The Recall Desk

Hazard

Ingestion recalls

102 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
102
Critical
4
Severe
10
Most recent
2026-09-03

Of the 102 ingestion recalls we have scored against our rubric, 4 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 10 (10%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all ingestion recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–25 of 102

  • SevereCPSC·26717·2026-08-27

    Conair Recalls Cuisinart Grill Brushes Due to Ingestion Hazard

    Conair is expanding a recall of over 3.6 million Cuisinart grill brushes because metal wire bristles can detach and be swallowed, posing a risk of serious internal injury.

    Product
    Metal Wire Bristle Grill Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26719·2026-08-27

    HABA Rainbow Rattle Toy Recalled Due to Choking and Ingestion Hazards

    HABA USA is recalling Rainbow Rattle Grasping and Teething Toys because a glued knot can untie, exposing small parts that pose choking and ingestion risks to young children.

    Product
    HABA Rainbow Rattle Grasping and Teething Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26650·2026-07-30

    Movie souvenir cups and popcorn helmets recalled for button battery ingestion hazard

    About 55,350 Fantastic Four drinking cups and Captain America popcorn helmets with LED lights have accessible button cell batteries and lack the warning labels required by Reese's Law.

    Product
    Fantastic Four Drinking Cups and Captain America Popcorn Helmet Containers with LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26164·2025-12-18

    Toy play purse sets recalled over accessible button and coin batteries

    About 3,090 Meaicezli Play Purse Sets are being recalled because the toy cell phone contains button cell batteries and the toy tablet a lithium coin battery that children can easily access.

    Product
    Meaicezli Play Purse Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26133·2025-12-04

    Treehouse building sets recalled over accessible button cell batteries

    About 40 Cubimana treehouse building toy sets are being recalled because button cell batteries in the LED light piece can be easily accessed by children.

    Product
    Cubimana Treehouse Building Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26085·2025-11-13

    Doll sets recalled over button cell batteries children can easily reach

    About 380 Bettina Doll Sets with Magic Light Unicorn are being recalled because the unicorn's battery compartment lets children easily access button cell batteries.

    Product
    Bettina Doll Set with Magic Light Unicorn
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26089·2025-11-13

    Coin battery packs recalled for missing child resistant packaging and warnings

    About 32,600 Great Lakes Select button cell and coin battery packs are being recalled because they lack the child-resistant packaging and warning labels required under Reese's Law.

    Product
    Great Lakes Select Button Cell and Coin Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25294·2025-05-22

    Primark DTR Plush Bag Stitch and Angel Recalled for Choking Hazard

    Primark is recalling DTR Plush Bag Stitch and DTR Plush Bag Angel products because the zipper pull can detach, posing a choking and ingestion risk to children.

    Product
    DTR Plush Bag Stitch and DTR Plush Bag Angel
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25142·2025-02-20

    Fjorden iPhone Camera Grips Recalled for Coin Battery Ingestion Hazard

    Fjorden iPhone Camera Grips can release their coin batteries if dropped, creating an ingestion hazard for children. Swallowed coin batteries can cause serious internal injuries, chemical burns, and death.

    Product
    Fjorden iPhone Camera Grips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24048·2023-12-07

    XpressGoods recalls magnetic balls for federal toy safety violations

    XpressGoods is recalling colorful neodymium magnetic balls that exceed federal safety limits for toy magnets. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.

    Product
    Colorful Metal Neodymium Magic Magnetic Balls - 8 color, 5mm
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24049·2023-12-07

    Primark Baby Rattles Recalled for Choking and Ingestion Risk

    Primark is recalling about 1,380 Wooden Music Shaker and DTR M&M Maracas baby rattles because the bottom portion can detach, creating a choking and ingestion hazard for children.

    Product
    Wooden Music Shaker and "DTR M&M Maracas" Baby Rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·23286·2023-09-14

    Chuckle & Roar Ultimate Water Beads Activity Kits Recalled for Ingestion and Choking Hazards

    Buffalo Games and Target are recalling Chuckle & Roar Ultimate Water Beads Activity Kits because ingested water beads expand and can cause choking and intestinal obstruction in children. One infant death and one serious injury requiring surgery have been reported.

    Product
    Chuckle & Roar Ultimate Water Beads Activity Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0223-2023·2022-11-16

    Neonatal Endotracheal Tube Grip with Detachable Metal Clips Recalled

    CooperSurgical is recalling NEO-fit Neonatal Endotracheal Tube Grips due to metal clips that can become loose or detach. Eleven complaints include three cases of clip ingestion, three removals from the mouth, and one throat laceration.

    Product
    NEO-fit Neonatal Endotracheal Tube Grip, Part Number 42-2540
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1956-2021·2021-07-21

    Philips Respironics Continuous Ventilators Recalled for Foam Degradation Risk

    Philips Respironics is recalling approximately 255,810 continuous ventilators because polyurethane foam may degrade into particles that could be inhaled or ingested, or release chemicals.

    Product
    Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent Continuous Ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20741·2020-05-07

    Sobeauty Recalls Mag Cube Magnetic Ball Sets Due to Ingestion Risk

    Sobeauty is recalling Mag Cube magnetic ball sets because the small, high-powered magnets pose a serious risk of intestinal injury or death if swallowed by children.

    Product
    Mag Cube magnetic ball sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0790-2020·2020-01-15

    Implant Direct IO Scan Adapter Recalled Due to Loose Component

    Implant Direct is recalling 274 IO Scan Adapters because a loose part could fall into a patient's mouth, posing a risk of aspiration or ingestion.

    Product
    ImplantDirect InterActive Precision IO Scan Adapter, Part #6534-09PT, Platform: 3.4mm, Non-Sterile, Rx. The firm name on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA.
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0791-2020·2020-01-15

    Implant Direct IO Scan Adapter Recall Due to Loose Component

    Implant Direct Sybron Manufacturing is recalling 232 IO Scan Adapters because a loose part could fall into a patient's mouth, causing aspiration or ingestion.

    Product
    ImplantDirect InterActive Precision IO Scan Adapter, Part #6530-09PT, Platform: 3.0mm, Non-Sterile, Rx. The firm name on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA.
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-0719-2020·2020-01-01

    3M Recalls Durapore Advanced Surgical Tape Due to Bond Failure Risk

    3M is recalling Durapore Advanced Surgical Tape because long-term exposure to high moisture may cause bond failure and fiber fraying, posing a risk of accidental ingestion or aspiration.

    Product
    3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-0, 1590-1, 1590-2, 1590-3, 1591-0, 1591-1, 1591-2, 1591-3, 1590S-1, 1590S-2, 1590B-118, 1590B-136
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0094-2019·2018-10-17

    Widex BABY Hearing Aids Recalled for Non-Tamper-Resistant Battery Drawers

    Widex A/S is recalling two BABY440 hearing aids because they were fitted with non-tamper-resistant battery drawers. The devices were distributed in Georgia and New York.

    Product
    Widex BABY hearing aid (referred to as BABY440), powered by zinc-air batteries size 10 Intended use: BABY440 is intended for, but not limited to, babies (0 to 3 years of age) to be used as air conduction amplification devices in everyday listening environments.
    Category
    Medical Device
    Distribution
    2 states