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.

42401–42425 of 50511

  • HighFDA (Devices)·Z-0381-2014·2013-12-04

    Biomet Recalls Oversized Security Blades for Carpal Tunnel Surgery

    Biomet, Inc. is recalling 1,130 Security Blades for carpal tunnel surgery because they were manufactured oversized and may be difficult to advance through the mating clip.

    Product
    REF 200068 Security (TM) Enclosed Carpal Tunnel System Blade ( Single) ABS /Stainless Steel Sterile Device, Single Use Only. Designed to release the transverse carpal ligament.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0396-2014·2013-12-04

    Synthes Titanium Spinal Locking Caps Recalled for Post-Operative Loosening

    Synthes USA is recalling 745 Titanium Minimally Invasive Reduction Screw System Locking Caps due to a risk of post-operative loosening if the construct is mis-aligned during final tightening.

    Product
    Synthes Titanium Minimally Invasive Reduction Screw System Locking Cap, Part Number 04.631.502 Non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0408-2014·2013-12-04

    Synthes Slipped Capital Femoral Epiphysis System Recalled for Drill Bit Breakage

    Synthes USA is recalling 166 units of the Slipped Capital Femoral Epiphysis System because guide wires may stick and drill bits may break during surgery.

    Product
    Slipped Capital Femoral Epiphysis System Product Usage: Intended for fracture fixation of large bones and large bone fragments and for slipped capital femoral epiphysis, pediatric femoral neck fractures, intercondylar femur fractures and sacroiliac joint disruptions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0389-2014·2013-12-04

    Las Trojes Mixed Seed Brittle Recalled for Undeclared Soy Lecithin

    Las Trojes is recalling Mixed Seed Brittle because it may contain undeclared soy lecithin. The product was distributed in California.

    Product
    Mixed Seed Brittle ("Pepitoria Mixed"), in cellophane packages, Net Wt. 2oz (57g), UPC 6 61444 00017 1.
    Category
    Food
    Distribution
    1 state
  • HighCPSC·14038·2013-12-04

    SRAM Recalls Bicycle Derailleurs Due to Fall Hazard

    SRAM is recalling specific RED WiFLi rear derailleurs because a pivot pin can loosen, causing the derailleur to jam and posing a fall hazard.

    Product
    Bicycle chain derailleurs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0422-2014·2013-12-04

    DePuy Recalls HP M.B.T. Keel Punch Knee Instruments Due to Fracture Risk

    DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.

    Product
    SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 2-3 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0357-2014·2013-12-04

    Plum Organics Yogurt Mish Mash Recalled for Contamination

    Plum Inc is recalling Plum Organics Tots Purple Roots and Fruits Yogurt Mish Mash due to a manufacturing defect that led to post-process contamination.

    Product
    Plum Organics Tots Purple Roots and Fruits Yogurt Mish Mash; 3.17 oz. Pouch; Also 12.69 oz. box. Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0392-2014·2013-12-04

    Las Trojes Pumpkin Seed Brittle Recalled for Undeclared Soy Lecithin

    Las Trojes is recalling specific lots of Pumpkin Seed Brittle because the product may contain undeclared soy lecithin, a common allergen.

    Product
    Pumpkin Seed Brittle ("Pepitoria"), in cellophane packages, Net Wt. 2 oz (57g), UPC 6 61444 0000 5 8.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0380-2014·2013-12-04

    Plum Inc Recalls Kale, Apple & Greekstyle Yogurt Pouches

    Plum Inc is recalling Kale, Apple & Greekstyle Yogurt pouches due to a manufacturing defect that led to post-process contamination.

    Product
    Kale, Apple & Greekstyle Yogurt Flexible pouch with Resealable spout. Packaged for individual sale in 6 count cartons and in 4 count packages. Best By dates ranging from 08/05/14 to 12/08/14 and the letters AT. DISTRIBUTED BY: NEST COLLECTIVE, INC. EMERYVILLE, CA 94608…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·14036·2013-12-03

    L&F International Trade Recalls Renovated Mattresses for Fire Hazard

    L&F International Trade is recalling about 1,000 renovated mattresses and mattress sets because they fail to meet federal flammability standards, posing a fire hazard.

    Product
    Mattresses and mattresses with foundations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V606000·2013-11-29

    Thomas Built Buses Recall School Buses for Seat Belt Defect

    Daimler Trucks North America is recalling 2013-2015 Thomas Built school buses because seat belt buckles may fail to release, hindering emergency egress.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS BUILT SAF-T-LINER HDX, MINOTOUR, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V618000·2013-11-29

    Volvo Recalls 2014 Trucks Due to Seat Belt Buckle Defect

    Volvo is recalling 5,486 model year 2014 trucks because seat belt buckles may fail to release, hindering emergency egress.

    Product
    VOLVO — VOLVO VAH, VNM, VHD, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V601000·2013-11-29

    E-One Recalls 2013 Fire Fighting Vehicles for Seat Belt Defect

    E-One is recalling 2013 Quest, Cyclone II, and Typhoon fire fighting vehicles because seat belt buckles may fail to release, hindering emergency egress.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON, QUEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V619000·2013-11-29

    Mack Trucks Recalls 2014 CXU and MRU Models for Seat Belt Defect

    Mack Trucks is recalling 2014 CXU and MRU trucks because seat belt buckles may fail to release, potentially hindering emergency egress.

    Product
    MACK — MACK MRU, PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V604000·2013-11-29

    Daimler Trucks Recalls 2014 Freightliner and Western Star Models for Seat Belt Defect

    Daimler Trucks North America is recalling 26,310 model year 2014 Freightliner and Western Star trucks because seat belt buckles may fail to release properly, hindering emergency egress.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 6900, CORONADO, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0343-2014·2013-11-27

    Siemens ADVIA 1200 Software Recalled for Ration Parameter Flagging Errors

    Siemens Healthcare Diagnostics is recalling ADVIA 1200 System Software versions 2.00 and 2.01 due to incorrect ration parameter flagging behavior.

    Product
    ADVIA 1200 System Software: 1) V2.00, 2) V2.01. Performs assays for general and specialty chemistries, methods for specific protein measurement, drugs-of-abuse testing and therapeutic drug monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0345-2014·2013-11-27

    Siemens ADVIA Chemistry System Software Recalled for Parameter Flagging Errors

    Siemens Healthcare Diagnostics is recalling ADVIA 1800 System Software V2.01 due to ration parameters flagging behavior issues.

    Product
    ADVIA 1800 System Software V2.01. Performs assays for general and specialty chemistries, methods for specific protein measurement, drugs-of-abuse testing and therapeutic drug monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0191-2014·2013-11-27

    Guzzler Concord Grape Beverage Recalled for Potential Cap Fragment Ingestion

    American Beverage Corp is recalling Guzzler Concord Grape beverages because a part of the nozzle cap may dislodge and be ingested.

    Product
    Guzzler Concord Grape 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0196-2014·2013-11-27

    Guzzler Orchard Chill bottles recalled due to potential cap dislodgement hazard

    American Beverage Corp is recalling Guzzler Orchard Chill bottles because the nozzle cap may dislodge if chewed, posing a choking or ingestion risk.

    Product
    Guzzler Orchard Chill, 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0204-2014·2013-11-27

    American Beverage Corp. Recalls Big Hug Fruit Barrel Citrus Bottles

    American Beverage Corp. is recalling Big Hug Fruit Barrel Citrus bottles due to a potential choking hazard from dislodged nozzle cap parts.

    Product
    Big Hug Fruit Barrel Citrus in a 16 oz plastic bottle with a sports cap, American Beverage Corp., Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0209-2014·2013-11-27

    American Beverage Corp. Recalls Big Burst Grape Drink Due to Cap Hazard

    American Beverage Corp. is recalling Big Burst Grape Drink because a part of the nozzle cap could become dislodged and ingested, posing a health hazard.

    Product
    Big Burst Grape Drink in a 16 oz PET plastic bottle with a sports cap, American Beverage Corp., Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0225-2014·2013-11-27

    Sunny Pine Farm Recalls Organic Honey Lavender Chevre for Pasteurization Concerns

    Sunny Pine Farm is voluntarily recalling Organic Honey Lavender Chevre due to possible improper pasteurization. The product was sold in Washington state.

    Product
    Organic Honey Lavender Chevre is sold in plastic 6 oz tubs under Sunny Pine Farm brand. The product is labeled in parts: "***Organic Goat Dairy***Honey Lavender Chevre***6 oz.***SUNNY PINE FARM***Handcrafted in Twisp, Washington 98856***Pasteurized Organic Goat Milk, Honey…
    Category
    Food
    Distribution
    1 state