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.

36651–36675 of 50504

  • HighFDA (Food)·F-0376-2016·2016-02-17

    Kraft Singles Deli Deluxe American Slices Recalled for Choking Hazard

    Kraft Heinz is recalling specific lots of Kraft Singles Deli Deluxe American Slices because packaging film may remain on the cheese, posing a choking risk.

    Product
    Kraft Singles Deli Deluxe American Slices packaged in a blue box with white lettering.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0789-2016·2016-02-17

    Richard Wolf Reusable Rotary Blade Recall Due to Weak Welds

    Richard Wolf Medical Instruments Corp. is recalling ten reusable rotary blade/abrader units due to weak welds that may cause the product to break during surgical use.

    Product
    Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0561-2016·2016-02-17

    Albertsons Recalls Coast to Coast Sourdough Hoagie Rolls Due to Foreign Material

    Albertsons Companies, Inc. is recalling Coast to Coast San Francisco Style Sourdough 6 Hoagie Rolls because cloth material from production equipment may be present in the product.

    Product
    Coast to Coast San Francisco Style Sourdough 6 Hoagie Rolls; 6 Hoagie Rolls; NET WT 16.5 oz 468 g UPC 0 21130 18091 2; Distributed by Living Better Brands, LLC, Pleasanton, CA 94566 Contains: Wheat May Contain eggs, milk.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0549-2016·2016-02-17

    Zingerman's Candy Bars Recalled for Undeclared Soy and Milk Allergens

    Zingerman's Candy Manufactory is recalling Zzang! Holiday 4 pack Candy Bars due to undeclared soy and milk allergens.

    Product
    Zzang! Holiday 4 pack Candy Bars, 10.5 oz., packaged in preprinted cardboard boxes
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0688-2016·2016-02-17

    Moog Recalls Curlin Infusion Pumps Due to Calibration Defect

    Moog is recalling specific Curlin infusion pumps because calibration errors may cause them to deliver medication faster than programmed.

    Product
    Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000, catalog number 340; Curlin 6000, 6000 CMS, and PainSmart IOD, catalog number 360; and Curlin Pump Calibration Set…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0374-2016·2016-02-17

    Kraft Singles American Recalled for Potential Choking Hazard

    The Kraft Heinz Company is recalling Kraft Singles American cheese slices because thin strips of packaging film may remain on the slices, posing a potential choking hazard.

    Product
    Kraft Singles American packaged in a blue box with white lettering.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0787-2016·2016-02-17

    DePuy SIGMA HP MBT Non-Keel Punch Knee Instrument Recalled

    DePuy Orthopaedics is recalling 351 SIGMA HP MBT Non-Keel Punch Knee Instruments due to a design defect that may cause surgical complications.

    Product
    SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be used as an option in stabilizing the tibial trial during trial reduction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0759-2016·2016-02-17

    Trumpf Medical Systems Recalls Patient Transport Shuttles Due to Tilting Hazard

    Trumpf Medical Systems is recalling 1,284 patient transport shuttles because the table top may tilt down quickly in the maximum Trendelenburg position.

    Product
    Patient transport Shuttle with Trendelenburg quick adjustment function (Jupiter, Mars, Titan, TruSystem and Saturn operating table systems). The shuttle is intended for the following applications: 1. Transfer, transport and storage of exchangeable table tops in the Trumpf…
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·16V090000·2016-02-17

    Navistar Recalls 2016 IC CE Buses for Hood Strap Defect

    Navistar is recalling 104 model year 2016 IC CE commercial buses because hood straps may elongate, causing the hood to open unexpectedly during braking and obstructing the driver's vision.

    Product
    IC BUS — IC BUS CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2016·2016-02-17

    GE Healthcare Optima XR220amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 2,389 Optima XR220amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.

    Product
    GE Healthcare, Optima XR220amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-0565-2016·2016-02-17

    Celestial Seasonings Roastaroma Herbal Tea Recalled for Gluten Mislabeling

    Hain Celestial is recalling Roastaroma Herbal Tea because some packages are labeled 'Gluten Free' but contain barley.

    Product
    Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17 Pack size: 6 retail units (20 count)/ per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0769-2016·2016-02-17

    GE Brivo XR285amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 126 Brivo XR285amx mobile radiographic systems worldwide because a safety latch mechanism may fail, posing a risk of bodily harm.

    Product
    GE Healthcare, Brivo XR285amx Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0792-2016·2016-02-17

    Mizuho OSI Trios Table Base Recall for Missing Retaining Ring

    Mizuho OSI is recalling 33 Trios table bases because a missing retaining ring may cause the clutch to jam, preventing patient rotation.

    Product
    Mizuho OSI Trios, Table Base; Voltage: 100-240V ~ 50/60 Hz Amps: 5,0-5.0A; Model 7803 and 7803AP Orthopaedic: Operating room tablebase - an electronically powered mobile operating table is created, designed for temporary (<24 hours) support and positioning of a patient in…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0550-2016·2016-02-17

    Zingerman's Recalls Chocolate Marshmallows Due to Undeclared Soy

    Zingerman's Candy Manufactory is recalling 8-ounce bags of Chocolate Marshmallows because they contain undeclared soy. The recall affects 134 units distributed across 18 states and Washington, D.C.

    Product
    Chocolate Marshmallows, 8 oz., packaged in plastic bags, UPC 8 44397 00077 5
    Category
    Food
    Distribution
    18 states
  • HighCPSC·16103·2016-02-17

    Michaels Recalls Artificial Poinsettias Due to Mold Exposure Risk

    Michaels is recalling Ashland artificial poinsettia stems and bushes because mold may be present, posing a risk of respiratory or other infections.

    Product
    Ashland Poinsettia Stems and Bushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0790-2016·2016-02-17

    Richard Wolf Reusable Rotary Blade Recalled for Weak Welds

    Richard Wolf Medical Instruments Corp. is recalling four reusable rotary blade/abrader units due to weak welds that may cause the product to break during surgical use.

    Product
    Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0788-2016·2016-02-17

    Zimmer Biomet Recalls Endobon Xenograft Granules Due to Cytotoxicity Failure

    Biomet France SARL is recalling Endobon-Xenograft Granules because the product failed cytotoxicity tests at 36 months. Use past the 18-month shelf life may cause patient illness or injury.

    Product
    Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures. Endobon Xenograft Granules, Bone Grafting Material, Synthetic are used in the following dental and/or surgical procedures: " Alveolar ridge…
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Devices)·Z-0770-2016·2016-02-17

    GE Healthcare Optima XR200amx Mobile Radiographic System Recalled for Safety Latch Failure

    GE Medical Systems is recalling 895 Optima XR200amx mobile radiographic systems worldwide due to a potential safety latch mechanism failure that could cause the arm assembly to fall.

    Product
    GE Healthcare, Optima XR200amx, Mobile Digital Ready Radiographic System Designed to generate diagnostic radiographic images.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-0546-2016·2016-02-17

    Zzang! Original Candy Bar Recalled for Undeclared Soy and Milk

    Zingerman's Candy Manufactory is recalling Zzang! Original Candy Bars due to undeclared soy and milk allergens.

    Product
    Zzang! Original Candy Bar, 2.5 oz., packaged in preprinted cardboard boxes, UPC 8 44397 00014 0
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0548-2016·2016-02-17

    Zingerman's Wowza Candy Bar Recalled for Undeclared Soy and Milk

    Zingerman's Candy Manufactory is recalling 1,499 Wowza Candy Bars due to undeclared soy and milk ingredients.

    Product
    Zzang! Wowza Candy Bar,3 oz., packaged in reprinted cardboard boxes, UPC 8 44397 00072 0
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0764-2016·2016-02-17

    Philips Allura Xper FD20 Ceiling Version Recalled for C-Arc Movement

    Philips is recalling 15 Allura Xper FD20 Ceiling version units because improper adjustment may cause the C-arc to continue moving after stopping.

    Product
    Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·16V089000·2016-02-17

    Keystone Recalls 2016 Sprinter RVs Due to Falling Television Risk

    Keystone is recalling 2016 Sprinter recreational vehicles because a wall-mounted television may break off, posing an injury risk to occupants.

    Product
    KEYSTONE — KEYSTONE SPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0547-2016·2016-02-17

    Zzang! Cashew Cow Candy Bar Recalled for Undeclared Soy

    Zingerman's Candy Manufactory is recalling Zzang! Cashew Cow Candy Bars due to undeclared soy. The product was distributed in 18 states and DC.

    Product
    Zzang! Cashew Cow Candy Bar,2 oz., packaged in reprinted cardboard boxes, UPC 8 44397 00015 7
    Category
    Food
    Distribution
    18 states
  • HighFDA (Drugs)·D-0655-2016·2016-02-17

    Fagron Recalls SyrSpend SF Grape Flavor Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF Grape Flavor suspending base due to the presence of yeast. The recall affects 148 bottles distributed nationwide.

    Product
    SyrSpend SF, Suspending Base, Grape Flavored, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·16104·2016-02-17

    Michaels Recalls Ashland Holiday Paper Boxes Due to Mold Risk

    Michaels is recalling Ashland holiday paper boxes because mold may be present, posing a risk of respiratory or other infections for consumers with compromised immune systems or mold allergies.

    Product
    Ashland® holiday paper boxes
    Category
    Consumer Product
    Distribution
    Distributed nationwide