The Recall Desk

Hazard

Foreign Object recalls

1,195 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,195
Critical
24
Severe
226
Most recent
2026-10-21

Of the 1,195 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 226 (19%) are Severe.

Which agencies issued them

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.

1176–1195 of 1195

  • HighFDA (Devices)·Z-1894-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Kits Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannula kits because a foreign substance on the cannula tips can be dislodged during use.

    Product
    CPB CATHETER KIT-DR BARTLES Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannula Kits Due to Foreign Substance

    Terumo is recalling Sarns Cardioplegia Cannula Kits because a foreign substance was found on the inner surface of some cannula tips that could be dislodged.

    Product
    CPB CATHETER KIT-DR GERHARDT Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1882-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that could dislodge.

    Product
    X-COATED TRANSPLANT PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1885-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.

    Product
    MAYO MN XCOATED 3/8X1/2 AV Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1881-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannula Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulae because a foreign substance was found on the inner surface of some tips that could be dislodged.

    Product
    XC HEART/LUNG PACK W/SX25RX Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1887-2012·2012-07-04

    Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.

    Product
    X-COATED H/L PK W/FX15RW40 Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1648-2012·2012-07-04

    Bay Valley Foods Recalls Macaroni and Cheese for Metal Fragments

    Bay Valley Foods is voluntarily recalling Kroger Macaroni & Cheese Three Cheese because the seasoning blend may contain small metal fragments.

    Product
    Kroger, Macaroni & Cheese Three Cheese, NET WT 7.25 OZ (205 g), UPC 1111085146, Distributed by The Kroger Co., Cincinnati, OH 45202.
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-1880-2012·2012-07-04

    Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance

    Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance on the inner surface of the tips can be dislodged during use.

    Product
    INDIANA/OHIO HEART Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1518-2012·2012-06-27

    Kerry Foods Recalls Sour Cream and Chives Product Due to Metal Fragments

    Kerry Foods is voluntarily recalling Sour Cream & Chives products contaminated with metal fragments. The recall covers 106 bags distributed across 15 US states, Canada, and Chile.

    Product
    KERRY, SOUR CRM & CHIVES 0989 S37SCC, CONTAINS MILK, , Item #I0989.465 , Net Wt 50 Lb (22.68Kg)
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-1509-2012·2012-06-27

    Kerry Foods Recalls Mac Sauce Mix Due to Metal Fragment Contamination

    Kerry Foods is voluntarily recalling Mac 7 CHS Sauce Mix because it is contaminated with metal fragments.

    Product
    KERRY, MAC 7 CHS SAUCE MIX 723357 CH723357, CONTAINS MILK, WHEAT, Item # 723357.859, Net Wt 1600 Lb (725.69 Kg)
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-1534-2012·2012-06-27

    Kerry Foods Recalls Meloblend 1048 Due to Metal Fragment Contamination

    Kerry Foods is voluntarily recalling Meloblend 1048, a lactic acid product, because it is contaminated with metal fragments.

    Product
    KERRY, MELOBLEND 1048, 95317, CONTAINS MILK, Item # I7067.465, Net Wt 50 Lb (22.68Kg)
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-1524-2012·2012-06-27

    Kerry Foods Recalls Lactic Acid Products Due to Metal Fragment Contamination

    Kerry Foods is voluntarily recalling lactic acid-containing products, including BATTER G3668, because they are contaminated with metal fragments.

    Product
    KERRY, BATTER G3668, 1520374, CONTAINS MILK AND WHEAT, Item #G3668.MC1, Net Wt 50 Lb (22.68Kg)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-1837-2012·2012-06-27

    Terumo Recalls Sarns Flexible Arterial Cannula Due to Foreign Substance

    Terumo CVS is recalling Sarns Flexible Arterial Cannulas because a foreign substance found on the connector surface can be dislodged during use.

    Product
    SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) WITH 3/8" CONNECTOR,SUTURE RING, 9.5" (24 CM) LONG. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1839-2012·2012-06-27

    Terumo Recalls Sarns High-Flow Aortic Arch Cannula Due to Foreign Substance

    Terumo is recalling Sarns High-Flow Aortic Arch Cannulae because a foreign substance was found on the outer surface of some connectors.

    Product
    24FR FLEX ART CANN NON STERILE. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1484-2012·2012-06-27

    Kerry Foods Recalls Lasagna Seasoning Contaminated with Metal Fragments

    Kerry Foods is voluntarily recalling Lasagna Sklt Seas 10078 due to contamination with metal fragments. The product was distributed in 15 US states and two countries.

    Product
    KERRY, LASAGNA SKLT SEAS 10078, SE10078, CONTAINS MILK, Item # I10078.859, Net Wt 1600 Lb (725.69Kg)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-1841-2012·2012-06-27

    Terumo Recalls Sarns High-Flow Aortic Arch Cannula Kits Due to Foreign Substance

    Terumo CVS is recalling Sarns High-Flow Aortic Arch Cannula kits because a foreign substance was found on the outer surface of some connectors.

    Product
    CUSTOM CPB CATHETER KIT-DR. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1492-2012·2012-06-27

    Kerry Foods Recalls Parmesan Blend Due to Metal Fragment Contamination

    Kerry Foods is voluntarily recalling Parmesan Blend products because they are contaminated with metal fragments. The affected items were distributed in 15 US states and two countries.

    Product
    Kerry, PARMESAN BLEND 720068 CH720068, CONTAINS MILK, WHEAT, Item # 720068.607, Net Wt 1000 Lb (453.556 Kg)
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Food)·F-1521-2012·2012-06-27

    Kerry Foods Recalls Lactic Acid Products Due to Metal Fragment Contamination

    Kerry Foods is voluntarily recalling lactic acid products contaminated with metal fragments. The affected items were distributed in 15 US states, Canada, and Chile.

    Product
    KERRY, KF # 11605R, CONTAINS MILK, Item #B18648.02 , Net Wt 50 Lb (22.68Kg)
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Drugs)·D-1381-2012·2012-06-20

    Endo Pharmaceuticals Recalls Endocet Tablets Due to Foreign Tablet Contamination

    Endo Pharmaceuticals is recalling specific bottles of Endocet 10 mg/650 mg tablets because some contained mixed 10 mg/325 mg tablets.

    Product
    Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only, Manufactured for: Endo Pharmaceuticals Inc., Chadds Ford, PA, By: Novartis, Lincoln, NE 68501; NDC 60951-797-70.
    Category
    Drug
    Distribution
    Distributed nationwide