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.

15351–15375 of 53092

  • HighFDA (Devices)·Z-0215-2023·2022-11-23

    GENESIS Full-Length Sterilization Containers recalled for failed aerosol testing

    CareFusion 2200 Inc recalls GENESIS sterilization containers (model CD3-7ST, all lots) that have not consistently met aerosol challenge testing requirements required for proper sterilization efficacy.

    Product
    CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 7" (17.8CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD3-7ST
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0213-2023·2022-11-23

    CareFusion Genesis Sterilization Containers Fail Validation Testing

    CareFusion GENESIS sterilization containers have failed aerosol challenge testing for STERRAD sterilization validation. The recall affects 451 units distributed in the US and 17 other countries.

    Product
    CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD3-5ST
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0241-2023·2022-11-23

    GI4000 Electrosurgical Unit recalled due to power regulator failure risk

    Steris recalls 5 GI4000 Electrosurgical Units with defective diode components that may cause power loss during endoscopic procedures.

    Product
    GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to perform cutting and/or coagulation and coagulation with or without delivery of argon gas, in flexible endoscopic applications. MODEL #(s): G1110001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0245-2023·2022-11-23

    Infection Control Lifting Strap Recalled for Patient Safety Risk Due to Breakage

    Tollos is recalling Infection Control (IC) Lifting Straps used with certain Cirrus and Pinnacle ceiling lifts because the straps can break during patient lifts, potentially causing patients or caregivers to be injured by falls.

    Product
    Infection Control (IC) Lifting Strap used with the following Cirrus and Pinnacle Ceiling Lifts: Cirrus 450, Cirrus 600, Cirrus 700, Cirrus 750, and Pinnacle 1000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0243-2023·2022-11-23

    EasyStand Bantam standing devices may fail to maintain upright position

    Altimate Medical is recalling EasyStand Bantam Small and Extra Small standers due to a component defect that may prevent the leg assembly bracket from maintaining the non-supine position. No injuries have been reported.

    Product
    EasyStand Bantam, with the following sizes. a. Small; b. Extra Small. Used for assisting individual in standing.
    Category
    Medical Device
    Distribution
    7 states
  • HighNHTSA·22V864000·2022-11-22

    ATC Recalls 2022 Toyhauler Trailers Due to Awning Seam Defect

    ATC is recalling 2022 Toyhauler-20-foot trailers because a welded seam on the electric retractable awning may separate, allowing the awning to drop and increase injury risk.

    Product
    ATC — ATC TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V860000·2022-11-21

    BMW Recalls 2023 Models for Telematics Location Transmission Defect

    BMW is recalling 2023 740i, 760i, and i7 vehicles because the telematics unit may fail to send location data to emergency responders, potentially delaying aid.

    Product
    BMW — BMW 740I, 760I, I7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V862000·2022-11-21

    Genuine Scooter Recalls 2022 Buddy Kick 125 for Fuel Pump Defect

    Genuine Scooters is recalling 2022 Buddy Kick 125 motorcycles because a fuel pump defect may cause loss of drive power, increasing crash risk.

    Product
    GENUINE SCOOTER — GENUINE SCOOTER BUDDY KICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V854000·2022-11-18

    2023 Toyota Tundra pickup truck load capacity label correction

    Certain 2023 Toyota Tundra trucks with spray-on bed liners have incorrect load capacity labels that may indicate less weight than actually installed. This could lead to vehicle overloading and increased crash risk. Owners will receive free replacement labels.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V859000·2022-11-18

    Ford Escape and Bronco Sport fuel injector leak fire risk

    Ford is recalling certain 2020-2023 Escape and 2021-2023 Bronco Sport vehicles with 1.5L engines due to fuel injector cracks that may leak fuel and increase fire risk. Ford will update engine control software and install a drain tube.

    Product
    FORD — FORD ESCAPE, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V857000·2022-11-18

    Shyft Group Recalls 2023 Utilimaster Walk-in Vans for Missing Seat Clip

    Shyft Group is recalling 2023 Utilimaster Walk-in vans because a missing safety clip on the passenger jump seat may allow it to fall, increasing injury risk.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V853000·2022-11-18

    Midwest Fire Recalls 2021-2022 All-Poly Series Fire Trucks

    Midwest Fire is recalling 2021-2022 All-Poly Series fire trucks because a software defect may prevent shifting between road and pump modes, potentially delaying emergency response.

    Product
    MIDWEST FIRE — MIDWEST FIRE ALL-POLY SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V849000·2022-11-17

    2021-2023 International MV Vehicles Recalled for High-Voltage Cable Mislabeling

    Navistar is recalling certain 2021-2023 International MV vehicles due to mislabeled high-voltage battery cables that could be mistaken for de-energized cables, risking electrical shock to technicians or first responders.

    Product
    INTERNATIONAL — INTERNATIONAL MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23049·2022-11-17

    Children's Rainbow Stacking Toys Recalled Due to Choking Hazard

    Professor Puzzle's rainbow stacking toys are recalled because the toy's information sticker can detach and pose a choking hazard to young children. No injuries have been reported.

    Product
    Rainbow Stacking Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23048·2022-11-17

    Infant Yellow Footed Fleece Pajamas Recalled for Puncture and Laceration Hazards

    The William Carter Company is recalling about 50,800 infant yellow footed fleece pajamas because small metal wire pieces found in the garment pose puncture and laceration hazards to young children. No injuries have been reported.

    Product
    Infant's Yellow Footed Fleece Pajamas with Animal Graphic
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0189-2023·2022-11-16

    Cardinal Health Insulated Gel Pack Recalled for Infant Safety

    Cardinal Health is recalling its insulated gel pack because it should not be used on infants or neonates. The product labeling will be updated with a caution statement.

    Product
    Cardinal Health INSULATED GEL PACK REUSABLE, SMALL, Cat. 80204A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0194-2023·2022-11-16

    Insulin Pump Cybersecurity Vulnerability Allows Unauthorized Remote Access

    MiniMed 600 series insulin pumps have a cybersecurity vulnerability that could allow unauthorized access, potentially resulting in delivery of too much or too little insulin. Users should disable the Remote Bolus feature.

    Product
    Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711, MMT-1712, MMT-1751, MMT-1752
    Category
    Medical Device
    Distribution
    54 states
  • HighFDA (Devices)·Z-0222-2023·2022-11-16

    X-Guide X-Mark Probe Tool Recall: Missing Weld Creates Aspiration Risk

    X-NAV Technologies is recalling the X-Guide X-Mark Probe Tool because a critical weld may be missing, potentially allowing the probe tip to detach and fall into a patient's mouth during use, creating a risk of aspiration or swallowing.

    Product
    X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog Number:P010673
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0143-2023·2022-11-16

    BabyBel Snacker Cheese Recall: Undeclared Milk and Almond Allergens

    Taylor Farms Retail is recalling BabyBel Snacker cheese products due to undeclared milk and almond allergens on the ingredient label. Consumers with allergies to these ingredients should not consume the product.

    Product
    BabyBel Snacker (FG0401 SW Snacker ACABB 5pk) Crunch Pak 5.75 oz In sealed plastic tray, 5 trays per case UPC: 732313001572 Keep refrigerated Crunch Pak Item Number - FG0401
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0178-2023·2022-11-16

    La Rosa Brand Pasteurized Crabmeat Recalled for Defective Seal

    RIVER CITY SEAFOOD INTERNATIONAL LLC is recalling 51 cases of La Rosa Brand BluCrab Pasteurized Crabmeat (lot #0531, best by 11/2023) due to defective seals that could allow contamination.

    Product
    La Rosa Brand BluCrab Pasteurized Crabmeat (Jumbo, Lump, Claw) Peso Neto: 454g Can label art is the same for all cans, there is a sticker for each category (Jumbo, Lump, Claw) that goes on the lid.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0183-2023·2022-11-16

    Zio AT Ambulatory ECG Monitoring System Documentation Labeling Update

    iRhythm Technologies is recalling clinical reference materials for the Zio AT cardiac monitoring system due to labeling deficiencies that may delay notification of arrhythmias to healthcare providers. Transmission limits could prevent critical cardiac event reporting.

    Product
    Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio Ambulatory ECG monitoring system
    Category
    Medical Device
    Distribution
    48 states