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.

22676–22700 of 50430

  • HighFDA (Devices)·Z-2629-2020·2020-07-22

    Skeletal Kinetics Recalls SKAFFOLD FLOW Bone Void Filler Kits

    Skeletal Kinetics is recalling SKAFFOLD FLOW bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life, potentially increasing surgical time or causing bone formation issues.

    Product
    SKAFFOLD FLOW, 10CC. Product Number: SKMX-FL10, UDI: 813845020900 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1054-2020·2020-07-22

    Fresh Express 3 Color Deli Cole Slaw Recalled for Cyclospora Risk

    Fresh Express is recalling 14 oz 3 Color Deli Cole Slaw due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.

    Product
    Fresh Express America's Fresh 3 Color Deli Cole Slaw" 14 oz, UPC 071279123004, (Canada UPC) 0 71279 12302 8 , Green cabbage, carrots & red cabbage
    Category
    Food
    Distribution
    32 states
  • HighFDA (Devices)·Z-2634-2020·2020-07-22

    Skeletal Kinetics Recalls Craniosculpt Bone Void Filler Kits

    Skeletal Kinetics is recalling Craniosculpt bone void filler kits because they may not maintain setting characteristics for the labeled shelf life.

    Product
    CRANIOSCULPT, CMF IMPACT, 5CC, Product Number: C-CMF5CC, UDI: 813845020948 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1102-2020·2020-07-22

    Fresh Express Southwest Salad Recalled for Cyclospora Risk

    Fresh Express is recalling Hy-Vee Chopped Kit Southwest Salad due to a possible health risk from Cyclospora. Consumers should not eat the product.

    Product
    Hy-Vee Chopped Kit Southwest Salad 13.4 oz., UPC 075450246698, Red & green cabbage, green leaf lettuce, carrots & green onions
    Category
    Food
    Distribution
    32 states
  • HighFDA (Food)·F-1085-2020·2020-07-22

    Fresh Express Recalls Giant Eagle Chopped BBQ Ranch Salad Kits

    Fresh Express is recalling Giant Eagle Chopped BBQ Ranch Salad Kits due to a possible health risk from Cyclospora contamination.

    Product
    Giant Eagle Chopped BBQ Ranch Salad Kit 11.3 oz., UPC 030034923303, Cabbage and lettuce, carrots, and green onion
    Category
    Food
    Distribution
    32 states
  • HighFDA (Food)·F-1123-2020·2020-07-22

    Fresh Express Marketside Chopped Salad Kit Recalled for Cyclospora Risk

    Fresh Express is recalling Marketside Chopped Salad Kits due to a possible health risk from Cyclospora. Consumers should not consume the affected products.

    Product
    Marketside Chopped Salad Kit Sunflower Bacon Crunch 13.8 oz., UPC 681131148344, Green & red cabbage, kale, romaine lettuce, green onions & carrots
    Category
    Food
    Distribution
    32 states
  • HighNHTSA·20V421000·2020-07-21

    Newmar Recalls Motorhomes with Damaged Rear Power Distribution Modules

    Newmar is recalling specific 2016-2020 motorhomes because a damaged rear Power Distribution Module may cause exterior lights to stop working, increasing crash risk.

    Product
    NEWMAR — NEWMAR LONDON AIRE, ESSEX, NEW AIRE, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V419000·2020-07-20

    2021 Thor Motor Coach motorhomes recalled for battery cable fire risk

    Thor Motor Coach is recalling 2021 motorhomes because an improperly secured battery cable may contact the exhaust manifold and pose a fire risk. Owners should contact Thor Motor Coach for a free inspection and repair.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH DAYBREAK, FOUR WINDS, QUANTUM, CHATEAU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V420000·2020-07-20

    Altec Recalls 1995-1998 Aerial Devices Due to Hydraulic Cylinder Defect

    Altec Industries is recalling 1995-1998 A0442 aerial devices because a hydraulic cylinder end gland may fail, causing uncontrolled boom movement and increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V416000·2020-07-17

    Mercedes-Benz Recalls 2019 A 220 Vehicles for Electrical Water Ingress Risk

    Mercedes-Benz is recalling 2019 A 220 vehicles because a poorly installed air conditioning drain hose may allow water to enter electrical components, potentially causing system malfunctions.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ A 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V413000·2020-07-17

    Ford recalls 2021 F-650 and F-750 trucks for missing heat shields

    Ford is recalling certain 2021 F-650 and F-750 trucks because heat-protection components were not installed during assembly. Without these shields, the cabin floor and seat attachments may become too hot and cause burns.

    Product
    FORD — FORD F-650 SD, F-750 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E049000·2020-07-17

    Allison Transmission Drive Units Recalled for Pressure Switch Failure

    Allison Transmission is recalling specific drive units because pressure switches may fail, potentially causing a loss of drive and increasing crash risk.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20150·2020-07-16

    Rocky Mountain Recalls Alloy Instinct and Pipeline Bicycles Due to Frame Cracking

    Rocky Mountain is recalling about 1,530 non-electric alloy frame Instinct and Pipeline bicycles because the front frame triangle can crack, posing fall and injury hazards.

    Product
    Rocky Mountain non-electric alloy frame Instinct, Instinct BC and Pipeline bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20764·2020-07-16

    Polaris Recalls 2015-2020 AXYS Snowmobiles Due to Fire Hazard

    Polaris is recalling approximately 41,200 AXYS snowmobiles because improperly secured fuel hoses may pose a fire hazard. No fires or injuries have been reported.

    Product
    Model Year 2015-2020 AXYS Trail Performance and Crossover snowmobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2528-2020·2020-07-15

    TeDan Phantom CS Quick Start Distraction Screw Recall for Seal Defect

    TeDan Surgical Innovations LLC is recalling 730 sterile Phantom CS Quick Start Distraction Screws due to a lack of pouch seal.

    Product
    PHANTOM CS QUICK START DISTRACTION SCREW, 12 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2497-2020·2020-07-15

    Ra Medical Systems Recalls DABRA Laser Due to Software Issue

    Ra Medical Systems is recalling 79 DABRA Laser units because a software issue could cause unintended laser light release, potentially injuring users or patients.

    Product
    DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and delivery system, collectively the DABRA Laser System". The system is designed to deliver the energy to the surgical site to ablate unwanted material. The…
    Category
    Medical Device
    Distribution
    22 states
  • HighCPSC·20148·2020-07-15

    Simplers Botanicals Wintergreen Essential Oil Recalled for Packaging Defect

    Nutraceutical is recalling Simplers Botanicals Wintergreen Essential Oil because the packaging is not child-resistant, posing a poisoning risk.

    Product
    Simplers Botanicals Organic Wintergreen (Gaultheria Fragrantissiam) Essential Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2519-2020·2020-07-15

    Kentec Medical Recalls ENFit Feeding Tubes Due to Cap Fracture Risk

    Kentec Medical is recalling 70 ENFit feeding tubes because the plastic tethered closure cap may fracture, potentially delaying care or causing unnecessary radiation exposure.

    Product
    Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number ENF-Y50P-80 (5 fr. 80 cm ENFit Enteral Feeding Tube with Y-Port).
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-2492-2020·2020-07-15

    Prodimed Combicath Paediatric Catheters Recalled for Sterility Assurance Issues

    Prodimed is recalling Combicath Paediatric catheters due to a lack of assurance of sterility. The recall covers 2,580 units distributed nationwide.

    Product
    Prodimed Combicath Paediatric catheters for blind protected distal bronchial sampling-" COMBICATH PE 35 cm Product Code: 58 223 19
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2529-2020·2020-07-15

    TeDan Phantom CS Distraction Screw Recalled for Sterility Seal Defect

    TeDan Surgical Innovations LLC is recalling 495 Phantom CS Quick Start Distraction Screws because the pouch seal is lacking, compromising the sterile labeling.

    Product
    PHANTOM CS QUICK START DISTRACTION SCREW, 14 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior approach to the cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2520-2020·2020-07-15

    Kentec Medical Recalls ENFit Enteral Feeding Tubes Due to Cap Fracture Risk

    Kentec Medical is recalling 170 ENFit enteral feeding tubes because the plastic tethered closure cap may fracture or break, potentially delaying patient care.

    Product
    Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number ENF-Y60P-80 (6 fr. 80 cm ENFit Enteral Feeding Tube with Y-Port).
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-2487-2020·2020-07-15

    Prodimed Combicath Catheters Recalled for Sterility Assurance Concerns

    Prodimed Plastimed Division is recalling 7,220 Combicath catheters for mini bronchoalveolar lavage due to a lack of assurance of sterility.

    Product
    Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 60 cm x 2.7 mm Product Code: 58216 27US
    Category
    Medical Device
    Distribution
    Distributed nationwide