The Recall Desk

Archive

April 2020 recalls

605 recalls were announced in April 2020.

What the numbers show

Critical
6
Severe
113
High
182
Moderate
294
Low
10

Of the 605 recalls this month scored against our rubric, 1% are Critical, 19% are Severe.

Which agencies issued them

601–605 of 605

  • ModerateFDA (Food)·F-0901-2020·2020-04-01

    Organic By Nature Supermeal Vanilla Chai Recalled for Unapproved Herbicide

    Organic By Nature is recalling L.O.V.E. Supermeal Vanilla Chai because it contains Organic Ground Flaxseed powder contaminated with the unapproved herbicide Haloxyfop.

    Product
    L.O.V.E. Supermeal Vanilla Chai: 1320g Plastic Bottle, 660g Bio Bag Terra Pouch; Finished Product Item #: 2910E, 2910, 2910-P65, 2911, 2911-P65 Platinum Health Europe, Netherlands, Purim Health Products, Rancho Dominguez, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0852-2020·2020-04-01

    Dean Foods Recalls Baskin Robbins Ice Cream Sandwiches for Undeclared Dyes

    Dean Foods is recalling Baskin Robbins Mint Chocolate Chip Ice Cream Sandwiches because they contain undeclared Yellow #5 and Blue #1 dyes.

    Product
    Baskin Robbins Mint Chocolate Chip, Ice Cream Sandwiches with Mint Ice Cream, Semi-Sweet Chocolate Chips & Chocolate Wafers 4 Pack; 4 3.5 FL OZ (104 mL) Sandwiches /14 FL OZ (414 mL)
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1571-2020·2020-04-01

    Bard PowerPort M.R.I. Implantable Port Catheter Recall for Incorrect Tunneler Tip

    Bard Peripheral Vascular Inc is recalling 878 PowerPort M.R.I. Implantable Port catheters because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.

    Product
    1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, REF: 1809600, UDI: (01)00801741027130 ; 2. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter Without Suture Plugs,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1565-2020·2020-04-01

    Cook Inc. Recalls Pericardiocentesis Sets Due to Incorrect Expiration Dates

    Cook Inc. is recalling 25 Pericardiocentesis Sets because the printed expiration dates are incorrect. The products were distributed to seven US states and Canada.

    Product
    Pericardiocentesis Set, Irrigation Catheter, Reference Part Number C-PCS-700-TORONT0-042997, Order Number G10643
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-1049-2020·2020-04-01

    FDA Recalls Colostat Homeopathic Remedy Due to Incorrect Labeling

    Grato Holdings, Inc. is recalling 659 bottles of Colostat homeopathic remedy because the indications on the product label are incorrect.

    Product
    COLOSTAT — COLOSTAT (RHAMNUS PURSHIANA, SPIGELIA ANTHELMIA, TARAXACUM OFFICINALE, CAJUPUTUM, HYDRASTIS CANADENSIS, ALUMINA, CINA, CINCHONA OFFICINALIS, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, MANDRAGORA OFFICINARUM, NUX VOMICA)
    Category
    Drug
    Distribution
    Distributed nationwide

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