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.

676–700 of 52881

  • HighFDA (Devices)·Z-2343-2026·2026-06-17

    MIC Safety 24 Fr push PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 24 Fr PUSH OTW, catalog number 7170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 132 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2314-2026·2026-06-17

    GE Allia IGS 3 Pulse systems pose shock risk to servicers

    Allia IGS 3 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Nine units affected.

    Product
    Allia IGS 3 Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2329-2026·2026-06-17

    CGuard Prime 10mm by 30mm carotid stents may fail deployment

    CGuard Prime Carotid Stent Systems, 135 cm with a 10 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.

    Product
    CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2350-2026·2026-06-17

    MIC Safety 14 Fr PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits with ENFit Connectors, 14 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2326-2026·2026-06-17

    CGuard Prime 8mm carotid stent systems may resist or fail deployment

    CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.

    Product
    Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2346-2026·2026-06-17

    MIC Safety 24 Fr pull PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2339-2026·2026-06-17

    CORFLO Safety PEG kit 50-6312 contains recalled lidocaine injection

    CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 43 kits affected.

    Product
    Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2313-2026·2026-06-17

    Plum Duo Precision IV pumps may not display soft limit alerts

    Plum Duo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.

    Product
    Plum Duo Precision IV Pump, 40002-0403
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V390000·2026-06-15

    Forest River Recalls 2023-2024 XLR Toy Haulers for Incorrect Weight Rating

    Forest River is recalling 2023-2024 XLR Toy Hauler trailers because the listed Gross Vehicle Weight Rating exceeds the chassis rating, creating a risk of overloading and crashes.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V385000·2026-06-12

    Winnebago Recalls 2026-2027 Revel Models Due to Incorrect Tire Label

    Winnebago is recalling 2026-2027 Revel and Revel Sport vehicles because the tire information label lists the wrong tire size, which could lead to incorrect replacements and increased crash risk.

    Product
    WINNEBAGO — WINNEBAGO REVEL, REVEL SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V389000·2026-06-12

    Land Rover recalls vehicles over corroding driver airbag clockspring connectors

    Jaguar Land Rover is recalling certain 2020-2026 Defender, 2021-2026 Discovery and 2022-2026 Range Rover vehicles because the driver's air bag clockspring connector may corrode.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, DISCOVERY, DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E034000·2026-06-12

    Marion Body Works Recalls Waltco Liftgates on Morgan Dry Vans

    Marion Body Works is recalling Waltco MDV series liftgates on Morgan aluminum dry vans because deck pins may break, causing the platform to fall.

    Product
    STRUCTURE:BODY:HATCHBACK/LIFTGATE:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V387000·2026-06-12

    Kawasaki Recalls 2025-2026 W230 Motorcycles Due to Turn Signal Defect

    Kawasaki is recalling 2025-2026 W230 motorcycles because defective turn signal bulbs may fail, increasing crash risk. Dealers will replace the lights free of charge.

    Product
    KAWASAKI — KAWASAKI W230
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E035000·2026-06-12

    Waymo Recalls 5th Generation Automated Driving Systems for Software Defect

    Waymo is recalling 5th Generation Automated Driving Systems because software may allow vehicles to enter closed freeway construction zones, increasing crash risk.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26536·2026-06-11

    Sloosh dive sticks violate federal ban and pose impalement hazard

    About 254,000 Sloosh dive sticks, sold in packages of Sloosh water toys model 40041, are being recalled because they exceed the compress limit under the federal dive sticks ban.

    Product
    Sloosh Dive Sticks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26555·2026-06-11

    Houoto pool drain covers lack required markings under federal law

    About 595 Houoto 642-2150V pool drain covers are being recalled because they lack required product markings under the Virginia Graeme Baker Pool and Spa Safety Act.

    Product
    Houoto 642-2150V Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide