The Recall Desk

State

American Samoa product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49926–49950 of 73852

  • SevereFDA (Food)·F-0600-2016·2016-02-24

    Uncle Buck's Fish Batter Mix Recalled for Undeclared Milk Ingredient

    BlendTech Inc is recalling Uncle Buck's Fish Batter Mix Original because it contains an undeclared milk ingredient. The product was distributed nationwide.

    Product
    Uncle Buck's Fish Batter Mix Original, packaged in 22 oz. (623 g) plastic bottles, bottle lot #09241505, UPC 09229725284 and packed 12 bottles/case. Bottles were shipped in cases under lot #09241506 and lot #09241507. Produced and Packaged in the USA for Bass Pro Shops By…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0805-2016·2016-02-24

    Varian Eclipse Treatment Planning System Recall for Dose Calculation Error

    Varian Medical Systems is recalling Eclipse Treatment Planning System versions 11, 13.0, 13.5, and 13.6 due to a dose calculation error that may result in unintended radiation exposure.

    Product
    Eclipse Treatment Planning System versions 11, 13.0, 13.5 and 13.6; Model number: H48; Product Usage: The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients with malignant or benign diseases. Eclipse TPS is used to plan…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0821-2016·2016-02-24

    Medtronic Recalls Endo GIA Ultra Universal 12 mm XL Stapler Handles

    Medtronic is recalling 327,797 Endo GIA Ultra Universal 12 mm XL Stapler Handles worldwide because the staplers may fail to fire or the articulating lever may disengage during surgery.

    Product
    Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Ref: EGIAUXL Product Usage: The Endo GIA Ultra Universal Short, Endo GIA Ultra Universal and Endo GIA Ultra Universal XL staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V106000·2016-02-24

    Temsa Recalls 2016 TS45 and TS35C Buses for Front Control Arm Defect

    Temsa is recalling 70 model year 2016 TS45 and TS35C buses because front lower control arm housings may crack. This defect could cause a loss of steering and increase the risk of a crash.

    Product
    TEMSA — TEMSA TS45, TS35C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0663-2016·2016-02-24

    Medline Acetaminophen Tablets Recalled for Incorrect Strength Labeling

    Medline Industries is recalling 325 mg acetaminophen tablets that are actually 500 mg due to a labeling error.

    Product
    ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets, 325 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-642-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·16109·2016-02-24

    England's Stove Works Recalls Smartstove Pellet Stoves for Laceration Hazard

    England's Stove Works is recalling about 2,300 Smartstove freestanding pellet stoves because ash accumulation can cause the door glass to break, posing a laceration hazard.

    Product
    Smartstove freestanding pellet stoves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0807-2016·2016-02-24

    Bio-Rad EVOLIS Microplate System Recalled for Plate Transport Hazard

    Bio-Rad is recalling 278 EVOLIS Microplate Systems because a low fluid alarm could cause the plate transport to continue running, pushing plates off the transporter.

    Product
    EVOLIS Microplate System, Catalog # 89601. Part number 89788 for the EVOLIS Operator's Manual. in vitro diagnostic Product Usage: EVOLIS Microplate System is a 4 plate fully integrated microplate processing system designed for use with multiple EIA assays.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0810-2016·2016-02-24

    Philips recalls actuator assemblies for angiographic x-ray monitor ceiling suspension systems

    Philips is recalling actuator assemblies for angiographic x-ray monitor ceiling suspension systems because the actuator can detach, causing the monitor carriage to drop.

    Product
    Actuator for angiographic x-ray monitor ceiling suspension system. Actuator short Assy: THC8AWDS-121 and Actuator long Assy: THC8AWDS-122 used with the following products: 722001 Allura Xper FD 10 C; 722003 Allura Xper FD10; 722005 Allura Xper FD10/10; 722006 Allura Xper FD20…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0817-2016·2016-02-24

    Nihon Kohden MEE-1000A Neuromaster Accessories Recalled for Defective Circuit Boards

    Nihon Kohden America Inc is recalling MEE-1000A Neuromaster accessories due to defective printed circuit boards that failed to prevent unintentional current flow.

    Product
    MEE-1000A Neuromaster, Model No. Accessories: MS-110B (Electric Stimulation), MS-120BK (Current Stimulator Box) JB-116B, JB-132B (Amplifiers) Electromyography. (EMG)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0814-2016·2016-02-24

    CareFusion Recalls Jadak Barcode Scanners for Pyxis Anesthesia Systems

    CareFusion 303, Inc. is recalling 9,345 Jadak Barcode Scanners used with Pyxis Anesthesia systems because they may transmit incorrect medication information to the dispensing system.

