The Recall Desk

State

American Samoa product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25076–25100 of 73534

  • ModerateFDA (Devices)·Z-1511-2021·2021-05-05

    Donjoy Ultrasling Pro Arm Sling Recalled for Failed Rivet

    DJ Orthopedics is recalling Donjoy Ultrasling Pro arm slings because a rivet at the chafe tab may fail. The recall covers units distributed in the US and several international countries.

    Product
    DONJOY REF:11-0447-9-ULTRASLING PRO, UNIVERSAL, Rx ONLY, UDI:(01)00190446673552 - Product Usage: intended for medical purposes to immobilize the arm, by means of a fabric band suspended from around the neck.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1507-2021·2021-05-05

    Datascope Cardiosave Rescue IABP Recalled for Cybersecurity Vulnerabilities

    Datascope Corp. is recalling Cardiosave Rescue IABP units due to cybersecurity vulnerabilities in a TCP/IP software library that may cause loss of communication to hospital systems.

    Product
    Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provides temporary support to the left ventricle via the principle of counterpulsation, Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1489-2021·2021-05-05

    Ortho-Clinical VITROS Black Reference Slides Recalled for Mislabeling

    Ortho-Clinical Diagnostics is recalling VITROS Black Reference Slides incorrectly labeled as White Reference Slides, which may cause analyzer delays.

    Product
    VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the reflectometer correction factor adjustment procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1493-2021·2021-05-05

    Cytocell Recalls Chromosome X Alpha-Satellite Probes Due to Cross-Reactivity

    Cytocell Ltd. is recalling 89 Chromosome X Alpha-Satellite probes because users may observe additional signals at 9q34, contradicting the insert.

    Product
    Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte Specific Reagents. Model: MPA3481
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1497-2021·2021-05-05

    Siemens Recalls ARTIS X-Ray Systems Due to Software Issue

    Siemens is recalling 133 ARTIS X-ray systems due to a potential software issue that may require terminating planned procedures.

    Product
    Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS icono floor- 11327700 ARTIS pheno- 10849000 ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1494-2021·2021-05-05

    Coltene Whaledent Recalls TMS LINK PLUS Self-Threading Dental Pins

    Coltene Whaledent Inc is recalling TMS LINK PLUS Self-Threading Dental Pins because incorrect pins were packaged and distributed. The recall affects 65 packs of 20 pins.

    Product
    Dental pins - TMS LINK PLUS Self-Threading Pins - Product Usage: implanted into the teeth or for lab use for dental restoration purposes. The normal procedure requires a hole to be drilled into the tissue of a tooth with an intraoral drill prior to installation. Model…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0340-2021·2021-05-05

    Teligent Pharma Recalls Betamethasone Dipropionate Ointment Due to Impurity

    Teligent Pharma is recalling Betamethasone Dipropionate Ointment 0.05% due to failed impurity specifications. The product is distributed nationwide in 15-gram tubes.

    Product
    Betamethasone Dipropionate Ointment USP, 0.05% (Augmented), packaged in 15 grams tubes, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 08310, Distributed by: McKesson Corporation dba Sky Packaging 4971 Southbridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-996-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1492-2021·2021-05-05

    Boston Scientific Recalls EXALT Controllers Due to Suboptimal Brightness Settings

    Boston Scientific is recalling three EXALT Controllers because they may have been programmed with suboptimal brightness settings, resulting in darker than desired images.

    Product
    EXALT Controller - Product Usage: intended for use with a Boston Scientific endoscope for endoscopic diagnosis, treatment, and video observation. UPN: M00542430
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1502-2021·2021-05-05

    Medela AXS Universal Aspiration Tubing Recalled for Incorrect Expiration Date

    Medela is recalling AXS Universal Aspiration Tubing because the label displays an incorrect expiration date of 2023-07-24 instead of 2021-07-24.

    Product
    Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal Aspiration Tubing is used with the Dominant Flex Surgical Suction Pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0357-2021·2021-05-05

    Genentech Recalls Evrysdi Oral Solution Due to Defective Bottle Adapters

    Genentech is recalling 2,627 bottles of Evrysdi (risdiplam) for oral solution because some have incorrect press-in-bottle-adapters that do not fit co-packed syringes.

    Product
    Evrysdi (risdiplam) for oral solution, 60 mg/80mL (0.75mg/mL), 80 mL total volume after constitution, Rx only, Distributed by: Genentech, Inc. NDC:50242-175-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0339-2021·2021-05-05

    Teligent Pharma Recalls Betamethasone Dipropionate Ointment Due to Impurity Failures

    Teligent Pharma is recalling 79,416 tubes of Betamethasone Dipropionate Ointment USP, 0.05% (Augmented) because the product failed impurity specifications.

    Product
    Betamethasone Dipropionate Ointment USP, 0.05% (Augmented), packaged in 50 grams tubes, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-019-51
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0338-2021·2021-05-05

    Teligent Pharma Recalls Betamethasone Dipropionate Ointment Due to Impurity Failure

    Teligent Pharma is recalling Betamethasone Dipropionate Ointment 0.05% because it failed impurity specifications for a known degradation product.

    Product
    Betamethasone Dipropionate Ointment USP, 0.05% (Augmented), packaged in 15 grams tubes, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-019-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·017-2021·2021-05-04

    Bellisio Recalls Spaghetti with Meat Sauce for Undeclared Soy Allergen

    Bellisio Foods is recalling approximately 3,927 pounds of Michelina's Spaghetti with Meat Sauce due to misbranding and an undeclared soy allergen.

    Product
    Bellisio Foods, Inc. — Bellisio Foods, Inc. Recalls Beef Pasta Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V309000·2021-05-04

    2020 Alfa Romeo Stelvio Braking System Defect Increases Crash Risk

    Chrysler is recalling the 2020 Alfa Romeo Stelvio due to a defect in the anti-lock braking system. Hard braking can cause the ABS hydraulic control unit rotor shaft to separate, reducing braking performance and increasing crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V315000·2021-05-04

    Ducati Recalls Motorcycles Due to Rear Brake System Air Ingress

    Ducati is recalling specific 2016-2020 models because air may enter the rear brake system, reducing braking effectiveness and increasing crash risk.

    Product
    DUCATI — DUCATI XDIAVEL, MONSTER 1200, MONSTER 797, MONSTER 821
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V313000·2021-05-04

    Blue Bird Recalls 2018-2022 All American Buses for Fuel Leak Risk

    Blue Bird is recalling 2018-2022 All American buses because a fuel rail leak could cause a fire. Owners should contact dealers for free repairs.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V314000·2021-05-04

    Arcimoto Motorcycles Recalled for Defective Seat Belt Retractors

    Arcimoto is recalling certain 2019-2021 motorcycles because the seat belt retractor spool sleeve may crack, preventing the belt from retracting. This increases the risk of injury. Owners should contact Arcimoto for free replacement.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V311000·2021-05-04

    Arcimoto Electric Vehicles Recalled: Inverter Software Error Causes Battery Shutdown Risk

    Arcimoto is recalling 2019-2021 FUV, 2020 Deliverator, 2020-2021 Roadster, and 2021 Rapid Responder vehicles due to a software error that may cause unexpected battery shutdown, increasing crash risk. Owners should contact Arcimoto or NHTSA for remedy details.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V312000·2021-05-04

    Blue Bird Recalls 2018-2022 All American Buses Due to Fuel Leak Risk

    Blue Bird is recalling 2018-2022 All American buses because a fuel rail leak could cause a fire. Owners should contact customer service for updates.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, ALL AMERICAN SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V310000·2021-05-04

    2021 Jeep Cherokee Transmission Oil Cooler Hose May Leak and Cause Fire

    Chrysler is recalling certain 2021 Jeep Cherokee vehicles because the transmission oil cooler hose may have been incorrectly cured, allowing transmission fluid to leak and increasing the risk of fire. Dealers will inspect and replace the hose for free.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V308000·2021-05-03

    2021 Hyundai Santa Fe Fuel Pipe Connection Defect Recall

    Hyundai is recalling 2021 Santa Fe vehicles with 2.5-litre Turbo engines due to improperly tightened fuel pipe connections that may leak fuel and increase fire risk. The affected vehicles have already been repaired at dealerships at no cost to owners.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V307000·2021-05-03

    Arcimoto Electric Motorcycles Recalled for Steering Angle Sensor Failure

    Arcimoto is recalling multiple 2019-2021 motorcycle models due to faulty steering angle sensors that may cause oversteer and increase crash risk. The company will update firmware and replace the idler arm at no cost.

    Product
    ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E038000·2021-04-30

    Mando Recalls ABS Modules Due to Electrical Short Circuit Fire Risk

    Mando America Corporation is recalling specific Anti-lock Brake System (ABS) modules that may malfunction and short circuit, increasing the risk of an engine compartment fire.

    Product
    SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E039000·2021-04-30

    Mando Recalls ABS Modules for Brake Fluid Leak and Fire Risk

    Mando America Corporation is recalling certain Anti-lock Brake System (ABS) modules that may leak brake fluid and cause a short circuit, increasing the risk of an engine compartment fire.

    Product
    SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V304000·2021-04-30

    KTM Recalls 790 Adventure Motorcycles Due to Weak Front Brake Spring

    KTM is recalling 2019-2020 790 Adventure models because a weak front brake spring may reduce braking functionality, increasing the risk of a crash.

    Product
    KTM — KTM 790 ADVENTURE, 790 ADVENTURE R, 790 ADVENTURE R RALLY
    Category
    Vehicle
    Distribution
    Distributed nationwide