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.

37551–37575 of 50506

  • HighNHTSA·15V611000·2015-09-30

    Ford Recalls 2016 F-53 and F-59 Trucks for Shift Cable Defect

    Ford is recalling 2016 F-53 and F-59 stripped chassis trucks because an incorrect shift cable bracket may allow the vehicle to shift out of park without brakes applied.

    Product
    FORD — FORD F-53, F-59
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2791-2015·2015-09-30

    Terumo Cardiovascular Procedure Kits Recalled Due to Defective Hemoconcentrators

    Terumo is recalling 19 custom cardiovascular procedure kits because they contain recalled Medivators HPH700 hemoconcentrators.

    Product
    Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N: 75185 Terumo Cardiovascular Procedure Kits are manufactured and customized to the design and specifications of the purchaser and/or the purchaser's principal technical representative for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2809-2015·2015-09-30

    Beckman Coulter MicroScan LabPro Software Recall for Manual Editing Error

    Beckman Coulter is recalling MicroScan LabPro software versions 1.0 to 4.11 because it incorrectly allows manual editing of carbohydrate substrates during specific manual readings.

    Product
    MicroScan LabPro Information Manager System, Version 1.0 to Version 4.11, Catalog No. 10714149, 10714150. Intended to manage both microbial identification (ID) and antimicrobial agent susceptibility testing (AST).
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-2812-2015·2015-09-30

    Siemens Medical Solutions Recalls Linear Accelerator Systems Due to Collision Risk

    Siemens Medical Solutions is recalling 26 linear accelerator systems and associated software because a defect could cause automatic movement, posing a collision risk to patients.

    Product
    ARTISTE, ONCOR Avantgarde, ONCOR Impression Plus, ONCOR Expression, PRIMUS, PRIMUS Plus, Syngo RT Therapist; therapeutic treatment of cancer Product Usage: The intended use of the SIEMENS branded ARTISTE and ONCOR family of linear accelerator systems is to deliver X-Ray…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2795-2015·2015-09-30

    Brainlab Disposable Reflective Marker Spheres Recalled for Separation Risk

    Brainlab AG is recalling Disposable Reflective Marker Spheres because they may separate at the mid-point seal, posing a risk to patients during image-guided surgery.

    Product
    Disposable Reflective Marker Spheres The Disposable Reflective Marker Spheres used in conjunction with a stereotaxic instrument consisting of a rigid frame with a calibrated guide mechanism for precisely positioning probes or other devices within a patient's brain, spinal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2816-2015·2015-09-30

    Siemens RAPIDPoint 500 Lactate Cartridges Recalled for Sodium Bias

    Siemens is recalling 49 RAPIDPoint 500 Lactate Cartridges due to a negative sodium bias that affects quality control and patient results.

    Product
    Siemens RAPIDPoint 500 Measurement Cartridge Lactate (100) tests Part Number: 10844813 Product Usage: The RAPIDPoint 500 system is designed for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2787-2015·2015-09-30

    Terumo Custom Cardiovascular Procedure Kits Recalled Due to Component Defect

    Terumo is recalling 32 custom cardiovascular procedure kits because they contain recalled Medivators HPH700 hemoconcentrators.

    Product
    Terumo Custom Cardiovascular Procedure Kit X-Coated Adult Pak P/N: 73124 Terumo Cardiovascular Procedure Kits are manufactured and customized to the design and specifications of the purchaser and/or the purchaser's principal technical representative for the application…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2797-2015·2015-09-30

    Bien Air Dental Contra-Angles Recalled for Potential Tool Loosening

    Bien Air Dental SA is recalling specific EVO 15 contra-angles because the dental tool may loosen and be swallowed.

    Product
    Contra-Angles CA1:1L EVO 15 Catalog numbers: 1600939-001 and 1600938-001 Used for generally dentistry procedures
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Drugs)·D-1815-2015·2015-09-30

    Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter

    Hospira, Inc. is recalling Lidocaine Hydrochloride Injection vials because iron oxide particulate matter was found embedded in the glass vial necks.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2789-2015·2015-09-30

    Terumo Custom Cardiovascular Procedure Kits Recalled for Defective Hemoconcentrators

    Terumo is recalling six custom cardiovascular procedure kits nationwide because they contain recalled Medivators HPH700 hemoconcentrators.

    Product
    Terumo Custom Cardiovascular Procedure Kit X-Coated Pediatric Pack P/N: 74039-02 Terumo Cardiovascular Procedure Kits are manufactured and customized to the design and specifications of the purchaser and/or the purchaser's principal technical representative for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2786-2015·2015-09-30

    Terumo Custom Cardiovascular Procedure Kits Recalled for Defective Hemoconcentrators

    Terumo is recalling 5 Custom Cardiovascular Procedure Kits because they contain recalled Medivators HPH700 Hemoconcentrators.

    Product
    Terumo Custom Cardiovascular Procedure Kit Tubing Pack P/N: 66041-1 Terumo Cardiovascular Procedure Kits are manufactured and customized to the design and specifications of the purchaser and/or the purchaser's principal technical representative for the application intended by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2792-2015·2015-09-30

    Terumo Custom Cardiovascular Procedure Kits Recalled Due to Component Defect

    Terumo is recalling 17 custom cardiovascular procedure kits because they contain recalled Medivators HPH700 hemoconcentrators.

    Product
    Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N: 75529 Terumo Cardiovascular Procedure Kits are manufactured and customized to the design and specifications of the purchaser and/or the purchaser's principal technical representative for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2780-2015·2015-09-30

    Edwards Lifesciences Recalls ThruPort Knot Pusher Due to Suture Fraying Risk

    Edwards Lifesciences is recalling 759 ThruPort Knot Pusher units because the device's tip design may cause suture fraying or splitting, potentially compromising suture knot integrity during cardiac surgery.

    Product
    ThruPort Knot Pusher. This device is sold individually (Model KP1) and as part of the ThruPort Valve Placement Pack (Model VPP). packaged sterile and non-pyrogenic in a sealed, peel-type pouch. The Knot Pusher is a sterile disposable plastic rod used to advance extracorporeal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2793-2015·2015-09-30

    Ecolab Recalls Microtek ORS Fluid Warming and Slush Drapes Due to Seal Defects

    Ecolab is recalling Microtek ORS Fluid Warming and Slush Drapes because sterile packaging seals may contain small channels, potentially compromising package integrity and sterility.

    Product
    Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-100, ORS-110, ORS-130, ORS-300, ORS-301, ORS-320, ORS-321, ORS-325, ORS-330, ORS-331 and ORS-2200. The ORS Fluid Warming and Slush Drapes are individually wrapped and placed in poly-Tyvek pouches with…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-3242-2015·2015-09-30

    Hillside Quickie Too Recalls Seitan Steak Sandwiches for Allergen Mislabeling

    Hillside Quickie Too is recalling Seitan Steak sandwiches because the wheat bun was not listed in the 'Contains' statement, posing a risk to consumers with wheat allergies.

    Product
    Seitan Steak is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Category
    Food
    Distribution
    1 state
  • HighCPSC·15255·2015-09-29

    Chewbeads Recalls Pacifier Clips Due to Choking Hazard

    Chewbeads is recalling approximately 45,000 pacifier clips in the U.S. because the D-ring can break, allowing beads to detach and pose a choking hazard.

    Product
    Pacifier clips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15253·2015-09-29

    Bicycles with Front Disc Brakes Recalled for Crash Hazard

    Thirteen manufacturers recall about 1.3 million bicycles with front disc brakes and quick-release levers due to a crash hazard. Consumers should stop using the bikes and contact the manufacturer for a free replacement.

    Product
    Bicycles equipped with front disc brakes and quick release levers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15256·2015-09-29

    Calphalon Recalls Pizza Wheels Due to Handle Detachment and Laceration Risk

    Calphalon is recalling pizza wheels because the handle can detach during use, posing a laceration hazard. Consumers should stop using the product and contact the company for a refund.

    Product
    Pizza wheel pizza cutters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15254·2015-09-29

    Madewell Recalls Katya Sandals Due to Metal Shank Fall Hazard

    Madewell is recalling Katya sandals because a metal shank can dislodge and break through the outsole, posing a fall hazard. No injuries have been reported.

    Product
    Sandals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15257·2015-09-29

    Ross Stores Recalls Rattan Arm Chairs Due to Fall Hazard

    Ross Stores is recalling rattan arm chairs because they may tip or slide backward, posing a fall hazard. Eight reports of minor injuries have been received.

    Product
    Rattan Arm Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V601000·2015-09-25

    Merhow Recalls Horse Trailers Due to Door Lock Jamming Risk

    Merhow is recalling 2006-2013 Horse Trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    MERHOW — MERHOW HORSE TRAIELRS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·125-2015·2015-09-25

    Calperf Recalls Marinated Chicken Product Due to Undeclared Milk Allergen

    Calperf is recalling approximately 216 pounds of marinated chicken product because it contains milk, a known allergen, that is not declared on the ingredient list.

    Product
    CREATIVE FOOD PROCESSING — Calperf Recalls Chicken Product Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    1 state