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.

50001–50025 of 73852

  • ModerateFDA (Devices)·Z-0776-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc is recalling specific dental implants because safety information was omitted from the instructions for use.

    Product
    IMPLANT,TM, MTX 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMMB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0577-2016·2016-02-17

    Bulletproof Recalls Tangerine FATwater Bottles Due to Microbial Growth

    Bulletproof Digital Inc is recalling 5,748 bottles of Tangerine FATwater due to microbial growth detection. No pathogens were detected.

    Product
    FATwater bottle, 16.9 fl. oz., Tangerine flavor, UPC 6 41871 93693 9
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0775-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Instructions in Manual

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because critical safety information was missing from the instruction manual.

    Product
    IMPLANT,TM, MTX 3.7 mm x 10 mm diameter 3.5 mm Catalog #TMMB10 Product Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or more…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0758-2016·2016-02-17

    Spectranetics Recalls Expired 2.3mm Turbo-Power Laser Atherectomy Catheters

    Spectranetics Corp. is recalling 8 units of 2.3mm Turbo-Power OTW Manual laser atherectomy catheters because they are past their expiration date.

    Product
    2.3mm Turbo-Power OTW, Manual, Model No 423-050 Product Usage The Turbo-Power System (Laser Atherectomy Catheter) is a laser atherectomy device designed for use with the CVX-300" Excimer Laser System. The Turbo-Power Laser Atherectomy Catheter is a sterile, single use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0779-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific Trabecular Metal dental implants because safety information was omitted from the latest instructions for use.

    Product
    IMPLANT,TM, MTX FULL 4.1 mm x 11.5 mm diameter 3.5 mm Catalog #TMT4B11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0654-2016·2016-02-17

    Fagron Recalls SyrSpend SF Syrup Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF syrup-suspending vehicle due to the presence of yeast. The recall affects 44 bottles distributed nationwide.

    Product
    SyrSpend SF, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 500 mL bottle, Manufactured by Fagron Inc., St. Paul, MN 55120, NDC 51552-1079-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0784-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc. is recalling specific dental implants because safety information was missing from the instructions for use.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 16 mm diameter 3.5 mm Catalog #TMTB16 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0660-2016·2016-02-17

    Amerisource Recalls Candesartan Cilexetil Tablets Due to Impurity Failures

    Amerisource Health Services is recalling 716 cartons of Candesartan Cilexetil Tablets, 16 mg, due to failed impurities and degradation specifications.

    Product
    Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0782-2016·2016-02-17

    Zimmer Dental Implants Recalled for Missing Instructions in Manual

    Zimmer Dental Inc is recalling specific Trabecular Metal implants because the latest instruction manual omitted critical safety information for certain sizes.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMTB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0777-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Instructions

    Zimmer Dental Inc. is recalling specific dental implants because important safety information was missing from the latest instruction manual.

    Product
    IMPLANT,TM, MTX 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMMB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V086000·2016-02-16

    Starcraft AR-One Toy Hauler Recall for Incorrect Tire Labels

    Starcraft is recalling 2016 AR-One toy hauler trailers because incorrect tire labels may lead to improper tire replacement, increasing crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V087000·2016-02-16

    Mercedes-Benz Recalls 2016 C300 and C450 Models for Sunroof Defect

    Mercedes-Benz is recalling specific 2016 C300 and C450 vehicles because the panoramic sunroof glass may not be properly bonded and could detach during operation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C300, C450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V088000·2016-02-16

    IMT Recalls Dominator Cranes Due to Valve Bank Cover Defect

    Iowa Mold Tooling is recalling 2013-2016 Dominator vehicles because a valve bank cover may crack and fall off, creating a road hazard.

    Product
    IMT — IMT DOMINATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V085000·2016-02-12

    Trans Tech Student Safety Transporter School Bus Barrier Recall

    Transportation Collaborative is recalling 2012-2015 Trans Tech Student Safety Transporter school buses because the driver's side barrier may not deform properly in a crash.

    Product
    TRANS TECH BUS — TRANS TECH BUS STUDENT SAFETY TRANSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16101·2016-02-12

    Crescent Point Energy Recalls Propane Gas Due to Fire and Burn Hazards

    Crescent Point Energy is recalling approximately 118 million gallons of propane gas in the U.S. because insufficient odorant levels may prevent consumers from detecting leaks, posing fire and burn risks.

    Product
    Propane (LP) Gas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V081000·2016-02-11

    Mercedes-Benz and Chrysler Recall Vehicles Due to Air Bag Inflator Defect

    Mercedes-Benz and Chrysler are recalling specific vehicles because the driver's frontal air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ, CHRYSLER E63, ML63, GL350, GL450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V083000·2016-02-11

    Volkswagen Recalls 2009 Routan Vehicles Due to Air Bag Control Unit Defect

    Volkswagen is recalling 2009 Routan vehicles because the air bag control unit may corrode and fail, potentially preventing air bag deployment or causing unintended deployment.

    Product
    VOLKSWAGEN — VOLKSWAGEN ROUTAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V084000·2016-02-11

    GM Recalls 2016 Vehicles for Missing Audio Safety Warnings

    General Motors is recalling 2016 Chevrolet and GMC vehicles because the radio may fail to provide audio warnings for unbelted drivers or keys left in the ignition.

    Product
    GMC — GMC, CHEVROLET SIERRA, SILVERADO, MALIBU, CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V082000·2016-02-11

    Starcraft RV Recalls 2016 Trailers Due to Water Heater Overheating Risk

    Starcraft RV is recalling 2016 Solstice and Travel Star trailers because water heaters may overheat, posing a scalding risk.

    Product
    STARCRAFT RV FW — STARCRAFT RV FW, STARCRAFT RV TT SOLSTICE, TRAVEL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V078000·2016-02-10

    Volkswagen and Audi Vehicles Recalled for Air Bag Inflator Rupture Risk

    Volkswagen Group of America is recalling specific 2007-2014 Volkswagen and Audi models because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI EOS, CC, Q5, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0691-2016·2016-02-10

    Draeger Oxylog 2000 Plus Ventilator Recalled for Malfunction

    Draeger Medical is recalling Oxylog 2000 Plus ventilators because a software error can stop ventilation and trigger alarms.

    Product
    Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and transport ventilator with pressure support.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V079000·2016-02-10

    Volkswagen Recalls Audi and Passat Vehicles for Airbag Inflator Defect

    Volkswagen is recalling 151,767 Audi and Volkswagen vehicles because the driver's airbag inflator may rupture during deployment, potentially causing serious injury.

    Product
    AUDI — AUDI, VOLKSWAGEN A3, A4 CABRIOLET, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0692-2016·2016-02-10

    Draeger Oxylog 3000 Ventilators Recalled for Software Error

    Draeger Medical is recalling Oxylog 3000 and Oxylog 3000 Plus ventilators because a software error can stop ventilation and trigger alarms.

    Product
    Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus Ventilator Catalog Numbers: 2M86300/2M86965 and 5704813/5704831. Volume controlled and pressure-controlled emergency and transport ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V077000·2016-02-10

    Daimler Vans Recalls Sprinter Vehicles Due to Air Bag Inflator Rupture Risk

    Daimler Vans is recalling 2007-2014 Dodge, Freightliner, and Mercedes-Benz Sprinter vans because the driver's air bag inflator may rupture during deployment.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ, DODGE SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide