The Recall Desk

State

American Samoa product recalls

73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21701–21725 of 73413

  • ModerateFDA (Drugs)·D-0565-2022·2022-02-23

    Alprazolam Tablets 0.5 mg Recalled Due to cGMP Deviations

    ANI Pharmaceuticals is voluntarily recalling Alprazolam Tablets USP 0.5 mg in multiple package sizes nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 205,662 bottles distributed across the United States.

    Product
    Alprazolam Tablets, USP 0.5 mg, packaged in a) 100-count bottles (NDC 67253-901-10), b) 500-count bottles (NDC 67253-901-50), and c) 1000-count bottles (NDC 67253-901-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0560-2022·2022-02-23

    Moxifloxacin Ophthalmic Solution Recall for Failed Impurities Specifications

    Aurobindo Pharma USA Inc. is recalling Moxifloxacin Ophthalmic Solution 0.5% due to failed impurities and degradation specifications. The recall affects 115,776 bottles distributed nationwide.

    Product
    MOXIFLOXACIN — MOXIFLOXACIN (MOXIFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0568-2022·2022-02-23

    Pyrazinamide Tablets 500 mg Recalled Due to cGMP Deviations

    ANI Pharmaceuticals, Inc. has recalled Pyrazinamide Tablets USP 500 mg due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 5,477 bottles distributed nationwide.

    Product
    Pyrazinamide Tablets, USP 500 mg, 100-count bottles, Rx only, Manufactured by: ULTRAtab Laboratories, Inc. Highland, NY 12528, Distributed by Par Pharmaceuticals, Chestnut Ridge, NY 10977, NDC 67253-660-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0566-2022·2022-02-23

    Alprazolam Tablets USP 1.0 mg Recalled for cGMP Deviations

    ANI Pharmaceuticals has recalled Alprazolam Tablets USP 1.0 mg distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 173,499 bottles across multiple lot numbers.

    Product
    Alprazolam Tablets, USP 1.0 mg, packaged in a) 100-count bottles (NDC 67253-902-10), b) 500-count bottles (NDC 67253-902-50), and c) 1000-count bottles (NDC 67253-902-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0558-2022·2022-02-23

    Diazepam Oral Solution Recalled for Failed Impurity Specifications

    Lannett Company is recalling Diazepam Oral Solution (Concentrate) 5 mg/mL due to out-of-specification results for related substances, indicating failed impurities and degradation testing.

    Product
    Diazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1768-36.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0643-2022·2022-02-23

    Dental Resins Recalled for Manufacturing Facility and Origin Labeling Violations

    Envisiontec US LLC recalled 795 units of FLEXCERA SMILE dental resins manufactured between April 2021 and September 2021 because they were produced in a non-FDA-registered facility and falsely labeled as German origin.

    Product
    FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0578-2022·2022-02-23

    Chlorthalidone Tablets Recalled for Foreign Matter Contamination

    Sun Pharmaceutical is recalling Chlorthalidone Tablets USP 25 mg (Lot #P0602, expiration 03/2023) due to stainless steel microscopic wear particles, punch lubricant oil, and silicone particles from the dust cup found in the product.

    Product
    CHLORTHALIDONE — CHLORTHALIDONE (CHLORTHALIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0564-2022·2022-02-23

    Alprazolam Tablets USP 0.25 mg Recalled for cGMP Deviations

    ANI Pharmaceuticals is recalling Alprazolam Tablets USP 0.25 mg nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects multiple lot numbers of 100-count, 500-count, and 1000-count bottles distributed across the United States.

    Product
    Alprazolam Tablets, USP 0.25 mg, packaged in a) 100-count bottles (NDC 67253-900-10), b) 500-count bottles (NDC 67253-900-50), and c) 1000-count bottles (NDC 67253-900-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0567-2022·2022-02-23

    Alprazolam Tablets 2.0 mg Recalled for cGMP Deviations

    ANI Pharmaceuticals is recalling Alprazolam Tablets, USP 2.0 mg nationwide due to current good manufacturing practice (cGMP) deviations. The recall affects approximately 70,788 bottles distributed throughout the United States.

    Product
    Alprazolam Tablets, USP 2.0 mg, packaged in a) 100-count bottles (NDC 67253-903-10), b) 500-count bottles (NDC 67253-903-50), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0716-2022·2022-02-23

    Erythromycin Topical Gel Recalled for Failed Impurity Specifications

    Teligent Pharma is recalling one lot of Erythromycin Topical Gel USP 2% because the product failed to meet specifications for unknown maximum related compounds.

    Product
    Erythromycin Topical Gel USP, 2%, Net Wt 30 g tube, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation, dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-053-66.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0641-2022·2022-02-23

    Microbiology quality control kit recalled for incorrect inner label

    A KWIK-STIK quality control kit has an incorrect inner label. The product contains Campylobacter coli, but the inner label states Haemophilus influenzae.

    Product
    KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V100000·2022-02-22

    2021 Porsche Taycan: Center Seat Belt Buckle May Block Child Seat Anchors

    Porsche is recalling 2020-2021 Taycan vehicles with optional rear center seats. The center seat belt buckle wiring harness may obstruct access to child seat anchors, preventing proper installation.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V101000·2022-02-22

    2022 Freightliner Cascadia brake system failure and parking brake defect

    Daimler Trucks North America is recalling 2022 Freightliner Cascadia trucks for a software and brake hardware defect that may cause loss of braking and parking brake functionality, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·007-2022·2022-02-22

    Frickenschmidt Recalls Teriyaki Beef Sticks Due to Gluten Mislabeling

    Frickenschmidt Foods LLC is recalling ready-to-eat teriyaki beef sticks because they are labeled 'gluten free' but contain wheat. No adverse reactions have been reported.

    Product
    Lockwood Packing CO, LLC — Frickenschmidt Foods LLC Recalls Ready-to-Eat Beef Stick Products Due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V099000·2022-02-22

    Mercedes-Benz Metris Recalled for Rearview Camera Display Freeze

    Daimler Vans USA is recalling 2015-2018 Mercedes-Benz Metris vehicles because a defective memory chip may cause the rearview camera image to freeze, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E011000·2022-02-21

    Joyson Recalls Curtain Air Bag Inflators Due to Component Errors

    Joyson is recalling specific curtain air bag inflators because production interruptions may have caused duplicate or missing components, potentially affecting crash performance.

    Product
    AIR BAGS:SIDE/WINDOW:CURTAIN:INFLATOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V096000·2022-02-18

    Kia Recalls 2014 Soul Vehicles Due to Air Bag Software Defect

    Kia is recalling 2014 Soul vehicles because the front air bags may not deploy in a crash if the control unit loses communication with sensors.

    Product
    KIA — KIA SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V098000·2022-02-18

    Mercedes-Benz Recalls 2020 GLE 350 for Wiring Harness Defect

    Mercedes-Benz is recalling 2020 GLE 350 vehicles because an unsecured wiring harness may disable power steering, headlights, or wipers, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V094000·2022-02-18

    Thor Motor Coach Omni and Magnitude motorhomes recalled for LP gas line fire hazard

    Thor Motor Coach is recalling certain 2020-2021 Omni and Magnitude motorhomes due to incorrectly routed LP gas lines that could damage and cause a gas leak, increasing fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OMNI, redundant MAGNITUDE, redundant OMNI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V097000·2022-02-18

    Lance Recalls 2022 Travel Trailers Due to Propane Hose Fire Risk

    Lance Camper is recalling 2022 1685 and 1985 travel trailers because an improperly secured propane hose may contact leaf springs, causing a gas leak and increasing fire risk.

    Product
    LANCE — LANCE 1985, 1685
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V093000·2022-02-17

    Kia Recalls 2013-2014 Optima Vehicles for Fuel Hose Fire Risk

    Kia is recalling 2013-2014 Optima vehicles previously repaired under recall 20V-100 because a damaged or missing heat-protective tape on the low-pressure fuel hose can cause a fuel leak and increase fire risk.

    Product
    KIA — KIA OPTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V091000·2022-02-17

    2022 Chevrolet Corvette rear driveshaft defect may cause loss of power

    General Motors is recalling 2021-2022 Chevrolet Corvette vehicles whose rear half-shaft assemblies may be missing ball bearings. This can cause sudden loss of drive power, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide