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.

36376–36400 of 50504

  • HighFDA (Devices)·Z-1128-2016·2016-03-23

    Zimmer Manufacturing Recalls Free-Lock Lag Screws Due to Sterility Concerns

    Zimmer Manufacturing B.V. is recalling 3,500 units of Free-Lock Lag Screws and related bone fixation products due to insufficient sealer calibration data affecting sterility.

    Product
    Product 30 consists of all product under product code: KTT and same usage: Item no: 118100527 FREE-LOCK LAG SCREW, 12.7 118100535 FREE-LOCK LAG SCREW, 12.7 118100540 FREE-LOCK LAG SCREW, 12.7 118100542 FREE-LOCK LAG SCREW, 12.7 118101022 FREE-LOCK LAG SCREW, 12.7…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1184-2016·2016-03-23

    Stryker Recalls Prime Series Stretchers Due to Hydraulic Jack Oil Error

    Stryker is recalling 36 Prime Series Stretchers because hydraulic jack assemblies were filled with incorrect oil, increasing the risk of leaks or jack drift.

    Product
    Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom) Powered stretcher
    Category
    Medical Device
    Distribution
    15 states
  • HighNHTSA·16V167000·2016-03-23

    Chrysler Recalls 2015-2016 Ram 1500 Trucks for Steering Assist Loss

    Chrysler is recalling 2015-2016 Ram 1500 trucks because contamination on the electric power steering circuit board may cause a short, resulting in the loss of power steering assist.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1169-2016·2016-03-23

    Zimmer Versis Press Fit Hip Components Recalled for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling 2,388 Versis Press Fit hip arthroplasty components due to insufficient sealer calibration data, raising concerns about the sterility of the devices.

    Product
    Product 71 consists of all product under product code: JDI and same usage: Item no: 783401000 VERSYS PRESS FIT LD/FX ST 783401100 VERSYS PRESS FIT LD/FX SZ 783401200 VERSYS PRESS FIT LD/FX SZ 783401300 VERSYS PRESS FIT LD/FX SZ 783401400 VERSYS PRESS FIT LD/FX SZ…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1152-2016·2016-03-23

    Zimmer NexGen Taper Plug Recalled for Insufficient Sealer Calibration Data

    Zimmer Manufacturing B.V. is recalling 1,767 NexGen Taper Plugs used in total knee arthroplasty due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.

    Product
    Product 54 consists of all product under product code: JWH and same usage: Item no: 596009900 NEXGEN TAPER PLUG for use in total knee arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1149-2016·2016-03-23

    Zimmer NexGen Option Stemmed Tibia Recalled for Sterility Concerns

    Zimmer Manufacturing B.V. is recalling NexGen Option Stemmed Tibia components due to insufficient sealer calibration data, raising concerns about the sterility of the devices.

    Product
    Product 51 consists of all product under product code: JWH and same usage: Item no: 598603701 NEXGEN OPTION STEMMED TIB 598603702 NEXGEN OPTION STEMMED TIB 598604701 NEXGEN OPTION STEMMED TIB 598604702 NEXGEN OPTION STEMMED TIB 598605701 NEXGEN OPTION STEMMED TIB…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1187-2016·2016-03-23

    Medtronic Recalls Covidien Emprint Percutaneous Antenna Due to Generator Shutdown Risk

    Medtronic is voluntarily recalling specific lots of the Covidien Emprint Percutaneous Antenna because the generator may shut down during high-temperature measurements.

    Product
    Short Percutaneous Antenna with Thermosphere" Technology Standard Percutaneous Antenna with Thermosphere" Technology; The product is packaged in a blister with a tyvek lid, contained in a display box. The numbers of units per carton is 1. Long Percutaneous Antenna with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1141-2016·2016-03-23

    Zimmer Manufacturing Recalls Sterile Intramedullary Nails Due to Sealer Calibration Issues

    Zimmer Manufacturing B.V. is recalling 1,102 sterile intramedullary nails distributed nationwide. The recall is due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.

    Product
    Product 43 consists of all product under product code: HSB and same usage: Item no: 224001016 M/DN R-F IM NAIL 10MM DIA 224001018 M/DN R-F IM NAIL 10MM DIA 224001020 M/DN R-F IM NAIL 10MM DIA 224001022 M/DN R-F IM NAIL 10MM DIA 224001024 M/DN R-F IM NAIL 10MM DIA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1113-2016·2016-03-23

    Zimmer Astel Femoral Head Recall Due to Sealer Calibration Data

    Zimmer Manufacturing B.V. is recalling sterile Astel femoral heads for hip arthroplasty due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.

    Product
    Product 15 consists of all product code JDI , and same usage: Item no: 805002802 ASTEL FEM HEAD +0X28MM DI 805002805 ASTEL FEM HEAD +10.5X28MM 805002803 ASTEL FEM HEAD +3.5X28MM 805002804 ASTEL FEM HEAD +7X28MM DI 805002801 ASTEL FEM HEAD -3.5X28MM Usage: For use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1162-2016·2016-03-23

    Zimmer Manufacturing Recalls Unipolar Endo Femoral Heads Due to Sealer Calibration Issues

    Zimmer Manufacturing B.V. is recalling specific unipolar endo femoral heads used in hip arthroplasty due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.

    Product
    Product 64 consists of all product under product code: JDI and same usage: Item no: 902605101 UNIPOLAR ENDO FEM HEAD 51MM For use in hemi hip arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V164000·2016-03-22

    Forest River Recalls 2016 Cherokee Grey Wolf Trailers for Placard Error

    Forest River is recalling 2016 Cherokee Grey Wolf recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which may lead to overloading and tire blowouts.

    Product
    CHEROKEE — CHEROKEE GREY WOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V165000·2016-03-22

    Weiler Trucks Recalled for Missing Reflectors on LED Marker Lights

    Weiler is recalling 368 trucks from 2002-2016 because LED marker lights lack required reflectors, reducing visibility and increasing crash risk.

    Product
    WEILER — WEILER WT4000, B3, F5, M100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16126·2016-03-21

    Panasonic Recalls Lithium-ion Laptop Battery Packs Due to Fire Hazard

    Panasonic is recalling specific lithium-ion battery packs for CF-S10 Series laptops because a manufacturing defect poses a fire risk. No injuries have been reported.

    Product
    Lithium-ion Computer Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16123·2016-03-18

    IKEA Recalls Gothem Floor and Table Lamps Due to Shock Hazard

    IKEA is recalling about 30,600 Gothem floor and table lamps because damaged cables can contact the metal body, posing a shock hazard. Consumers should stop using the lamps and return them for a full refund.

    Product
    Gothem floor and table lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E022000·2016-03-18

    ISS Recalls Evercraft Jack Stands Due to Potential Weld Defects

    International Specialty Services is recalling Evercraft jack stands sold by NAPA Auto Parts because improper welds may cause the stands to collapse, posing an injury risk.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V158000·2016-03-17

    Jayco Recalls 2016 White Hawk Travel Trailers Due to Axle Defect

    Jayco is recalling 10 model year 2016 White Hawk travel trailers because they were built with axles rated for 3000 lbs instead of the required 3500 lbs, which may affect handling.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0723-2016·2016-03-16

    Land O Lakes Margarine Cups Recalled for Missing Allergen Labeling

    Ventura Foods LLC is recalling Land O Lakes margarine cups because they were distributed without labels, failing to disclose milk and soy allergens.

    Product
    Land O Lakes, Fresh Buttery Taste Spread, 48% Vegetable Oil Spread, A product of Land O'Lakes Inc. Arden Hills, MN. Packaged in 5 gram plastic cups.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1047-2016·2016-03-16

    Gi Supply Recalls Large Volume Paracentesis Kits Due to Missing Clamp

    Gi Supply is recalling Large Volume Paracentesis Kits because the pinch clamp on the RP Bag may be missing, posing a splash hazard to users.

    Product
    Large Volume Paracentesis Kit is packaged in a thermaformed tray which contains slots and snap-in holders for most components. Packed sterile in Tyvek bag. Catalog #: GIS-28 Lot #: 61442434 Expiration Date: 2018/04
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Drugs)·D-0741-2016·2016-03-16

    Hartley Medical Center Pharmacy Recalls Morphine Sulfate Combination Vials

    Hartley Medical Center Pharmacy is recalling Morphine Sulfate, Sufentanil Citrate, and Bupivacaine HCL vials due to a lack of assurance of sterility.

    Product
    Morphine Sulfate 9 mg/ml/Sufentanil Cit 180 mcg/ml/Bupivacaine HCL 33 mg/ml, vol. 20 ml vial, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0719-2016·2016-03-16

    Whole Foods Market Brownies Recalled Due to Metal Shavings

    Whole Foods Market is recalling Crazy for Cream cheese Brownies because metal shavings were found around the perimeter of the product.

    Product
    Whole Foods Market Crazy for Cream cheese Brownie; Sold as single (4 oz.) and 4-pack (15 oz.) Ingredients: unbleached wheat flour, cocoa, vanilla, sugar, butter (pasteurized cream, salt), eggs, cream cheese (pasteurized milk and cream cheese culture, salt, xanthan and or…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1076-2016·2016-03-16

    BD Intelliport Medication Management System Sensor Recalled for Sterility Concerns

    Becton Dickinson is recalling 250 units of the BD Intelliport Medication Management System Sensor because the sterility of the product cannot be assured, posing an increased risk of infection.

    Product
    BD Intelliport Medication Management System Sensor The system is indicated for use by healthcare professionals in a hospital or medical center setting with patients who are receiving manually administered bolus intravenous injections as part of their care to facilitate…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0716-2016·2016-03-16

    Whole Foods Market Raspberry Brownies Recalled for Metal Shavings

    Whole Foods Market is recalling Raspberry Brownies sold in California after a customer found metal shavings around the product.

    Product
    Whole Foods Market Raspberry Brownie; sold as a single item (2. oz.) or a 4 pack (15 oz.); Ingredients: Unbleached wheat flour, sugar, butter (pasteurized cream, salt), eggs, cocoa, vanilla, raspberry preserves (raspberries, sugar, fruit pectin, citric acid), baking soda…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1068-2016·2016-03-16

    Bard Denali Filter Delivery System Recalled for Cracking Stop Cocks

    Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.

    Product
    Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of recurrent pulmonary embolism via placement in the vena cava.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1065-2016·2016-03-16

    Philips Respironics Recalls Trilogy and Garbin Ventilators Due to Software Issue

    Philips Respironics is recalling approximately 104,508 Trilogy and Garbin ventilators due to a software issue. The recall covers units distributed nationwide and internationally.

    Product
    Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation.
    Category
    Medical Device
    Distribution
    Distributed nationwide