for Drowning Hazard

    BATTOP is recalling about 5,000 foldable infant bath seats sold on Amazon.com because they can tip over, posing a drowning risk to babies.

    Product
    Foldable Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21734·2021-04-01

    doTERRA Recalls Essential Oils Due to Non-Child-Resistant Packaging

    doTERRA is recalling 1.3 million bottles of Deep Blue, PastTense, and Deep Blue Touch essential oils because the packaging is not child-resistant, posing a poisoning risk.

    Product
    doTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V233000·2021-04-01

    Mack heavy trucks recalled for electronic stability control software malfunction

    Mack trucks (2018-2022) with electronic stability control may drift out of their lane at certain speeds, increasing crash risk. Dealers will reprogram the control units free of charge.

    Product
    MACK — MACK GRANITE (GR), GRANITE (GU), PINNACLE (CXU), PINNACLE (CHU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V230000·2021-04-01

    2021 Mercedes-Benz Vehicles Recalled for Faulty Seat Switch

    2021 Mercedes-Benz vehicles are being recalled due to a faulty seat position switch that may prevent airbags and seatbelt force limiters from activating during a crash. MBUSA will replace the switches free of charge.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450, C 300, E 350, AMG GT63S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V231000·2021-04-01

    2021 Mercedes-Benz GLB vehicles recalled for potentially detaching tailgate spoilers

    Mercedes-Benz is recalling certain 2021 GLB35 AMG and 2020–2021 GLB250 vehicles because the side spoilers on the tailgate might not have been installed correctly, allowing them to detach and create a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250, AMG GLB35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V226000·2021-04-01

    2021 International RH and LT Vehicles Parking Brake Defect

    Certain 2021 International RH and LT vehicles have a defective spring brake chamber that may allow the parking brake to malfunction, increasing crash risk. Navistar will replace the defective brake chambers at no cost.

    Product
    INTERNATIONAL — INTERNATIONAL RH, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide