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.

40101–40125 of 50506

  • HighNHTSA·14E078000·2014-11-17

    Carefree Latitude Awnings Recalled for Defective Screws on Motorhomes

    Carefree is recalling Latitude Awnings styles GX and G installed on motorhomes due to screws that may not meet specifications, posing a risk of the awning falling.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V734000·2014-11-17

    Fleetwood Bounder Classic Recalled for Loose Grab Bar Risk

    Allied Recreation Group is recalling 2014-2015 Fleetwood Bounder Classic RVs because a grab bar may pull loose, increasing injury risk.

    Product
    FLEETWOOD — FLEETWOOD BOUNDER CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E074000·2014-11-14

    FLY Racing Recalls Certain Model .357 Motorcycle Helmets

    FLY Racing is recalling specific Model .357 helmets because the retention strap ring may separate in high heat, increasing crash injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14E065000·2014-11-13

    Carefree Latitude Awning Recall Due to Cracking Mounting Brackets

    Carefree is recalling Latitude awnings because mounting brackets may crack, causing the awning to fall and potentially injure people underneath.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V729000·2014-11-13

    Starcraft Bus Recalls Transit Buses Due to Wheelchair Lift Defect

    Forest River is recalling 2006-2012 Starcraft transit buses because wheelchair lift platform side plates may crack, posing an injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS STARQUEST, ULTRASTAR, ALLSTAR, XLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V730000·2014-11-13

    Starcraft Bus Recalls School Buses with Cracking Wheelchair Lifts

    Forest River is recalling 2010-2012 Starcraft Bus Quest and Prodigy school buses because wheelchair lift platform side plates may crack, posing an injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS QUEST, PRODIGY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0159-2015·2014-11-12

    Terumo Cardiovascular Procedure Kits Recalled for Luer Connector Defect

    Terumo is recalling specific cardiovascular and perfusion procedure kits because a luer connector defect may compromise the seal and introduce air into the table line.

    Product
    Terumo Custom Cardiovascular and Perfusion Procedure Kits Catalog Codes: Kits with a 5-digit code beginning with the digit 6: Catalog Number: 6XXXX ; Catalog Codes: Kits with a 5-digit code beginning with the digit 7: Catalog Number: 7XXXX Product usage: The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0169-2015·2014-11-12

    Cynosure Elite XPL Handpiece Recalled for Electrical Shock Risk

    Cynosure, Inc. is recalling 322 Elite XPL handpieces for the Elite MPX Laser System due to a potential risk of electrical shock when the device is adjusted or removed while powered on.

    Product
    Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0178-2015·2014-11-12

    Dokitz NovoSci Recalls Cardiopulmonary Bypass Connectors Due to Detachment Risk

    Dokitz NovoSci is recalling 240 units of cardiopulmonary bypass connectors because the single leg of the PAY connector has been observed to become detached.

    Product
    Cardiopulmonary bypass connector; P/N: 321334-000 DESC: CONNECTOR, 3/8 X 3/8 X 1/2 CLEAR PAY LOT: 295424 STERILE Expiration May 2019 Manufacturing Date May 2014
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0157-2015·2014-11-12

    Terumo Cardioplegia Delivery Set Line Recalled for Luer Connector Defect

    Terumo is recalling 165 units of a cardioplegia delivery set line because a luer connector defect can compromise the seal and introduce air into the line.

    Product
    Terumo Custom Integrated Cardioplegia Delivery Set-LINE FOR 15501/16015/5852 Item Number: 16110 Product Usage: This is a replacement line to multiple Cardioplegia Delivery Sets - and includes the female luer connector that is the subject of this correction/removal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0158-2015·2014-11-12

    Terumo Cardioplegia Delivery Set Recalled for Luer Connector Seal Defect

    Terumo is recalling 777 Cardioplegia Delivery Sets because a defect in the luer connector can compromise the seal and introduce air into the tubing line.

    Product
    Terumo Cardioplegia Delivery Set- Item Number: 16130 Product Usage: The Cardioplegia Delivery Sets are indicated for delivery of cardioplegic solutions to the heart during cardiopulmonary bypass surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0457-2015·2014-11-12

    Buddy's Kitchen Recalls Fiesta Breakfast Scramble Due to Listeria

    Buddy's Kitchen, Inc. is recalling Fiesta Breakfast Scramble because an ingredient tested positive for Listeria monocytogenes.

    Product
    Fiesta Breakfast Scramble, Product # 73EN510. Net Weight 11.4 lbs. 24 - 7.60 oz. portions. Keep Frozen. For Institutional Use Only. Production Facility Buddy's Kitchen, Inc., Burnsville, MN 55337
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0160-2015·2014-11-12

    Terumo Custom Cardioplegia Delivery Set Recalled for Luer Connector Defect

    Terumo is recalling Custom Cardioplegia Delivery Sets because a defect in the luer connector can compromise the seal and introduce air into the tubing line.

    Product
    Terumo Custom Cardioplegia Delivery Set- Catalog Number:165720 and Catalog Number: 6375 Product Usage: Cardioplegia Delivery System that is designed to delivery blood/solution to the patient undergoing cardiopulmonary bypass surgery. The set is designed to deliver…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15022·2014-11-12

    Aqua Lung Recalls Buoyancy Compensators Due to Drowning Hazard

    Aqua Lung is recalling buoyancy compensators with SureLock II handles that may detach, posing a drowning risk. Consumers should stop using them and return them for free replacement.

    Product
    Aqua Lung buoyancy compensators with SureLock II weight pocket handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0161-2015·2014-11-12

    Terumo Custom Cardioplegia Delivery Sets Recalled for Luer Connector Seal Defect

    Terumo is recalling 24 units of Custom Cardioplegia Delivery Sets because a luer connector defect may compromise the seal and introduce air into the line.

    Product
    Terumo Custom Cardioplegia Delivery Sets Catalog Code: 204880 Product Usage: This is a replacement line to multiple Cardioplegia Delivery Sets-and includes the female luer connector" that is the subject of this correction/removal activity
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0165-2015·2014-11-12

    Zimmer Surgical Recalls Universal Modular Electric Handpieces Due to Malfunction

    Zimmer Surgical Inc is recalling 828 Universal Modular Electric/Battery Handpieces because a malfunction allows them to start unexpectedly when connected to a power source.

    Product
    UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric handpiece is packaged within a foam bag inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A product label is applied to the lid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0458-2015·2014-11-12

    United Natural Trading Recalls Asian 7 Rice Cracker Mix for Peanut Fragment

    United Natural Trading is recalling Asian 7 Rice Cracker Mix because a peanut fragment was found in the product. The recall affects 76 cases distributed in six states.

    Product
    The Market Basket Asian 7 Rice Cracker Mix Net Wt. 12 oz. (340 g) Distributed by Demondas Supermarkets, Inc. Tewksbury, MA 01876 UPC # 04970540898
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0459-2015·2014-11-12

    United Natural Trading Recalls Asian 7 Rice Cracker Mix Due to Peanut Fragment

    United Natural Trading is recalling Asian 7 Rice Cracker Mix because a peanut fragment was found in a carton. The product was distributed to specific facilities in Florida and Wisconsin.

    Product
    Asian 7 Rice Cracker Mix in Bulk 22 lb. cases; Wood Stock Farms Lot # YOUI03 sold to Publix Bakery Plant in Lakeland, FL, and to The Nutman Company - USA Inc., in Hubertus, WI.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0172-2015·2014-11-12

    Stryker SmartLife Aseptic Housings Recalled for Welding Defect

    Stryker is recalling SmartLife Large Aseptic Housings because the top section may separate from the bottom due to insufficient welding.

    Product
    Stryker SmartLife Large Aseptic Housing REF 7126-120-000 Rx Only The SmartLife" Aseptic Housings are designed to be used in conjunction with the SmartLife Non-Sterile Batteries to provide power for System 7 Handpieces, Cordless Driver 4 Handpiece, and Sabo2 Sagittal Saw…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0163-2015·2014-11-12

    C.R. Bard Recalls 86 Non-Sterile Bard Dimension Stone Baskets

    C.R. Bard is recalling 86 non-sterile Bard Dimension Stone Baskets due to a Class II recall classification.

    Product
    Bard Dimension Stone Basket Product Usage: The Bard Dimension Stone basket is a teardrop-shaped basket with the ability to capture stones by, opening and closing the basket and articulating or moving the basket from side to side. The device consists of 3 main parts; handle…
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-0173-2015·2014-11-12

    Stryker SmartLife Aseptic Housings Recalled for Welding Defect

    Stryker is recalling SmartLife Small Aseptic Housings because the top section may separate from the bottom due to insufficient welding.

    Product
    Stryker SmartLife Small Aseptic Housing REF 7222-120-000 Rx Only The SmartLife" Aseptic Housings are designed to be used in conjunction with the SmartLife Non-Sterile Batteries to provide power for System 7 Handpieces, Cordless Driver 4 Handpiece, and Sabo2 Sagittal Saw…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15021·2014-11-10

    McDonald's Recalls Hello Kitty Whistles Due to Choking Hazard

    McDonald's is recalling Hello Kitty Birthday Lollipop Whistles because internal components can detach, posing choking and aspiration risks to young children.

    Product
    Hello Kitty® Birthday Lollipop Whistles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V718000·2014-11-10

    Sutphen Aerial Devices Recalled for Potential Ladder Cable Failure

    Sutphen is recalling 2000-2014 aerial devices because a cable failure could cause the ladder to collapse, increasing injury risk.

    Product
    SUTPHEN — SUTPHEN SPI 112, SPH 100, SP 110, SAI 110
    Category
    Vehicle
    Distribution
    Distributed nationwide