    Product
    Jadak Barcode Scanner, Part No. 350587-32, 350587-41, 351377-32. Product Usage: An accessory for the Pyxis Anesthesia ES system and Pyxis Anesthesia system 4000 stations. The Jadak Barcode Scanner is used to scan medication labels during refill of the Pyxis Anesthesia ES…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V105000·2016-02-24

    Isuzu Recalls 2016 Trucks Due to Certification Label Errors

    Isuzu is recalling certain 2016 NPR-HD, NPR-XD, NQR, and NRR trucks because typographical errors on the certification label may prevent accurate vehicle loading and maintenance.

    Product
    ISUZU — ISUZU NPR HD, NPR XD, NQR, NRR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0808-2016·2016-02-24

    Leica Bond Polymer Refine Red Detection Kits Recalled for Staining Errors

    Leica Microsystems is recalling Bond Polymer Refine Red Detection kits due to a manufacturing error that may cause inadequate staining.

    Product
    Bond Polymer Refine Red Detection DS9390 kits. The common name of the device is detection system for in vitro diagnostic use. The Intended Use states that Bond Polymer Refine Red Detection is a biotin-free, polymeric alkaline phosphatase (AP)-linker antibody conjugate system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0665-2016·2016-02-24

    Bonita Pharmaceuticals Recalls Menthocin Patch with Lidocaine-Strong

    Bonita Pharmaceuticals is recalling Menthocin Patch with Lidocaine-Strong because it was marketed without an approved NDA or ANDA.

    Product
    Menthocin Patch with Lidocaine-Strong (Menthol 5%, Capsaicin 0.0375%, Methyl Salicylate 20%, Lidocaine 0.5%), packaged in a box 15 patches, RX Only, Manufactured for Bonita Pharmaceuticals LLC 6380 Commerce Drive Westland, MI 48185-9120, USA NDC 53598-0012-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0720-2016·2016-02-24

    Dr. Reddy's Recalls Paricalcitol Capsules Due to Breakage and Leakage

    Dr. Reddy's Laboratories is recalling Paricalcitol capsules due to reports of breakage and leakage. The recall covers 4,383 bottles distributed nationwide.

    Product
    PARICALCITOL — PARICALCITOL (PARICALCITOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0812-2016·2016-02-24

    C.R. Bard Recalls Toomey Syringes Due to Open Package Seal

    C.R. Bard is recalling 15,400 units of 70cc Toomey Syringes because a customer reported an open package seal.

    Product
    REF 0038460 Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters, Single Use, Rx Only, Latex Free, 50 units. Product Usage: Product is intended for Resectoscope irrigation, catheter irrigation and Foley catheter inflation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V102000·2016-02-23

    Kawasaki Recalls 2016 Ninja ZX-10R Motorcycles for Steering Bolt Defect

    Kawasaki is recalling 544 model year 2016 Ninja ZX-10R motorcycles because steering damper bracket mounting bolts may break, potentially interfering with steering and increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA ZX-10R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V100000·2016-02-23

    Blue Bird Recalls 2008-2009 Vision School Buses for Fire Risk

    Blue Bird is recalling 733 model year 2008-2009 Vision school buses because a wiring defect may cause the battery cable to overheat, melt, and create a fire risk.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V101000·2016-02-23

    Blue Bird Recalls 2009 Vision Transit Buses for Electrical Fire Risk

    Blue Bird is recalling 2009 Vision transit buses with Caterpillar C707 engines because a wiring defect may cause the battery cable to overheat, melt, and create a fire hazard.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V103000·2016-02-23

    Thomas Built Buses Recalls Minotour School Buses for Lighting Defect

    Daimler Trucks North America is recalling 2012-2017 Thomas Built Buses Minotour school buses because a body control module failure may cause loss of exterior lighting or windshield wipers.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·020-2016·2016-02-23

    Ajinomoto Recalls Pork Dumplings Misbranded as Beef

    Ajinomoto Windsor Inc. is recalling approximately 6,000 pounds of Shirakiku Gyoza Dumplings labeled as beef but containing undeclared pork.

    Product
    Ajinomoto Windsor Inc. — Recall Notification Report 020-2016 (Pork Products )
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V099000·2016-02-19

    Mack Trucks Recalls 2012-2016 Models for Driveshaft Cap Nut Defect

    Mack Trucks is recalling 33,981 model year 2012-2016 trucks because a cap nut may loosen, causing the driveshaft to disconnect and increasing crash risk.

    Product
    MACK — MACK TITAN (TD), PINNACLE (CHU), TERRAPRO (LEU), PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide