The Recall Desk

Archive

October 2019 recalls

807 recalls were announced in October 2019.

What the numbers show

Critical
64
Severe
328
High
307
Moderate
88
Low
20

Of the 807 recalls this month scored against our rubric, 8% are Critical, 41% are Severe.

Which agencies issued them

801–807 of 807

  • LowFDA (Devices)·Z-2498-2019·2019-10-02

    Philips Recalls Two DigitalDiagnost C50 X-ray Systems for Missing Labels

    Philips Healthcare is recalling two DigitalDiagnost C50 stationary X-ray systems in Puerto Rico due to a missing label identified during recent evaluations.

    Product
    DigitalDiagnost C50, Stationary X-ray System
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-2557-2019·2019-10-02

    Randox Urinalysis Control Level 2 Recalled for Incorrect Leukocyte Range

    Randox Laboratories is recalling Randox Urinalysis Control Level 2 kits because the leukocyte range for the Siemens Multistix method was incorrect.

    Product
    Randox Urinalysis Control Level 2 (IVD) Ref: UC5034 - Product Usage: Product is intended for in vitro diagnostic use in the quality control of urine test strips.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2555-2019·2019-10-02

    Arrow International Recalls Central Venous Access Kits Due to Incorrect Banner Card

    Arrow International Inc is recalling 520 units of ARROW+gard Blue PSI Kit Cath-Gard central venous access devices because they may contain the incorrect banner card.

    Product
    8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard for use with 7.5 - 8 Fr.Catheters Product Code: CDC-29803-1A - Product Usage: The MACTM Two-Lumen Central Venous Access Device with ARROWg+ard Blue¿ permits venous access and catheter introduction to the central circulation. It m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0001-2020·2019-10-02

    Pfizer Recalls Ethosuximide Capsules Due to Incorrect Expiration Date Labeling

    Pfizer is recalling 7,824 bottles of ethosuximide capsules because the expiration date on the label is incorrect.

    Product
    ethosuximide capsules, USP, 250 mg, 100-count bottle, Rx Only, Distributed by: Greenstone LLC Peapack, NJ 07977 Made in Netherlands. NDC 59762-2250-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V692000·2019-10-01

    BMW Recalls 2017-2020 K 1600 Series Motorcycles for Transmission Defect

    BMW is recalling 2017-2020 K 1600 GT, GTL, and B motorcycles because transmission parts may not be hard enough, risking rear wheel lockup and crashes.

    Product
    BMW — BMW K1600B, K 1600 GTL, K 1600 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V690000·2019-10-01

    Jayco Recalls 2019-2020 Redhawk SE Motorhomes for Seatbelt Warning Defect

    Jayco is recalling 2019-2020 Redhawk SE motorhomes because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition, increasing crash injury risk.

    Product
    JAYCO — JAYCO REDHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide

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