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.

42626–42650 of 50511

  • HighFDA (Food)·F-0098-2014·2013-11-06

    Price Chopper Apple Pie Recalled for Undeclared Eggs

    Price Chopper Supermarkets is recalling 10-inch apple pies because they contain undeclared eggs. The recall affects pies sold in New York, Connecticut, and Vermont.

    Product
    10 inch Apple Pie (baked and unbaked), NET WT 42 oz.(2 lb 10 oz), UPC 41735-22064 (unbaked) and 41735-23712 (baked), Price Chopper label.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0088-2014·2013-11-06

    Intuitive Surgical Recalls da Vinci Si Surgical Systems Due to Mounting Risk

    Intuitive Surgical is recalling 1,090 da Vinci Si Surgical Systems because improper restraints during transport could cause the monitor to become loose from its mount.

    Product
    da Vinci Si Surgical System IS3000 with the da Vinci Surgeon Console which contains a high Resolution Stereoscopic Viewer. Intended to assist in the accurate control of Intuitive Surgical Endoscopic instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0092-2014·2013-11-06

    Stryker TPS Micro Driver Recalled for Silicone Potting Defect

    Stryker is recalling 67 TPS Micro Drivers because silicone potting failed to cure properly, which could cause material leakage or electrical malfunction.

    Product
    REF 5100-088, TPS Micro Driver, For Use with Stryker Total Performance System Caution Federal Law (USA) restricts the device to use by or on the order of a physician Driver, Wire and Bone Drill; The Stryker Total Performance System (TPS) is intended for use in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0122-2014·2013-11-06

    Toshiba Diagnostic Ultrasound Systems Recalled for Transducer Overheating

    Toshiba is recalling 430 diagnostic ultrasound systems because the transducer head may overheat under specific operating conditions.

    Product
    Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic imaging
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0104-2014·2013-11-06

    Siemens Blood Gas Analyzers Recalled for Patient Identification Error Risk

    Siemens is recalling RAPIDPoint and RAPIDLab blood gas analyzers because users may enter wrong patient IDs, leading to sample misidentification.

    Product
    Siemens RAPIDPoint¿ 500 system blood gas analyzer Product Usage: RAPIDPoint 500 System: The RAPIDPoint 500 system is designed for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total hemoglobin, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0109-2014·2013-11-06

    Baxter Recalls Vented Spike Adapters Due to Potential Pouch Tears

    Baxter Healthcare is recalling 49,344 units of Vented Spike Adapters because potential tears in the pouch could compromise sterility.

    Product
    Vented Spike Adapter Product Code 2C0471, Sterile, nopyrogenic. Manufactured by an affiliate of Baxter Healthcare Corporation, Clintec Nutrition Division, Deerfield IL 60015 USA. An IV transfer device, used to transfer fluids in pharmacy compounding system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0067-2014·2013-11-06

    Philips Ingenuity TF PET/CT Software Recall for Potential Radiopharmaceutical Re-injection Risk

    Philips is recalling 13 Ingenuity TF PET/CT systems due to software issues that could require patients to be re-injected with PET radiopharmaceuticals during rescans.

    Product
    Ingenuity TF PET/CT Diagnostic imaging system for fixed or mobile installations that combines Positron Emission Tomography (PET) and X-Ray Computed Tomography (CT) systems. The CT subsystem produces cross sectional images of the body by computer reconstruction of x-ray…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V553000·2013-11-05

    Elite Cargo Trailer Recall for Door Lock Jamming Hazard

    Elite is recalling 2006-2013 cargo trailers with Fastec door locks that may jam, potentially trapping occupants inside.

    Product
    ELITE — ELITE CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13E062000·2013-11-05

    SK Innovation Recalls Econix DPF-A Diesel Particulate Filters Due to Fire Risk

    SK Innovation is recalling Econix DPF-A diesel particulate filters manufactured in August 2009 because missing maintenance instructions may cause the filter to melt, potentially leading to a fire.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V542000·2013-11-01

    Mercedes-Benz Recalls 2013 SL Models Due to Passenger Air Bag Defect

    Mercedes-Benz is recalling 130 model year 2013 SL63, SL550, and SL65 vehicles because the occupant classification system may fail to detect very light passengers, potentially disabling the side air bag.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SL65, SL63, SL550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14012·2013-10-31

    Calphalon Recalls Blenders Due to Blade Breakage Injury Hazard

    Calphalon is recalling approximately 22,000 XL 9 speed blenders in the U.S. and 400 in Canada because a piece of the mixing blade can break off, posing an injury hazard.

    Product
    Blenders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14010·2013-10-31

    Snoopy Sno-Cone Machines Recalled Due to Risk of Mouth Injury

    LaRose Industries is recalling Snoopy Sno-Cone Machines because a brass rivet can fall into the ice shavings, posing a risk of injury to the mouth or teeth.

    Product
    Snoopy Sno-Cone Machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0008-2014·2013-10-30

    Vinco's Fem-Vite Recalled Due to Potential Salmonella Contamination

    Vinco Inc. is recalling specific lots of Fem-Vite Women's Anti-Oxidant Formula because the soy ingredient may be contaminated with Salmonella.

    Product
    Vinco's Fem-Vite Women's Anti-Oxidant Formula, Dietary Supplement, 60 Tablets, distributed by Vinco, Inc., Evans City, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·13V541000·2013-10-30

    McLaren Recalls MP4-12C Vehicles for Wiper Motor Defect

    McLaren is recalling 2012-2014 MP4-12C vehicles in six states because wiper motors may stop working in hot, humid weather, increasing crash risk.

    Product
    MCLAREN — MCLAREN MP4-12C SPIDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V536000·2013-10-30

    Thomas Built Minotour School Bus Seat Barrier Recall

    Daimler Trucks North America is recalling 2013 Thomas Built Minotour school buses due to incorrect seat barrier installation that may increase injury risk in a crash.

    Product
    THOMAS BUILT — THOMAS BUILT MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0048-2014·2013-10-30

    Abbott Medical Optics Recalls STAR Excimer Laser Systems Due to Component Failure

    Abbott Medical Optics is recalling STAR Excimer Laser Systems due to a thyristor component failure that affects the lamp and illumination system.

    Product
    STAR Excimer Laser System with Variable Spot Scanning, Model: STAR S4, Catalog Number: 0030-4077, Product is manufactured and distributed by AMO Manufacturing USA, LLC, Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V537000·2013-10-30

    Thomas Built Buses Recall 2012-2014 Models for Missing Seat U-Bolts

    Daimler Trucks North America is recalling 328 Thomas Built Saf-T-Liner school buses because a U-bolt may be missing, which could cause seats to detach in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0058-2014·2013-10-30

    Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench

    Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because some contain a hex wrench that may not loosen the set screw on the drill bit.

    Product
    Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Probe Kit REF IM3.SR Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0050-2014·2013-10-30

    Convergent Dental Recalls Five Solea 1.0 Laser Surgical Instruments

    Convergent Dental is recalling five Solea 1.0 laser surgical instruments due to a defect that could cause unintended laser emission during activation.

    Product
    Solea 1.0 Laser Surgical instrument for use in general and plastic surgery and dermatology.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0049-2014·2013-10-30

    Abbott STAR Excimer Laser Systems Recalled for Thyristor Component Failure

    Abbott Medical Optics is recalling STAR Excimer Laser Systems due to a thyristor failure on the AC Power Distribution PCB that affects the lamp and illumination system.

    Product
    STAR Excimer Laser System, Model STAR S4 IR, Catalog Number: 0030-4864, Product is manufactured and distributed by AMO Manufacturing USA, LLC Milpitas, CA The STAR Excimer Laser Systems are indicated for laser assisted in situ keratomileusis (LASIK), photorefractive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0055-2014·2013-10-30

    Integra Licox Brain Tissue Oxygen Monitoring Kits Recalled for Defective Hex Wrench

    Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring kits because a hex wrench may fail to loosen the set screw on the drill bit.

    Product
    Integra Licox Brain Tissue Oxygen Monitoring; 1 x Dual Lumen Introducer Kit REF IP2; Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro, NJ…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V539000·2013-10-30

    Thomas Built Buses Recalls 2014 Saf-T-Liner C2 School Buses for Seat Rivets

    Daimler Trucks North America is recalling 73 model year 2014 Saf-T-Liner C2 school buses because improperly seated seat track rivets may prevent seat belts from working correctly in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14009·2013-10-30

    HeathCo Recalls Motion-Activated Outdoor Lights Due to Electrical Shock Hazard

    HeathCo is recalling about 223,000 motion-activated outdoor lights in the U.S. and Canada because the internal wiring can energize the fixture surface, posing an electrical shock hazard.

    Product
    Motion-Activated Outdoor Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0006-2014·2013-10-30

    Vinco's OsteoSheath Calcium Supplement Recalled for Potential Salmonella Contamination

    Vinco Inc. is recalling certain lots of OsteoSheath Enhanced Bone Support calcium supplements because the soy ingredient used in manufacturing was potentially contaminated with Salmonella.

    Product
    Vinco's OsteoSheath Enhanced Bone Support, Calcium Supplement, 90 Tablets, distributed by Vinco, Inc., Evans City, PA;
    Category
    Food
    Distribution
    Distributed nationwide