The Recall Desk

Hazard

Foreign Object recalls

1,189 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,189
Critical
24
Severe
202
Most recent
2026-09-09

Of the 1,189 foreign object recalls we have scored against our rubric, 24 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 202 (17%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all foreign object recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

376–400 of 1189

  • HighFDA (Devices)·Z-0801-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical is recalling BriteBlade Pro laryngoscope blades because internal components may become loose and enter the patient's mouth.

    Product
    BriteBlade Pro Single-Use Fiber Optic Mac 3, CE01120, Do Not Re-use, Rx Only, REF 040-713U, Sterile EO, Qty 10, (01)15055788723001 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the vocal cords and the glottis by insertion into the oral
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0802-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal spring, washer, and bearing components may become loose and separate from the device.

    Product
    BriteBlade Pro Single-se Fiber Optic Miller 2, CE 0120, Do not Re-use, Rx Only, REF, 040-722U, Sterile EO, Qty 10, (01) 15055788722783 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the vocal cords and the glottis by insertion into the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0803-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal spring, washer, and bearing components may become loose and separate from the device.

    Product
    BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3, CE 0120, Do not Re-use, Rx Only, REF, 040-333U, Sterile EO, Qty 10, (01)15055788724138(17)230801(10)180900072 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the vocal cords an
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0483-2020·2020-01-15

    Nestle Toll House Turtle Cookie Bars Recalled for Rubber Pieces

    Nestle Toll House Ultimate Turtle Delight Cookie Bars are being recalled due to the potential presence of food-grade rubber pieces.

    Product
    Nestle Toll House Ultimate Turtle Delight Cookie Bar (16oz), UPC 050000009282
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0468-2020·2020-01-15

    Nestle Toll House Cookie Dough Recalled for Potential Rubber Pieces

    Gerber Products Company is recalling Simply Delicious Nestle Toll House Chocolate Chip Cookie Dough due to the potential presence of food-grade rubber pieces.

    Product
    Simply Delicious Nestle Toll House Chocolate Chip Cookie Dough (18oz), UPC 050000688760
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0471-2020·2020-01-15

    Nestle Toll House Chocolate Chip Chub Recalled for Rubber Pieces

    Gerber Products Company is recalling Nestle Toll House Chocolate Chip Chub due to potential food-grade rubber pieces.

    Product
    Nestle Toll House Chocolate Chip Chub (30oz), UPC 050000274444
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0489-2020·2020-01-15

    Nestle Toll House Oatmeal Raisin Cookie Bars Recalled for Rubber Pieces

    Gerber Products Company is recalling Nestle Toll House Oatmeal Raisin Cookie Bars due to the potential presence of food-grade rubber pieces.

    Product
    Nestle Toll House Oatmeal Raisin Cookie Bar (16.5oz), UPC 050000062195
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0481-2020·2020-01-15

    Nestle Toll House Cookie Dough Bars Recalled for Potential Rubber Pieces

    Gerber Products Company is recalling Nestle Toll House Triple Chip Cookie Dough Bars due to the potential presence of food-grade rubber pieces.

    Product
    Nestle Toll House Triple Chip Cookie Dough Bar (16oz), UPC 050000856237
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0488-2020·2020-01-15

    Nestle Toll House Sugar Cookie Bar Recalled for Rubber Pieces

    Gerber Products Company is recalling Nestle Toll House Sugar Cookie Bars due to the potential presence of food-grade rubber pieces.

    Product
    Nestle Toll House Sugar Cookie Bar (16.5oz), UPC 050000622443
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0474-2020·2020-01-15

    Nestle Toll House Chocolate Chip Tub Recalled for Rubber Pieces

    Gerber Products Company is recalling Nestle Toll House Chocolate Chip Tubs due to the potential presence of food-grade rubber pieces.

    Product
    Nestle Toll House Chocolate Chip Tub (36oz), UPC 050000622641
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0480-2020·2020-01-15

    Nestle Toll House Pinch of Grinch Cookie Dough Recalled for Rubber Pieces

    Gerber Products Company is recalling Nestle Toll House Pinch of Grinch Cookie Dough due to the potential presence of food-grade rubber pieces.

    Product
    Nestle Toll House Pinch of Grinch Cookie Dough (14oz), UPC 050000896639
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0653-2020·2019-12-25

    AuroMedics Recalls Gabapentin Capsules Due to Foreign Tablet Presence

    AuroMedics Pharma LLC is recalling specific lots of Gabapentin Capsules because a Losartan/HCTZ tablet was found in the bottles.

    Product
    Gabapentin Capsules, USP 100 mg, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810, NDC 65682-198-99
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0696-2020·2019-12-25

    Smith & Nephew Recalls PROFIX Mallets Due to Tip Detachment Risk

    Smith & Nephew is recalling 1,371 PROFIX Mallets because the poly tip may detach during surgery, potentially releasing particles into the surgical field.

    Product
    smith&nephew PROFIX Mallet, 750 GRAMS, REF 71512452 - Product Usage: The PROFIX Mallet is a reusable surgical instrument used to tap instruments or implants during knee or hip surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0693-2020·2019-12-25

    Medtronic Affinity Arterial Filter Recalled for Excess Plastic Flash

    Medtronic is recalling 24 units of Affinity 38um Arterial Filters due to excess plastic flash above the outlet port.

    Product
    Medtronic Affinity, 38um Arterial Filter, Catalog number REF 351
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0576-2020·2019-12-18

    Jubilant Cadista Recalls Amantadine Hydrochloride Tablets Due to Foreign Object

    Jubilant Cadista Pharmaceuticals is recalling 1,824 bottles of Amantadine Hydrochloride Tablets because a foreign object was found in a single tablet.

    Product
    Amantadine Hydrochloride Tablets, 100 mg, 100-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA; NDC 59746-699-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0330-2020·2019-12-18

    Breakstones Cottage Cheese Recalled for Potential Plastic and Metal Contamination

    Kraft Heinz is recalling Breakstones 4% Milkfat Small Curd Cottage Cheese due to the potential presence of red plastic and metal pieces introduced during production.

    Product
    Breakstones 4% Milkfat Small Curd Cottage Cheese, in 24 oz. Plastic Tub, with UPC 0 21000 12284 4, 12 packages per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0233-2020·2019-12-18

    AC Culinary Group Recalls Chef Pineiro's Sofrito con Albahaca Due to Metal Filament

    AC Culinary Group LLC is recalling Chef Pineiro's Sofrito con Albahaca in 12 oz and 32 oz sizes because a metal filament was found in the product and its raw materials.

    Product
    Chef Pineiro's Sofrito con Albahaca, with Basil, NET WT./PESO NETO 12 oz (340g) and NET WT./PESO NETO 32 oz (907g)
    Category
    Food
    Distribution
    1 state