The Recall Desk

State

Northern Mariana Islands product recalls

73,833 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total
23
Critical
0
Severe
18
Most recent
2026-09-23

Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57576–57600 of 73856

  • ModerateFDA (Devices)·Z-2081-2014·2014-07-30

    AGFA DX-D 100 X-Ray System Recalled for Touch Screen Malfunction

    AGFA Corp. is recalling 216 DX-D 100 digital radiography systems because liquid contact with the touch screen may cause the device to incorrectly recognize user input and alter settings.

    Product
    AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality images to aid the physician with diagnosis. Systems can be used with MUSICA2 image processing to create radiographic images of the skeleton including skull…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2087-2014·2014-07-30

    Synthes Orthopedic Guide Blocks Recalled for Incorrect Labeling

    Synthes, Inc. is recalling 180 Guide Blocks for the Volar Distal Radius Plate System due to incorrect package labeling. The physical parts are correctly marked, but the packaging may identify the wrong side.

    Product
    Synthes Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius Plate System). Orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2196-2014·2014-07-30

    Country Life Liquid Calcium Magnesium Supplement Recalled for Particulates

    Country Life is recalling specific lots of its liquid calcium and magnesium dietary supplement because the product contains insoluble particulates that do not meet quality standards.

    Product
    Country Life TARGET MINS CALCIUM MAGNESIUM With Vitamin D3 Complex, WILD BLUEBERRY FLAVOR, LIQUID Dietary Supplement, 16 FL. OZ. (1 PINT) (472 mL), Product No. 2523, Bar Code 015794025238, and 32 FL. OZ. (1 QT) (944 mL), Product No. 2522, Bar code 015794025221 --- Manufactured…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2215-2014·2014-07-30

    Kraft Recalls Knudsen, Breakstone's, and Other Cottage Cheese Brands

    Kraft Foods is voluntarily recalling multiple cottage cheese brands due to ingredients not stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with mango topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2106-2014·2014-07-30

    Terumo CPB Catheter Kit Recalled for Loose Fiber Particulate

    Terumo CVS is recalling 125 CPB Catheter Kits because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    CPB Catheter Kit Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior vena cava.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2216-2014·2014-07-30

    Kraft Recalls Cottage Cheese Due to Improper Ingredient Storage

    Kraft Foods is voluntarily recalling specific cottage cheese products because ingredients were not stored at proper temperatures, creating a potential safety risk.

    Product
    Cottage cheese, 2% milkfat, with pineapple sold under the Breakstone's brand or Knudsen brand and packaged in a tray of 4 plastic containers each with a net weight of 4 oz. (113 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2097-2014·2014-07-30

    Terumo Recalls Sarns Malleable Venous Return Cannulae Due to Particulate

    Terumo CVS is recalling Sarns Malleable Venous Return Cannulae because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    Sarns Malleable Venous Return Cannulae 24, 28, 30, 32, 34, 36 & 40 Fr single stage with 3/8" & 1/2 flare with or without Xcoating Product Usage: The Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2105-2014·2014-07-30

    Terumo Recalls Sarns Soft-Flow Aortic Cannulae Due to Fiber Particulate

    Terumo CVS is recalling Sarns Soft-Flow Aortic Cannulae because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    Sarns Soft-Flow Aortic Cannulae 6.0mm, 7mm & 8mm angled and straight tip, suture bulb with or without Luer and/or Xcoating Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2102-2014·2014-07-30

    Terumo Dual-stage Venous Return Cannulae Recalled for Loose Fiber Particulate

    Terumo CVS is recalling specific lots of venous return cannulae used in heart surgery due to loose fiber particulate found during inspection.

    Product
    Terumo Dual-stage Venous Return Cannulae 28/38, 29/37, 32/40, 34/46, 36/46 & 36/51 Fr with 1/2" flare or connector Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2217-2014·2014-07-30

    Kraft Recalls Knudsen and Other Cottage Cheese Brands for Temperature Violations

    Kraft Foods is voluntarily recalling multiple cottage cheese brands produced in California because ingredients were not stored at proper temperatures.

    Product
    Low fat cottage cheese, 1.5% milkfat, with pineapple sold under the Knudsen brand packaged in plastic containers with a net weight of 16 oz. (1 lb.) 453 g.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2211-2014·2014-07-30

    Kraft Recalls Knudsen, Breakstone's, and Other Cottage Cheese Brands

    Kraft Foods is voluntarily recalling multiple cottage cheese brands due to ingredients not being stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with strawberry topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2104-2014·2014-07-30

    Terumo Recalls Three-stage Venous Return Cannulae Due to Loose Fiber Particulate

    Terumo Cardiovascular Systems is recalling specific lots of Three-stage Venous Return Cannulae because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    Terumo Three-stage Venous Return Cannulae 28 Fr with 3/8" flare, 30 Fr with 3/8" connector and 30 Fr with 3/8" flare. Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and inferior…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2210-2014·2014-07-30

    Kraft Recalls Knudsen, Breakstone's, and Other Cottage Cheese Brands

    Kraft Foods is voluntarily recalling multiple cottage cheese brands due to ingredients not being stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with peach topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2207-2014·2014-07-30

    Kraft Recalls Cottage Cheese Due to Temperature Storage Issues

    Kraft Foods is voluntarily recalling Knudsen, Breakstone's, Simply Kraft, and Daily Chef cottage cheese because ingredients were not stored at proper temperatures.

    Product
    Fat free cottage cheese sold under the Knudsen or Kraft brand and packaged in a plastic container with a net weight of 16 oz. (1 lb.) 453 g, a plastic container with a net weight of 24 oz. (1.5 lb.) 680 g, or a plastic container with a net weight of 32 oz. (2 lb.) 907 g.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2095-2014·2014-07-30

    Terumo Recalls Sarns Aortic Arch Cannulas Due to Loose Fiber Particulate

    Terumo CVS is recalling 120 units of Sarns Flexible Aortic Arch Cannulas because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    Sarns Flexible Aortic Arch Cannula 8.0mm with luer, 3/8" connector Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2213-2014·2014-07-30

    Kraft Recalls Knudsen and Other Cottage Cheese Due to Storage Issues

    Kraft Foods is voluntarily recalling multiple cottage cheese brands due to ingredients not being stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with blueberry topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2093-2014·2014-07-30

    Salter Labs Recalls Oxygen Masks Due to Incorrect Labeling

    Salter Labs is recalling 584 units of Model No. 8120-7 oxygen masks because the insert label incorrectly identifies the device as a non-rebreather instead of a partial rebreather.

    Product
    Oxygen Mask, Model No. 8120-7 Product Usage: Oxygen Mask, High Concentration partial rebreather, with 7 foot (2.1 m) supply tube, Elastic Strap Fixation, Single patient use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2212-2014·2014-07-30

    Kraft Recalls Knudsen and Other Cottage Cheese Brands Due to Storage Issues

    Kraft Foods is voluntarily recalling multiple cottage cheese brands produced in Tulare, CA, because ingredients were not stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with pineapple topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2101-2014·2014-07-30

    Terumo Recalls Sarns Venoatrial Cannulae Due to Loose Fiber Particulate

    Terumo CVS is recalling 3,040 Sarns Venoatrial Cannulae units because in-process inspections found loose fiber particulate exceeding specifications.

    Product
    Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Product Usage: The Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use. The Venous Return Cannula…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2103-2014·2014-07-30

    Terumo TenderFlow Pediatric Venous Cannulae Recalled for Loose Fiber Particulate

    Terumo CVS is recalling specific lots of TenderFlow Pediatric Venous Cannulae due to loose fiber particulate exceeding specifications found during inspection.

    Product
    Terumo TenderFlow Pediatric Venous Cannulae, 8, 10, 12, 14, 16, 18, 20, 22 & 24 Fr angled & straight tip, 1/4" & 3/8" flare, Product Usage: Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass surgery for dual cannulation of the superior and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2209-2014·2014-07-30

    Kraft Recalls Cottage Cheese Due to Temperature Storage Violations

    Kraft Foods is voluntarily recalling multiple brands of cottage cheese because ingredients were not stored at proper temperatures, creating a potential safety risk.

    Product
    Cottage cheese, 4% milkfat, sold under the Daily Chef, Knudsen, or Kraft brand and packaged in a plastic container with a net weight of 8 oz. (227 g), a plastic container with a net weight of 16 oz. (1 lb.) 453 g, a plastic container with a net weight of 24 oz. (1.5 lb.) 680 g…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2208-2014·2014-07-30

    Kraft Recalls Cottage Cheese Due to Improper Ingredient Storage

    Kraft Foods is voluntarily recalling cottage cheese sold under Breakstone's, Daily Chef, Knudsen, and Kraft brands because ingredients were not stored at proper temperatures.

    Product
    Low fat cottage cheese, 2% milkfat, sold under the Breakstone's brand, Daily Chef brand, Knudsen brand, or Kraft brand packaged in a tray of 4 plastic containers each with a net weight of 4 oz. (113 g), a tray of 8 plastic containers each with a net weight of 4 oz. (113 g), a…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2214-2014·2014-07-30

    Kraft Recalls Knudsen and Other Cottage Cheese Due to Temperature Storage Issues

    Kraft Foods is voluntarily recalling multiple cottage cheese brands produced in Tulare, CA, because ingredients were not stored at proper temperatures.

    Product
    Cottage Doubles - cottage cheese, 2% milkfat, with raspberry topping sold under the Knudsen brand and packaged in a plastic container with a net weight of 3.9 oz. (110 g).
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1444-2014·2014-07-30

    X-Gen Recalls Clonidine HCl Injection Due to Labeling Error

    X-Gen Pharmaceuticals is recalling Clonidine HCl Injection vials because the side label incorrectly states the drug strength.

    Product
    CLONIDINE — CLONIDINE (CLONIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1445-2014·2014-07-30

    Sandoz Recalls Orphenadrine Citrate Tablets for Dissolution Failures

    Sandoz Inc. is recalling Orphenadrine Citrate Extended Release Tablets because they failed dissolution specifications during stability testing.

    Product
    ORPHENADRINE CITRATE — ORPHENADRINE CITRATE (ORPHENADRINE CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide