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.

33626–33650 of 50502

  • HighFDA (Devices)·Z-0745-2017·2016-12-21

    BD Vacutainer Push Button Blood Collection Set Recall for Barrel Separation

    Becton Dickinson is recalling specific lots of BD Vacutainer Push Button Blood Collection Sets because the front and rear barrels may separate when the safety feature is activated.

    Product
    BD 23 G x .75 in. BD Vacutainer¿ Push Button Blood Collection Set with 12 in. Tubing Catalog # 367342 Intended for venipuncture to obtain blood specimens from patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0760-2017·2016-12-21

    Inovo Purefill Oxygen Compressor Recalled for Operational Failure Risk

    Inovo, Inc. is recalling 117 Inovo Purefill Oxygen Compressor Model PF1100 units because the device can fail during operation.

    Product
    INOVO Purefill Oxygen Compressor Model PF1100 Is an oxygen refill machine that you can attach to an oxygen concentrator to refill portable oxygen cylinders.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0746-2017·2016-12-21

    Steris Recalls Harmony Insight Diagnostic Monitor Support Systems

    Steris Corporation is recalling 63 Harmony Insight Diagnostic Monitor Support Systems because spring arm screws may not be properly secured and could become loose.

    Product
    Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm (EMS) The system is intended for use in surgical operating rooms (OR) or intraoperative surgical/imaging rooms where simultaneous multiple image viewing is required
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0724-2017·2016-12-21

    JFC International Recalls Ramune Candy for Undeclared Wheat Allergen

    JFC International is recalling You-ka Fresh Ramune candy because it may contain undeclared wheat. Consumers with wheat allergies should not consume the product.

    Product
    You-ka Fresh Ramune Net Wt. 3.87oz (110g), Item No. 23925, 20 packs/case
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0737-2017·2016-12-21

    Publix Danish Guava Coffee Cake Recalled for Metal Shavings

    Publix Super Markets is recalling Danish Guava Coffee Cake Strips due to the presence of small metal shavings.

    Product
    Publix Danish Guava Coffee Cake Strip, 15 oz. UPC 002-19562-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0704-2017·2016-12-21

    Cinnabar Specialty Foods Recalls Neera's Spicy Thai Sauce for Undeclared Wheat

    Cinnabar Specialty Foods, Inc. is recalling Neera's Spicy Thai Sauce and Marinade because the product contains undeclared wheat.

    Product
    Neeras Spicy Thai Sauce and Marinade, Net Volume 150ml/5 fl. oz.., 12 units/case, or 6 units/partial case, 2.0 gallon pail.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0736-2017·2016-12-21

    Publix Danish Almond Coffee Cake Recalled for Metal Shavings

    Publix Super Markets is recalling Danish Almond Coffee Cake strips due to the presence of small metal shavings.

    Product
    Publix Danish Almond Coffee Cake Strip, 15 oz. UPC 002-19562-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0765-2017·2016-12-21

    Stryker Recalls Reprocessed Xcel Bladeless Trocars Due to Plug Breakage

    Stryker is recalling 40,476 reprocessed Xcel Bladeless Trocars because the adjustable plug may break in packaging or during use.

    Product
    Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars are indicated for use to establish a port of entry for endoscopic instruments in patients requiring minimally invasive surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0752-2017·2016-12-21

    Integra York Metzenbaum Scissors Recalled Due to Packaging Seal Separation

    Integra York PA, Inc. is recalling 50 units of sterile Metzenbaum Scissors because packaging seals may separate, compromising sterility.

    Product
    Metzenbaum Scissors 7, Curved, Sterile The Metzenbaum Scissors 7, Curved Curved are single-use sterile surgical instruments intended for cutting and grasping tissue in general surgical procedures.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0734-2017·2016-12-21

    Publix Danish Raspberry Coffee Cake Recalled for Metal Shavings

    Publix Super Markets is recalling Danish Raspberry Coffee Cake strips due to the presence of small metal shavings. The product was distributed in six southeastern states.

    Product
    Publix Danish Raspberry Coffee Cake Strip, 15 oz. UPC 002-19562-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0751-2017·2016-12-21

    Integra York Recalls Sterile Rochester-Pean Hemostatic Forceps Due to Seal Defect

    Integra York PA, Inc. is recalling 150 units of sterile Rochester-Pean Hemostatic Forceps because packaging seals may separate, compromising sterility.

    Product
    Rochester-Pean Hemostatic Forceps 61/4, Curved, Sterile. The Rochester-Pean Hemostatic Forceps 61/4 Curved are single-use sterile surgical instruments intended for cutting and grasping tissue in general surgical procedures.
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·16V918000·2016-12-21

    Volvo Recalls 2017 S60, V60, and XC60 for Side Air Bag Defect

    Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflator initiators may fail to ignite during a crash, preventing deployment.

    Product
    VOLVO — VOLVO V60, XC60, S60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0718-2017·2016-12-21

    Clear Spring Foods Recalls Sun-Dried Tomato and Roasted Garlic Trout Fillets

    Clear Spring Foods is recalling Sun-Dried Tomato & Roasted Garlic Trout Fillets due to potential E. coli contamination. The product was distributed in five US states.

    Product
    Label reads in part "***SUN-DRIED TOMATO & ROASTED GARLIC TROUT FILLETS *** Product of USA *** CONTAINS: FISH (TROUT), WHEAT, MILK. *** UPC 10 070765 08761 2 Individual retail packages are mostly green with information panel in white with black lettering. Cases are 10 lbs…
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·16V920000·2016-12-21

    Toyota Recalls 2017 86 Vehicles for Ignition Key Removal Defect

    Toyota is recalling 2017 86 vehicles with automatic transmissions and ignition keys because the key may be removed without the transmission in Park, increasing the risk of the vehicle rolling away.

    Product
    TOYOTA — TOYOTA 86
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0717-2017·2016-12-21

    H-E-B Recalls Baby Pear Peas Zucchini Cups Due to Foreign Object

    H-E-B is recalling specific lots of Baby Pear Peas Zucchini cups because a customer reported finding a small piece of rubber inside the product.

    Product
    HEB Baby Pear Peas Zucchini 4 ounce cups, 2 pack packaged in plastic cups with a cardboard sleeve
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0682-2017·2016-12-21

    Good Sense Trail Mix Recalled for Undeclared Allergens

    Waymouth Farms is recalling Good Sense Trail Mix, Cranberries 'N More, because it may contain undeclared pecans, walnuts, wheat, milk, and soy.

    Product
    Good Sense Trail Mix, Cranberries 'N More, Net Wt. 6 oz. (170g). Cranberries, Sunflower Nuts, Cashews, Pumpkin Seeds, Almonds, Apples. UPC 30243-86343.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-0761-2017·2016-12-21

    Physio-Control Recalls LIFEPAK 15 Monitor/Defibrillators for Unexpected Power Loss

    Physio-Control is recalling 1,399 LIFEPAK 15 monitor/defibrillators because they may power down unexpectedly during use.

    Product
    The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel in outdoor and indoor emergency care settings within the environmental conditions specified. Product Part Numbers V-15-2-000XXX
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0759-2017·2016-12-21

    Telefac Medical Recalls Weck Facial Closure Systems Due to Detachment Risk

    Teleflex Medical is recalling 2,265 units of Weck Facial Closure Systems because the device wings may partially detach from the shield during use.

    Product
    Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision sites.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0764-2017·2016-12-21

    Teleflex Visistat Skin Staplers Recalled for Sterility Deficiency

    Teleflex Medical is recalling Visistat 35W disposable skin staplers because improper packaging seals mean sterility is not assured.

    Product
    WECK Visistat 35W, Disposable Skin Stapler, Rx Only, Sterile, Teleflex Medical, NC 27709. The intended use of the Visistat stapler is to close lacerations on the outer layer of the dermis for a wide range of general, thoracic, obstetric, gynecological, orthopedic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0725-2017·2016-12-21

    JFC International Recalls Fizzy Candy Punch Ramune for Undeclared Wheat

    JFC International is recalling Fizzy Candy Punch Ramune because it may contain undeclared wheat allergen. The recall affects 500 packs distributed in five states.

    Product
    You-ka Punch Ramune Net Wt. 3.87oz (110g), Item No. 23926, 20 packs/case
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0728-2017·2016-12-21

    Prism Medical Carry Bar Recall Due to Breaking Plastic Component

    Prism Medical is recalling carry bars for patient lifts because a black plastic puck may break, posing a risk of harm to patients.

    Product
    Carry bar which is an accessory to a lift used for patients in hospitals and other facilities. Recall impacts the following model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0735-2017·2016-12-21

    Publix Danish Cherry Coffee Cake Recalled for Metal Shavings

    Publix Super Markets is recalling Danish Cherry Coffee Cake strips due to the presence of small metal shavings. The product was distributed in six southeastern states.

    Product
    Publix Danish Cherry Coffee Cake Strip, 15 oz. UPC 002-19562-00000
    Category
    Food
    Distribution
    6 states