The Recall Desk

State

American Samoa product recalls

73,833 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.

What the numbers show

Total
25
Critical
1
Severe
9
Most recent
2026-09-09

Of the 25 recalls naming American Samoa we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (36%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51476–51500 of 73858

  • HighFDA (Food)·F-0049-2016·2015-10-28

    JBN Chocolate Whey Superior Recalled for Undeclared Milk Allergen

    Nutrition Resource Services, Inc. is recalling JBN Chocolate Whey Superior because the product is not labeled as containing milk, a major allergen.

    Product
    JBN (Just Be Natural) Chocolate Whey Superior NET WT. 29.6 oz. (1.85 lb) 840g and NET WT. 88.9 oz. (5.55 lb) 2,520g - DIETARY SUPPLEMENT, packaged in plastic bottles, UPC codes: 655455020112, 655455001692, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0039-2016·2015-10-28

    JBN Growtein Protein Powder Recalled for Unlabeled Milk Allergen

    Nutrition Resource Services is recalling JBN Growtein Growth Protein because whey-based products are not labeled as containing milk.

    Product
    JBN (Just Be Natural) Growtein Growth Protein Vanilla Cream NET WT. 97 oz. (6 lb) 2750g - DIETARY SUPPLEMENT packaged in plastic bottles, UPC code: 655455001661, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN - Just Be Natural; INGREDIENTS: Whey…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0044-2016·2015-10-28

    JBN Unflavored Whey Isolate Recalled for Undeclared Milk Allergen

    Nutrition Resource Services, Inc. is recalling JBN Unflavored 100% Whey Isolate because the product is not labeled as containing milk, posing a risk to individuals with milk allergies.

    Product
    JBN (Just Be Natural) Unflavored 100% WHEY ISOLATE Enhanced Performance Nutrition; UPC code: 655455017594, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN -Just Be Natural NET WT. 27.5 oz. (1.72 lb) 780g - DIETARY SUPPLEMENT; packaged in plastic…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0054-2016·2015-10-28

    Hospira Recalls Amidate Etomidate Injection Due to Degradation Impurities

    Hospira Inc. is recalling 24,100 syringes of Amidate (Etomidate Injection) because stability testing confirmed out-of-specification degradation products.

    Product
    Amidate (Etomidate Injection, USP), 40 mg/20 mL (2 mg/mL), LifeShield, 20 mL, Glass Abboject Syringe with male luer lock adapter, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-8060-29
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0143-2016·2015-10-28

    ConForMIS iDuo Knee Replacement Recalled for Ethylene Glycol Residue

    ConforMIS, Inc. is recalling 12 units of the iDuo Knee Bicompartmental Knee Replacement System because they may contain small amounts of ethylene glycol residue.

    Product
    ConForMIS iDuo Knee Bicompartmental Knee Replacement System , iDUO G2, Right Medial Catalog Number: M57230600220 (US) M5723INT0600220 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0152-2016·2015-10-28

    Smiths Medical Recalls Port-A-Cath Needles Due to Incorrect Labeling

    Smiths Medical ASD, Inc. is recalling Port-A-Cath Plastic Hub Needles from Lot 46262 because the lid stock labels contain incorrect part numbers, descriptions, and images.

    Product
    PORT-A-CATH Plastic Hub Needles, 0.9mm (20G) x 19mm (3/4 in.) 90-degree. REF 21-2287-24 The Plastic hub PORT-A-CATH (PAC) needles are intended to access the implantable portal system for the purpose of infusion or withdrawal of fluids. These PAC needles can be used with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0147-2016·2015-10-28

    ConFormis iTotal Knee Replacement System Recalled for Ethylene Glycol Residue

    ConforMIS is recalling 110 units of the iTotal Posterior Stabilized Knee Replacement System because they may contain small amounts of ethylene glycol residue.

    Product
    ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL PS-IPOLY- IMPLANT KIT-LEFT and ITOTAL PS-IPOLY-IMPLANT KIT-RIGHT Catalog Number:TPS1111111
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0137-2016·2015-10-28

    Biomet Thinflap System Cases Recalled Due to Lid Opening Difficulty

    Biomet Microfixation is recalling 5 Thinflap System Cases because the lids require excessive force to open.

    Product
    Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0134-2016·2015-10-28

    Synthes Recalls Spinal Pedicle Fixation Rods Due to Finishing Process Error

    Synthes (USA) Products LLC is recalling 492 spinal pedicle fixation rods because they were produced using a bead blast process not identified in the manufacturing specification.

    Product
    5.0mm Unit Rod 270mm, 5.0mm Unit Rod 290mm, 5.0mm Unit Rod 310mm, 5.0mm Unit Rod 330mm, 5.0mm Unit Rod 350mm, 5.0mm Unit Rod 370mm, 5.0mm Unit Rod 390mm, 5.0mm Unit Rod 410mm, 5.0mm Unit Rod 430mm, 5.0mm Unit Rod 450mm; Orthosis, Spinal, Pedicle fixation Intended to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0144-2016·2015-10-28

    ConFormis iTotal CR Knee Replacement System Recalled for Ethylene Glycol Residue

    ConforMIS, Inc. is recalling 3 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.

    Product
    ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - LEFT ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - RIGHT Catalog Number: TCR1111111
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0035-2016·2015-10-28

    JBN Chocolate Whey Protein Powder Recalled for Missing Milk Labeling

    Nutrition Resource Services is recalling JBN Chocolate Confidence Nutritional Support for Bariatric Surgery because the whey protein product is not labeled as containing milk.

    Product
    JBN (Just Be Natural) Chocolate Confidence Nutritional Support for Bariatric Surgery 25G 100% WHEY ISOLATE; NET WT. 43.4 oz. (2.7 lb) 1,230g - packaged in plastic bottles, UPC code: 655455018225, DIETARY SUPPLEMENT MANUFACTURED BY NRS -Nutrition Resource Services, Inc.…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0146-2016·2015-10-28

    ConFormis iTotal CR Knee Replacement System Recalled for Ethylene Glycol Residue

    ConforMIS, Inc. is recalling 348 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.

    Product
    ConFormis iTotal CR Knee Replacement System- iTOTAL CR, Right Knee Catalog Number: M57250600020 (US) M5725INT0600020 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0153-2016·2015-10-28

    OneTray Sealed Sterilization Containers Recalled for Incorrect Labeling

    Innovative Sterilization Technologies LLC is recalling OneTray Sealed Sterilization Containers because the labels list the wrong steam sterilization time.

    Product
    OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization container used to steam sterilize medical devices
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0149-2016·2015-10-28

    Natus neoBLUE 3 Phototherapy System Recalled for Intensity Documentation

    Natus Medical is recalling 4,560 neoBLUE 3 Phototherapy systems because the instruction manuals did not accurately reflect the cleared intensity settings.

    Product
    Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy, Catalogue Part Number: 010066; Top Assembly Part Number: 001103
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0136-2016·2015-10-28

    Biomet Neuro Combo Set Case Lid Requiring Excessive Force Recalled

    Biomet Microfixation is recalling 37 Neuro Combo Set Cases because the lids require excessive force to open.

    Product
    Neuro Combo Set Case The cases hold surgical instrumentation in place during handling and storage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0140-2016·2015-10-28

    ConForMIS iUNI Knee Replacement Recalled for Ethylene Glycol Residue

    ConForMIS is recalling 6 units of the iUNI Unicondylar Knee Replacement System due to potential ethylene glycol residue.

    Product
    ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2, Right Lateral Catalog Number: M57220600240 (US) M5722INT0600240 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0139-2016·2015-10-28

    ConForMIS Knee Replacement System Recalled for Ethylene Glycol Residue

    ConforMIS, Inc. is recalling 71 units of the ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial due to potential small amounts of ethylene glycol residue.

    Product
    ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial Catalog Number: M57220600210(US) M5722INT0600210 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0053-2016·2015-10-28

    Donnatal Prescription Drug Recalled for Incorrect Ingredient Labeling

    Rx PAK is recalling Donnatal tablets because the label incorrectly lists Scopolamine Hydrocodone instead of Scopolamine Hydrobromide.

    Product
    DONNATAL — DONNATAL (PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V712000·2015-10-27

    Ford Recalls 2009-2010 Edge and Lincoln MKX for Fuel Tank Leak

    Ford is recalling 2009-2010 Edge and Lincoln MKX vehicles in 22 states and D.C. because salt water corrosion may cause the fuel tank to leak, increasing fire risk.

    Product
    FORD — FORD, LINCOLN EDGE, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V709000·2015-10-27

    Mercedes-Benz Recalls 2016 GLE450 and GLE63 Due to Drive Shaft Bolt Issue

    Mercedes-Benz is recalling 2016 GLE450 and GLE63 coupes because rear drive shaft bolts may loosen, causing the shaft to separate and the vehicle to stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE450, AMG GLE63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V711000·2015-10-27

    Mercedes-Benz Recalls Vehicles Due to Air Bag Control Unit Corrosion

    Mercedes-Benz is recalling 2008-2010 C300, C350, C63, and GLK350 vehicles because the air bag control unit may corrode and malfunction, potentially causing air bags to deploy unexpectedly or fail to deploy.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C63, GLK350, C300, C350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16018·2015-10-27

    LaRose Recalls Peanuts Flying Ace Ride-On Toys for Choking Hazard

    LaRose Industries is recalling Peanuts Flying Ace ride-on toys because blue hubcaps can detach, posing a choking hazard to young children.

    Product
    Peanuts Flying Ace Ride-On Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V710000·2015-10-27

    Ford Recalls 2016 E-350 and E-450 Vans for Trailer Brake Defect

    Ford is recalling 2016 E-350 and E-450 vans because the trailer brake controller may fail to actuate trailer brakes, increasing stopping distance and crash risk.

    Product
    FORD — FORD E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·132-2015·2015-10-26

    Adolf's Meat Products Recalls Assorted Deli Meat Due to Listeria Risk

    Adolf's Meat Products is recalling approximately 224 pounds of assorted deli meats produced in October 2015 due to possible Listeria monocytogenes contamination.

    Product
    Adolf's Meat Products — Adolf's Meat Products Recalls Assorted Deli Meat Due to Possible Listeria Adulteration
    Category
    Food
    Distribution
    Distributed nationwide