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.

45076–45100 of 50512

  • HighFDA (Food)·F-2038-2012·2012-09-05

    Cass-Clay Creamery Recalls Ice Cream for Undeclared Soy and Wheat

    Cass-Clay Creamery is voluntarily recalling specific ice cream products because they may contain undeclared soy lecithin and wheat.

    Product
    CASS-CLAY: LIGHT DUSTY ROAD, ONE GALLON (3.78 L), 0 70422 23480 2. LIGHT ICE CREAM, DUSTY ROAD, HALF GALLON (1.89L), 0 70422 24080 3
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2267-2012·2012-09-05

    Metrex Recalls CaviCide Disinfectant Due to Reported Health Reactions

    Metrex Research is recalling CaviCide disinfectant with Spring Fresh Fragrance because it caused health reactions like headaches and nausea in some users.

    Product
    CaviCide, Part Numbers: 13-1025, 13-1000, 13-1024, MC-1000. Alternate brands: EnviroCide, part number: 13-3325. Private labeled products of Cavicide: Backscratchers Cavicide, part number: 13-4800. MaxiSpray Plus, part numbers: 13-7400 and 13-7405. pdCARE Surface…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2039-2012·2012-09-05

    Cass Clay Creamery Recalls Ice Cream for Labeling Errors

    Cass Clay Creamery is voluntarily recalling 23,852 containers of light French vanilla ice cream due to non-compliant egg labeling and undeclared Yellow 5 color.

    Product
    HORNBACHERS, LIGHT FRENCH VANILLA, HALF GALLON (1.89L), 0 41130 21662 6 (Missing Egg from Contains statement) SUNNYBROOK, LIGHT FRENCH VANILLA, HALF GALLON (1.89 L), 0 70422 24917 2 . (MISSING YELLOW 5 FROM LABEL) DAN'S, LIGHT FRENCH VANILLA, HALF GALLON(1.89 L), 0…
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2061-2012·2012-09-05

    Cass-Clay Ice Cream Recalled for Undeclared Soy Lecithin

    Cass-Clay Creamery is voluntarily recalling specific ice cream products because they may contain undeclared soy lecithin, a common allergen.

    Product
    Cass-Clay, COOKIES 'N VANILLA 3 Gallon (11.34 L)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2290-2012·2012-09-05

    Unimed Recalls Medline Electrosurgical Needles Due to Sterility Concerns

    Unimed Surgical Products is recalling Medline electrosurgical needles due to concerns about sterility. The affected lot is distributed nationwide.

    Product
    Product is labeled in part: "***MEDLINE***Staight Microsurgical Needle 3cm (1.81) Length***Reorder: ESE1651***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2036-2012·2012-09-05

    Cass-Clay Ice Cream Recalled for Undeclared Soy and Peanut Allergens

    Cass-Clay Creamery is voluntarily recalling Double Chocolate Fudge Premium Light Ice Cream because it may contain undeclared soy lecithin and peanut oil.

    Product
    CASS-CLAY, DOUBLE CHOCOLATE FUDGE, Premium Light Ice Cream, HALF GALLON (1.89L), 0 70422 24061 2
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-2057-2012·2012-09-05

    Cass-Clay Creamery Recalls Swiss Chip Ice Cream for Undeclared Soy

    Cass-Clay Creamery is voluntarily recalling Swiss Chip ice cream because it may contain undeclared soy lecithin. The recall affects 81 containers distributed in five states.

    Product
    Cass-Clay , Swiss Chip, 3 Gallon(11.34 L).
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2288-2012·2012-09-05

    Unimed Recalls Medline Electrosurgical Electrodes Due to Sterility Concerns

    Unimed Surgical Products is recalling specific lots of Medline electrosurgical electrodes due to concerns regarding sterility.

    Product
    Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle with Extended Insulation 4.0" (10.16cm) Length***Reorder: ES0016AM***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2263-2012·2012-09-05

    Cisco HealthPresence Software Recall for Vital Signs Display Errors

    Cisco Systems is recalling HealthPresence software version 2.1 because subsequent vital signs readings may not update correctly in the OnePlace tab, potentially leading to incorrect interpretations.

    Product
    Cisco brand HealthPresence, version 2.1; Model/Catalog Number: CHP-ENTPRSYR2.I-K9; Product is manufactured and distributed by Cisco Systems, Inc. San Jose, CA Cisco HealthPresence, version 2 is intended for remote consultation of patients with a healthcare provider. Cisco…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2054-2012·2012-09-05

    Cass Clay Ice Cream Recalled for Undeclared Soy Lecithin

    Cass Clay Creamery is voluntarily recalling Winter Wonder ice cream products because they may contain undeclared soy lecithin.

    Product
    Cass Clay, WINTER WONDER, half gallon (1.89 L) , 0 70422 00100 8 Cass Clay, Winter Wonder, 3 Gallon (11.334 L)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2286-2012·2012-09-05

    Medline Extended PTFE Needle Recall for Sterility Concerns

    Unimed Surgical Products is recalling Medline Extended PTFE Needles due to sterility concerns. The recall affects 1,440 units distributed nationwide.

    Product
    Product is labeled in part: "***MEDLINE***Extended PTFE Needle 6.5" (16.51cm) Length***Reorder: ES0016***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2265-2012·2012-09-05

    Canon Solid State X-ray Imager Recall Due to Loose Screws

    Canon is recalling 468 Solid State X-ray Imagers because screws holding the 55REF circuit board are loosening and roaming inside the sealed sensor.

    Product
    Canon Solid State X-ray Imager (Flat Panel/Digital Imager), Digital Radiography, Models CXDI-55C, CXDI-55G and CXDI-70C. These devices are intended to replace radiographic film/screen systems in all general purpose diagnostic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2292-2012·2012-09-05

    Unimed Recalls Medline Electrosurgical Electrodes Due to Sterility Concerns

    Unimed Surgical Products is recalling Medline electrosurgical electrodes due to concerns about sterility. The recall affects 1,920 units distributed nationwide.

    Product
    Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade 6.5 (16.51cm) Length***Reorder: ES0014***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2093-2012·2012-09-05

    Shin Shin Foods Recalls Strawberry Yogurt Parfait for Undeclared Coconut

    Shin Shin Foods is recalling Strawberry Yogurt Parfait because it contains coconut, which is not declared on the label.

    Product
    Yogurt Parfait Strawberry, Net weight 9 oz. (225 g), UPC 0 20728 70004 4. Product contains yogurt and strawberry filling and one cup of granola, packaged in a clear container, and granola is in the inner container. The product is labeled in part: '***YOGURT PARFAIT…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2291-2012·2012-09-05

    Unimed Recalls Medline Electrosurgical Electrodes Due to Sterility Concerns

    Unimed Surgical Products is recalling specific lots of Medline electrosurgical electrodes due to concerns regarding sterility.

    Product
    Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle with Extended Insulation 2.75 (6.99cm) Length***Reorder: ES0013M***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2053-2012·2012-09-05

    Cass Clay Ice Cream Recalled for Undeclared Soy Allergen

    Cass Clay Creamery is voluntarily recalling specific ice cream products because they may contain undeclared soy lecithin.

    Product
    Cass Clay, PEPPERMINT CANDY, half gallon (1.89 L), 0 70422 00100 8 Cass Clay, Peppermint Stic, 3 Gallon (11.34 L).
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·12V432000·2012-09-05

    Honda Recalls 2012 Ridgeline Vehicles Due to Airbag Indicator Defect

    Honda is recalling specific 2012 Ridgeline vehicles because an incorrect passenger airbag status indicator may be installed. This could prevent drivers from knowing the front passenger airbag is off.

    Product
    HONDA — HONDA RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2279-2012·2012-09-05

    Mindray Recalls V Series Patient Monitors Due to Software Anomalies

    Mindray is recalling 979 V Series Patient Monitors worldwide due to two identified software anomalies. No injuries have been reported.

    Product
    V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended for intra hospital use under the direct supervision of a licensed healthcare practitioner. The indications for Use for the V Series include the monitoring of the following human…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2294-2012·2012-09-05

    Unimed Recalls Medline Electrosurgical Electrodes Due to Sterility Concerns

    Unimed Surgical Products is recalling Medline electrosurgical electrodes due to sterility concerns. The affected lot is 052709-01.

    Product
    Product is labeled in part: "***MEDLINE***Extended 5mm PTFE Coated Ball 5.0 (12.70cm) Length***Reorder: ES0009***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V482000·2012-09-03

    Morgan Olson Recalls 2009-2011 Walk-In Vans for Safety Standard Failures

    Morgan Olson is recalling 24 model year 2009-2011 Walk-In Vans because they fail to meet various Federal Motor Vehicle Safety Standards, potentially increasing crash risk.

    Product
    MORGAN OLSON — MORGAN OLSON WALK IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V433000·2012-08-31

    Quality Van Sales Recalls Ford E-Series Wheelchair Lifts

    Quality Van Sales is recalling 2006-2010 Ford E-Series vehicles with Braun wheelchair lifts due to bent roll stop latches that could cause occupant falls.

    Product
    QUALITY VAN SALES — QUALITY VAN SALES FORD E-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide