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.

39326–39350 of 50506

  • HighFDA (Devices)·Z-1280-2015·2015-03-25

    Mindray Recalls Passport V Monitors Due to Inaccurate Blood Pressure Readings

    Mindray is recalling 519 Passport V Monitors because the invasive blood pressure function may provide incorrect measurements.

    Product
    Passport V Monitor, Multiparameter Patient Monitor(with Arrhythmia Detection and Alarms) Intended for intra hospital use under the direct supervision of a licensed healthcare practitioner.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1272-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals

    Bard Access Systems is recalling 16,410 units of BD PosiFlush Saline Flush Syringes included in various device kits because open seals may impact product sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: PowerLoc Port Access Kit 19G x 1 in, PowerLoc Port Access Kit 20G x 1 in, , , PowerLoc Port Access Kit 20G x 1.5in, PowerLoc Port Access Kit 20G x 0.75in, , , PowerLoc Port Access Kit 22G x 1 in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1274-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals

    Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in certain catheter kits because open seals may compromise product sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: PowerGlide Midline Catheter Full Kit (20G) (8cm), PowerGlide Midline Catheter Maximal Barrier Tray (20G) (8cm), PowerGlide Midline Catheter Full Kit (20G) (10cm), The syringe is used to pre-flush…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1271-2015·2015-03-25

    Bard Access Systems Recalls BD PosiFlush Saline Syringes Due to Open Seals

    Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in various catheter kits because open seals may compromise product sterility.

    Product
    BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: Bard Poly Midline 3F Full Tray (Single-Lumen) (with Microintroducer), Bard Poly Midline 3F Maximal Barrier Tray (Single-Lumen), Bard Poly Midline 4F Maximal Barrier Tray (Single-Lumen) (with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1444-2015·2015-03-25

    Mint Cream Eggs Recalled for Missing Allergen Labeling

    Chris A Papas & Son Co is recalling Mint Cream Eggs because the labels fail to declare soy and Yellow #5, which are known allergens.

    Product
    Mint
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·15E024000·2015-03-25

    Gillig Recalls One Recaro Bus Driver Seat Due to Seat Belt Defect

    Gillig is recalling one Recaro bus driver seat because a tether bar may interfere with the seat belt locking mechanism, increasing injury risk in a crash.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1270-2015·2015-03-25

    GE Healthcare Ventilators Recalled for Caster Mounting Hardware Failure Risk

    GE Healthcare is recalling specific ventilator models due to a potential failure of the caster mounting hardware that could cause the device to fall or tip over.

    Product
    GE Healthcare Engstrom Carestation, Engstrom Pro, Cart Only S/5 EC. GE model numbers 1505-8538-000, 1505-9000-000, and 1505-9003-000. Ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1445-2015·2015-03-25

    Peanut Butter Recalled for Missing Allergen Labeling

    Chris A Papas & Son Co is recalling Peanut Butter because the labels fail to declare soy and Yellow #5, which are known allergens.

    Product
    Peanut Butter
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1416-2015·2015-03-25

    Wal-Mart Sock It To Me Crème Cake Recalled for Undeclared Pecans

    Benson's Old Home Kitchens is recalling Wal-Mart private label Sock It To Me Crème Cakes because they contain undeclared pecans, a major food allergen.

    Product
    Wal-Mart private label "the Bakery baked with pride," Sock It To Me Cr¿me Cake, Net Wt. 32oz (2lb) 907g, (packed in a rigid clear plastic dome), Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716.
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1433-2015·2015-03-25

    Rill Foods Recalls Shoshone Falls Black Bean Soup Due to Peanut Contamination

    Rill Foods is recalling Shoshone Falls Black Bean Soup because the cumin used may be contaminated with peanut protein.

    Product
    The product label reads in part "***Shoshone Falls Black Bean Soup*** Rill Foods***NET WT. 13 OZ.***" or "*** NET WT. 12.5 OZ.***"The product is packaged in a clear flexible laminate bag with a yellow card stock topper label which has black/brown print. Case label is a white…
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1269-2015·2015-03-25

    Baxter MiniCap with Povidone-Iodine Solution Recalled for Sponge Defects

    Baxter Healthcare is recalling MiniCap with Povidone-Iodine Solution units for hemodialysis because the product may have separating or protruding sponges.

    Product
    MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1278-2015·2015-03-25

    Puritan Absorbent Foam Tipped Applicator Recall Due to Shaft Breakage

    Puritan Medical Products is recalling sterile absorbent foam tipped applicators because the shafts may break, preventing adequate patient specimen collection.

    Product
    Puritan absorbent foam tipped applicator; Catalog Number 25-1406 1 PF BT. Sterile absorbent foam tipped applicator used to apply medication or to obtain specimens from a patient.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1279-2015·2015-03-25

    GE Healthcare Recalls Nuclear Medicine Systems Due to Collimator Detachment Risk

    GE Healthcare is recalling 472 nuclear medicine systems worldwide because a collimator may fall off during rotation. No injuries have been reported.

    Product
    GE Healthcare Millennium VG, Discovery VH and VariCam Nuclear Medicine systems, all configurations. Product Usage: The intended use of the system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body, using…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1432-2015·2015-03-25

    Rill Foods Recalls Chicken Chowder Due to Potential Peanut Contamination

    Rill Foods is recalling Buena Mexi Chicken Chowder because the cumin used may be contaminated with peanut protein.

    Product
    The product label reads in part "***Buena Mexi Chicken Chowder *** Rill Foods***NET WT. 6.7 OZ.***" or "*** NET WT. 3.35 OZ.***"The product is packaged in a clear flexible laminate bag with a green card stock topper label which has white print. Case label is a white sticker…
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1295-2015·2015-03-25

    Transonic Hemodialysis Monitor Recall Due to Inaccurate Flow Measurements

    Transonic Systems Inc is recalling Hemodialysis Monitors that may display zero or low flow values, preventing accurate measurements during dialysis.

    Product
    Transonic Hemodialysis Monitor, Model HD03 -- Product Usage: The Hemodialysis Monitor is intended for use by trained medical personnel to measure delivered blood flow, vascular access recirculation, vascular access blood flow and cardiac output on patients receiving…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1299-2015·2015-03-25

    Fisher Brand Infant Heel Warmers Recalled for Burn Risk

    CooperSurgical is recalling Fisher Brand Gel and Liquid Infant Heel Warmers because products without expiration dates pose a remote potential for minor burns.

    Product
    Fisher Brand Gel Infant Heel Gel Warmers, Cat. No.: 22-024647 Fisher Brand Liquid Infant Heel Warmer, Cat. No: 22-024646 To provide gentle heat to increase blood flow and enhance infant blood sample collection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1451-2015·2015-03-25

    Goya Black Bean Soup Recalled for Possible Peanut Contamination

    Goya Foods is recalling 29-ounce cans of Black Bean Soup and Kirby brand black beans due to possible peanut contamination.

    Product
    Goya Black Bean Soup Net Wt. 29 oz. Goya Foods, Secaucus, NJ 07096 Product of Dominican Republic UPC 0 4133102081 7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V175000·2015-03-25

    Ford Recalls 2011-2015 F-Series Trucks With Emergency Vehicle Packages

    Ford is recalling 6,322 model year 2011-2015 F-350, F-450, and F-550 trucks equipped with ambulance or fire engine packages due to a software defect that may cause the engine to shut down unexpectedly.

    Product
    FORD — FORD F-550 SD, F-450 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1292-2015·2015-03-25

    Baxter HomeChoice Pro APD System Recalled for Occluder Defect

    Baxter Healthcare is recalling 75 HomeChoice Pro APD systems because the occluder may have sharp edges or separate, causing system errors or therapy termination.

    Product
    The HomeChoice Pro APD System is a peritoneal dialysis system. The HomeChoice Pro Automated Personal Cycler peritoneal dialysis system is intended for automatic control of dialysate solution exchange in the treatment of pediatric and adult renal failure patients undergoing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1286-2015·2015-03-25

    Smiths Medical Recalls CADD Medication Cassette Reservoirs Due to Leak Risk

    Smiths Medical is recalling specific lots of 50mL CADD Medication Cassette Reservoirs because they may leak at the sealing area. No serious injuries or deaths have been reported.

    Product
    CADD" Medication Cassette Reservoir, 50mL, REF 21-7001-24 & 21-7301-24, Sterile EO, Rx only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V171000·2015-03-24

    Ford Recalls 2011-2013 Explorers for Door Handle Spring Defect

    Ford is recalling 2011-2013 Explorers because an interior door handle spring may unseat, preventing the handle from returning to its stowed position. This could cause the door to unlatch in a side impact crash.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide