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.

43276–43300 of 50511

  • HighFDA (Devices)·Z-1673-2013·2013-07-17

    Boston Scientific Recalls NephroMax Balloon Catheter Kits Due to Packaging Error

    Boston Scientific is recalling 15 NephroMax high pressure nephrostomy Balloon Catheter Kits because an incorrectly sized renal sheath was packaged with the device.

    Product
    NephroMax high Pressure nephrostomy Balloon Catheter Kit. Material Number/Catalog Number: M0062101600/210-160, M0062101640/210-164 Dilation of the nephrostomy tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1695-2013·2013-07-17

    Biomet Recalls Oxford Fixed Bearing Partial Knee Components Due to Design Flaw

    Biomet is recalling 26 Oxford Fixed Bearing Partial Knee components because the tibial bearing design may cause anterior impingement between bone and the poly bearing.

    Product
    REF 154200 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size A3 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartment Sterile R The Oxford Fixed Bearing Knee is a Partial knee replacement system consisting of a femoral component and a fixed bearing…
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1701-2013·2013-07-17

    Biomet Recalls Oxford Fixed Bearing Partial Knee Components Due to Design Flaw

    Biomet is recalling 24 Oxford Fixed Bearing Partial Knee components due to a design flaw that may cause anterior impingement between bone and the poly bearing.

    Product
    REF 154208 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size B4 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartment Sterile R The Oxford Fixed Bearing Knee is a Partial knee replacement system consisting of a femoral component and a fixed bearing…
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-1599-2013·2013-07-17

    Salmolux Recalls Cold Smoked Salmon for Potential Listeria Contamination

    Salmolux is recalling specific cold smoked salmon products due to potential Listeria monocytogenes contamination. Consumers in ten states should check their refrigerators for these items.

    Product
    ATLANTIC SALMON: 1) "***Raley's***NOVA LOX***NET WT 4 OZ (113 g)***INGREDIENTS: ATLANTIC SALMON (FARM RAISED-COLOR ADDED), SALT, SUGAR, SODIUM NITRITE, NATURAL WOOD SMOKE. CONTAINS: SALMON (FISH)***READY TO EAT***REFRIGERATED BELOW 38F***Proudly Distributed By: Raley's, 500…
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1601-2013·2013-07-17

    Salmolux Recalls Wild Alaskan Nova Lox Smoked Salmon Due to Listeria Risk

    Salmolux is recalling Wild Alaskan Nova Lox Smoked Salmon due to potential Listeria monocytogenes contamination. The product was distributed in ten states.

    Product
    "***WILD ALASKAN NOVA LOX SMOKED SALMON***Sea Passion***INGREDIENTS: Wild Alaskan Salmon, Salt, Sugar, Sodium Nitrite, FD&C Yellow #6, FD&C Red #40 (color enhancers), Natural Wood Smoke. CONTAINS: FISH (SALMON)*** Salmolux Federal Way, WA 98003***0 16468 44543 7***".
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1708-2013·2013-07-17

    Biomet Recalls Oxford Fixed Bearing Partial Knee Components

    Biomet is recalling 24 Oxford Fixed Bearing Partial Knee components due to a design defect that may cause anterior impingement.

    Product
    REF 154217 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size C6 ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartment Sterile R The Oxford Fixed Bearing Knee is a Partial knee replacement system consisting of a femoral component and a fixed bearing…
    Category
    Medical Device
    Distribution
    4 states
  • HighCPSC·13239·2013-07-17

    UCO Arka LED Lanterns Recalled Due to Fire Hazard

    Industrial Revolution is recalling UCO Arka LED lanterns sold at REI because the wall charger plug can fail and cause a fire.

    Product
    UCO Arka LED lanterns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1703-2013·2013-07-17

    Biomet Recalls Oxford Fixed Bearing Partial Knee Components Due to Design Flaw

    Biomet is recalling 22 Oxford Fixed Bearing Partial Knee components because a design flaw creates a potential for anterior impingement between bone and the poly bearing.

    Product
    REF 154210 Oxford Fixed Bearing Partial Knee Cemented Lateral Tibia Size 6ARCOM UHMWPE / CO-CR-MO Alloy Only for use in Lateral compartment Sterile R The Oxford Fixed Bearing Knee is a Partial knee replacement system consisting of a femoral component and a fixed bearing…
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-1641-2013·2013-07-17

    Chs Inc Recalls Contex Textured Soy Protein Due to Salmonella Risk

    Chs Inc is recalling specific batches of Contex textured soy protein produced in Israel due to potential Salmonella contamination. The product was distributed nationwide and to multiple international countries.

    Product
    Contex - Textured Soy Protein Concentrates Item No. / Item Description: 3411112 / Contex 120 Textured Soy Protein, 3411124 / Contex 25 Textured Soy Protein, 3411129 / Contex 31 CL Textured Soy Protein, 3411142 / Contex 120CL IP Textured Soy Protein, 3411144 / Contex 240…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-771-2013·2013-07-17

    Olympia Pharmacy Recalls Phenylbutazone Injection Due to Sterility Concerns

    Olympia Pharmacy is recalling Phenylbutazone 200 mg/ml Injection because FDA inspection findings raised concerns about quality control and sterility assurance.

    Product
    Phenylbutazone 200 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·13V313000·2013-07-16

    Morgan 3W Recall: Missing Brake Fluid Warning Label

    Morgan is recalling 2012-2013 3W motorcycles because the brake fluid reservoir lacks a required filling warning label, which may reduce brake performance.

    Product
    MORGAN — MORGAN 3W
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V311000·2013-07-16

    HL Enterprise Recalls 2013 Trailers Due to Awning Motor Screw Failure

    HL Enterprise is recalling 2013 Hyline, Georgian Bay, Bridgeview, and Premier trailers because power awning motor screws may shear, causing the awning to unfurl unexpectedly.

    Product
    HY-LINE — HY-LINE, BRIDGEVIEW, GEORGIAN BAY HY44, HY42IKEB, BV42IKWT, GB39CKT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V309000·2013-07-15

    Glaval Buses Recalled for Loose Air Conditioner Evaporator Units

    Glaval is recalling certain 2010-2013 buses because the rear air conditioner evaporator may detach from the ceiling, posing an injury risk.

    Product
    GLAVAL BUS — GLAVAL BUS, GLAVAL CONCORDE II, LEGACY, UNIVERSAL, ENTOURAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V301000·2013-07-15

    Lakota Recalls 2014 Charger and Bighorn Trailers for Awning Motor Defect

    Lakota is recalling 2014 Charger and Bighorn recreational trailers because a design change may cause awning motor screws to shear, potentially leading to unexpected awning deployment and injury.

    Product
    LAKOTA — LAKOTA CHARGER, BIGHORN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13742·2013-07-11

    Staples Recalls Bermond Fabric Manager's Chairs Due to Base Breakage

    Staples is recalling Bermond Fabric Manager's Chairs because the base can break, posing a fall hazard. Consumers should stop using the chairs and contact Staples for a refund.

    Product
    Bermond Fabric Manager's Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13236·2013-07-11

    Hollis Recalls Digital Dive Computers Due to Drowning Hazard

    Hollis is recalling DG03 dive computers because a malfunctioning pressure reading could cause divers to deplete their air supply and drown.

    Product
    Hollis DG03 Dive Computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V310000·2013-07-11

    Kawasaki Recalls 2013 EX300 Motorcycles Due to ABS Malfunction

    Kawasaki is recalling 1,083 model year 2013 EX300 motorcycles because a manufacturing error may cause the Anti-Lock Brake System to malfunction, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI EX300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1655-2013·2013-07-10

    HealthLink Biopsy Punches Recalled for Lack of Sterilization

    Clorox Healthcare Holdings is recalling 1,032,700 units of PSS Select Biopsy Punches because they were not sterilized. The products were distributed nationwide and in Canada, Mexico, and New Zealand.

    Product
    PSS Select medical products***Biopsy Punches*** Disposable manual instrument for skin biopsy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V306000·2013-07-10

    Matthews Specialty Vehicles Recalls Buses Due to Awning Motor Screw Shear Risk

    Matthews Specialty Vehicles is recalling specific 2000-2013 model year buses because power awning motor assembly screws may shear, potentially causing the awning to unfurl unexpectedly.

    Product
    THOMAS BUILT — THOMAS BUILT, FREIGHTLINER, INTERNATIONAL CHSU/MICKEY, XCR, FE, TERRASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1646-2013·2013-07-10

    Philips CT Scanners Recalled for Image Artifacts Impairing Diagnostic Quality

    Philips is recalling Brilliance CT 64 and Ingenuity Core scanners due to software issues causing image artifacts that may impair diagnostic quality.

    Product
    Computed Tomography X-ray systems Product Usage: The Brilliance CT 64, Ingenuity Core, and Ingenuity Core128 scanners are whole body Computed Tomography X-ray systems that are intended to produce cross-sectional images of the body by computer reconstruction of x-ray…
    Category
    Medical Device
    Distribution
    Distributed nationwide