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.

51151–51175 of 73858

  • HighFDA (Devices)·Z-0249-2016·2015-11-18

    Stryker Recalls Triathlon MIS Modular Distal Capture Instruments

    Stryker is recalling specific lots of Triathlon MIS Modular Distal Capture instruments because they may disassociate during use.

    Product
    Stryker Orthopaedics, MIS MODULAR DISTAL CAPTURE TRIATHLON MIS INSTRUMENTS, REF 6541-5-723, Lot AdminECR19205, Non-Sterile, The Triathlon MIS Distal Capture is used when a surgeon elects to use a capture for the distal femoral resection in a Triathlon primary MIS TKA. Once the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0245-2016·2015-11-18

    Teleflex Medical Recalls Roesch Flexi-Slip Endotracheal Tube Stylets

    Teleflex Medical is recalling Roesch Flexi-Slip Endotracheal Tube Stylets because the plastic coating may split or break off.

    Product
    R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip, Sterile, Rx only, Teleflex Medical.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0260-2016·2015-11-18

    GE Healthcare Recalls SIGNA PET/MR 3.0T Scanners for SAR Display Error

    GE Healthcare is recalling 17 SIGNA PET/MR 3.0T scanners because displayed SAR values may be lower than actual levels, potentially exceeding safety limits during head or neck scans.

    Product
    GE Healthcare, SIGNA PET/MR 3.0T. Product Usage: The SIGNA PET/MR system combines magnetic resonance diagnostic devices (MRDD) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high-resolution physiologic and anatomic information…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0258-2016·2015-11-18

    GE Healthcare Recalls Signa HDx 3.0T MRI Scanners for SAR Display Error

    GE Healthcare is recalling 350 Signa HDx 3.0T MRI scanners because displayed SAR values may be lower than actual head SAR levels, potentially exceeding safety limits.

    Product
    GE Healthcare, SIGNA HDx 3.0T. Product Usage: The GE Signa HDx MR system is a whole body magnetic resonance scanner for use as a diagnostic imaging device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0233-2016·2015-11-18

    Utah Medical Recalls Myelo-Nate CSF Sampling Kits Due to Seal Compromise

    Utah Medical Products is recalling 21,403 Myelo-Nate CSF Sampling Kits because an internal inspection found a compromised sterile seal on one side of the tray.

    Product
    Myelo-Nate CSF Sampling Kit, Neonatal/Pediatric cerebralspinal fluid sampling sterile tray, including a lumbar puncture needle, four collection vials, an iodine swabstick package, a fenestrated drape, a polylined drape, three gauze pads, and one spot bandage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0164-2016·2015-11-18

    C. O. Truxton Recalls Doxycycline Hyclate Tablets Due to Wrong Bar Code

    C. O. Truxton is recalling 287 bottles of Doxycycline Hyclate Tablets, 100 mg, because the product bears the wrong bar code.

    Product
    Doxycycline Hyclate Tablets, USP, 100 mg, 500-count bottle, Rx only, Distributed by: Truxton Inc. Bellmawr, NJ 08031, Manufactured for: Blu Caribe Dorado, PR 00646 USA, NDC 0463-6000-50 (top panel) NDC 24658-312-05 (side panel)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0268-2016·2015-11-18

    Medtronic Perfusion Tubing Packs Recalled for Potential Header Bag Seal Breach

    Medtronic is recalling 496 Perfusion Tubing Packs due to a potential breach in the header bag seal. The affected lots were distributed nationwide in the US.

    Product
    Medtronic Perfusion Tubing Packs, Models TL7M64R3, TL7P17R1 & HY2W85R9, Sterilized using Ethylene Oxide. The Tubing Pack design and components are specified by the user, they are packaged with consideration of setup efficiency and respect for the environment, and they are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0239-2016·2015-11-18

    Beckman Coulter Recalls Access CEA Assay Reagent Packs for Filling Errors

    Beckman Coulter is recalling Access CEA Assay reagent packs because they were filled incorrectly. The recall covers 11,406 units distributed worldwide.

    Product
    Access CEA Assay, Part No. 33200. For the quantitative determination of Carcinoembryonic Antigen (CEA) levels in human serum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0270-2016·2015-11-18

    Stryker Spine Recalls Radius Rod to Rod Connectors for Missing Clearance

    Stryker Spine is recalling 42 units of Radius Rod to Rod Connectors because the device lacks the required FDA 510(k) clearance.

    Product
    Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion using autograft or allograft in skeletally mature patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0235-2016·2015-11-18

    Stryker Recalls Reprocessed Surgical Drill Bits Due to Packaging Seal Issues

    Stryker Sustainability Solutions is recalling 1,202 reprocessed surgical drill bits and blades because packaging was not properly sealed.

    Product
    SSS Reprocessed Zimmer, Synthes, Stryker and Linvatec Drill Bits and Blades Surgical drill bits, blades, burs, chisels, rasps, taps and reamers are specially designed surgical accessories to help the surgeon cut and drill bone and bony structures. Reprocessed surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0253-2016·2015-11-18

    CooperSurgical Recalls MILEX Pessary Kits Due to Incorrect Packaging Labels

    CooperSurgical is recalling 144 MILEX Pessary Kits because the outer packaging displays incorrect size prints, although the pessary pouch itself is correctly marked.

    Product
    MILEX PESSARY KIT; Model Numbers: MXPES00; MXKPES00; MXKPREG03; MXKPGSK07 Product Usage: The Coopersurgical MILEX SILICONE PESSARY is used to manage a number of gynecologic issues including pelvic support defects and stress urinary incontinence.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V761000·2015-11-17

    Airstream Recalls 2016 Trailers Due to Propane Gas Leak Risk

    Airstream is recalling 904 model year 2016 recreational trailers because propane gas may leak from the regulator, increasing the risk of a fire.

    Product
    AIRSTREAM — AIRSTREAM INTERNATIONAL, SPORT, CLASSIC, LAND YACHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16038·2015-11-17

    PetSmart Recalls Glass Fish Bowls Due to Laceration Hazard

    PetSmart is recalling Grreat Choice and Top Fin glass fish bowls because they can shatter during normal handling, posing a laceration risk.

    Product
    Glass fish bowls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16035·2015-11-17

    REI Recalls Outdoor Rocker Chairs Due to Fall Hazard

    REI is recalling evrgrn Campfire Rocker Chairs because they can tip backwards while rocking, posing a fall hazard to users.

    Product
    evrgrn Campfire Rocker Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16036·2015-11-17

    PetSmart Recalls Top Fin Betta Bowl Kits Due to Laceration Hazard

    PetSmart is recalling Top Fin Betta Bowl Kits with LED lights because the glass bowls can crack or shatter, posing a laceration hazard.

    Product
    Top Fin Betta Bowl Kit with LED Light
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16037·2015-11-17

    Kona Recalls 2014 Wo Bicycles Due to Fork Breakage Hazard

    Kona is recalling about 530 2014 Wo bicycles because the fork can crack or break, posing a fall hazard. Consumers should stop using the bikes and contact Kona for a free replacement.

    Product
    Kona Wo bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V763000·2015-11-17

    Ford E-Series Wheelchair Lift Recall Due to Platform Cracking

    Mobility Specialists is recalling 2006-2014 Ford E-250 and E-350 vans with Ricon wheelchair lifts. The platform side plates may crack or bearings may shift, causing the lift to fall and injure the operator.

    Product
    FORD — FORD E-250, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·141-2015·2015-11-17

    Tyson Recalls Fully Cooked Hot Wings Due To Off Odor

    Tyson Foods is recalling approximately 52,486 pounds of fully cooked hot wings due to possible adulteration from an off odor.

    Product
    Tyson Foods, Inc. — Tyson Foods Inc. Recalls Chicken Product Due To Possible Adulteration
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V759000·2015-11-16

    Hyundai Recalls 2011-2012 Sonata Vehicles Due to Brake Pedal Defect

    Hyundai is recalling 2011-2012 Sonata vehicles because a deteriorating brake pedal stopper pad may prevent the brake light switch from retracting, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V756000·2015-11-16

    Hyundai Recalls 2013-2015 Genesis Coupe for Differential Bolt Loosening

    Hyundai is recalling 2013-2015 Genesis Coupes with manual transmissions because rear differential bolts may loosen, potentially causing loss of propulsion and increased crash risk.

    Product
    HYUNDAI — HYUNDAI GENESIS COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide