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.

21276–21300 of 73413

  • ModerateFDA (Drugs)·D-0685-2022·2022-03-30

    Fluocinonide Topical Solution Recalled Due to Manufacturing Deviations

    Teligent Pharma recalled Fluocinonide Topical Solution USP 0.05% nationwide because the manufacturer is discontinuing stability testing. Without ongoing verification, the company cannot ensure product safety.

    Product
    Fluocinonide Topical Solution USP, 0.05%, packaged in a) 20 mL bottles, NDC 52565-025-20; b) 60 mL bottles, NDC 52565-025-59, Rx only, Teligent Pharma, Inc., Buena, New Jersey 08310.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0700-2022·2022-03-30

    Clobetasol Propionate Cream USP Recalled for cGMP Deviations

    Teligent Pharma, Inc. is recalling Clobetasol Propionate Cream USP 0.05% in 60-gram tubes due to current Good Manufacturing Practice (cGMP) deviations. The firm discontinued its stability study program, affecting all products within expiry nationwide and in Puerto Rico.

    Product
    Clobetasol Propionate Cream USP, 0.05%, packaged in 60 grams tube, Rx only, Manufactured for SOLA Pharmaceuticals, Baton Rouge, LA 70809; NDC 70512-028-60.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0708-2022·2022-03-30

    Norepinephrine Bitartrate Injection Recalled for Defective Container

    Athenex Pharma Solutions is recalling Norepinephrine Bitartrate Injection 8 mg per 250 mL due to a defective container. The recall affects approximately 9,800 bags distributed nationwide.

    Product
    Norepinephrine Bitartrate Injection 8 mg per 250 mL in 0.9% Sodium Chloride, 8 mg, 250 mL excel bag, Rx only, Athenex Pharma Solutions, LLC, Clarence, NY, 14031, NDC 76154-475-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0720-2022·2022-03-30

    Compounded injectable Formula F9 recalled for insufficient potency

    Olympia Compounding Pharmacy recalled Formula F9, a compounded injectable medication, because the product was sub-potent with insufficient active ingredient. The recall affected 493 vials distributed nationwide.

    Product
    Formula F9, Papaverine 0.9 mg/mL, Phentolamine 0.1 mg/mL, PGE 20 mcg/mL, Atropine 0.01 mg/mL, Multi-Dose 10 mL vial, Each ML contains: 0.5% Chlorobutanol NF, 0.005% Edetate Disodium Dihydrate USP, 2.74% Benzyl Alcohol NF, 5% Mannitol USP, 1% Sodium Metabisulfite NF, 1% Ethyl…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0699-2022·2022-03-30

    Triamcinolone Acetonide Ointment Recalled Due to cGMP Deviations

    Teligent Pharma is recalling Triamcinolone Acetonide Ointment USP 0.1% nationwide because the manufacturer is discontinuing its stability study program, creating a current Good Manufacturing Practice (cGMP) deviation.

    Product
    Triamcinolone Acetonide Ointment USP, 0.1%, packaged in a) 15 grams tubes, NDC 52565-014-15; b) 80 grams tubes, NDC 52565-014-80; c) 1 lb (454 g) jars, NDC 52565-014-26; Rx only, Teligent Pharma, Inc., Buena, New Jersey 08310.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0714-2022·2022-03-30

    Diclofenac Sodium Topical Solution recalled due to leaking containers

    Direct Rx is recalling Diclofenac Sodium Topical Solution 1.5% (150 mL) nationwide due to defective containers that may leak. Consumers who have purchased this product should stop use and contact their pharmacy or physician.

    Product
    Diclofenac Sodium Topical Solution 1.5%, 150 mL, Rx only, Packaged and Distributed by: Direct Rx Dawsonville, GA 30534 Mfg. For SOLA Pharmaceuticals Baton Rouge, LA, NDC 61919-675-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0718-2022·2022-03-30

    Sermorelin Acetate Injectable Recalled for Sub-Potent Strength

    Olympia Compounding Pharmacy is recalling Sermorelin Acetate 9 mg multi-dose vials nationwide due to sub-potency. The affected lots do not contain the full intended strength of the medication.

    Product
    Sermorelin Acetate Lyophilized powder for reconstitution, Multi-Dose 9 mg per vial, Each ML contains: 5% Mannitol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0059-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0679-2022·2022-03-30

    Diclofenac Sodium Topical Solution recalled by Teligent Pharma

    Teligent Pharma is recalling all unexpired batches of Diclofenac Sodium Topical Solution 1.5% due to current good manufacturing practice (cGMP) deviations related to discontinuation of the firm's stability study program.

    Product
    Diclofenac Sodium Topical Solution USP, 1.5% w/w, 5 fl. oz. (150 mL) bottle, Rx only, Teligent Pharma, Inc., Buena, New Jersey 08310, NDC 52565-002-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0688-2022·2022-03-30

    Halobetasol Propionate Ointment Recalled for cGMP Deviations

    Teligent Pharma is recalling all unexpired batches of Halobetasol Propionate Ointment 0.05% nationwide due to cGMP deviations. The manufacturer is discontinuing its stability study program.

    Product
    Halobetasol Propionate Ointment, 0.05%, Net Wt. 50 grams tube, Rx only, Manufactured for: SOLA Pharmaceuticals, Baton Rouge, LA 70809, NDC 70512-033-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0670-2022·2022-03-30

    Clobetasol Propionate Cream Recalled Due to cGMP Deviations

    Teligent Pharma is recalling all unexpired batches of Clobetasol Propionate Cream USP 0.05% nationwide because the manufacturer is discontinuing its stability study program and cannot ensure compliance with current Good Manufacturing Practice standards.

    Product
    Clobetasol Propionate Cream USP, 0.05%, packaged in a) 15 grams tube, NDC 52565-051-15; b) 30 grams tube, NDC 52565-051-30; c) 45 grams tube, NDC 52565-051-45; d) 60 grams tube, NDC 52565-051-60; Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0691-2022·2022-03-30

    Halobetasol Propionate Ointment recalled due to cGMP deviations

    Teligent Pharma is recalling all unexpired Halobetasol Propionate Ointment 0.05% (21,323 tubes) due to current good manufacturing practice (cGMP) deviations. The firm is discontinuing its stability study program.

    Product
    Halobetasol Propionate Ointment, 0.05%, Net Wt. 50 grams 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 63739-998-67.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0705-2022·2022-03-30

    Lidocaine Ointment USP 5% Recalled Due to cGMP Deviations

    Teligent Pharma, Inc. is recalling Lidocaine Ointment USP 5% nationwide because the manufacturer is discontinuing its stability study program, which constitutes a deviation from current good manufacturing practice (cGMP). All products within their expiration dates are affected.

    Product
    Lidocaine Ointment USP, 5%, Net Wt 35.44 g (1 1/4 Oz) tube, Rx Only, Manufactured for: Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701, NDC 50383-341-35.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0723-2022·2022-03-30

    Hydroxocobalamin B12 Injection Recalled for Sub-Potent Dose

    Olympia Compounding Pharmacy is recalling Hydroxocobalamin B12 1mg/mL injection vials distributed nationwide because the product is sub-potent (below specified strength). The firm initiated this voluntary recall on March 8, 2022.

    Product
    Hydroxocobalamin B12 1mg/mL, Multi-Dose 30 mL vial, Each ML contains: 0.82% Sodium Chloride USP, 0.9% Benzyl Alcohol NF, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals Conroy Rd., Ste. 155, Orlando, FL 32835 NDC 73198-0080-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E027000·2022-03-29

    Meritor 180 Series Drive Pinions Recalled for Fracture Risk

    Meritor is recalling 180 Series Drive Pinions because they may fracture. A fractured pinion could engage the parking brake without warning, increasing crash risk.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V202000·2022-03-29

    2022 Kia Sorento Oil Supply Pipe May Crack, Creating Fire Risk

    Kia is recalling certain 2022 Sorento vehicles because the turbocharger oil supply pipe may crack, causing an oil leak that could increase the risk of engine fire.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V203000·2022-03-29

    Travel trailers with defective power inlet bolts risk fire

    Grand Design is recalling certain 2022 Reflection and Transcend travel trailers with 50-amp shore power inlets. The power inlet lug bolts may be too hard to tighten properly, creating loose electrical connections that can cause fire.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION, TRANSCEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V198000·2022-03-28

    Bugatti Recalls One 2018 Chiron for Loose Front Frame Support Screw

    Bugatti is recalling one 2018 Chiron vehicle because a screw fastening the front frame support may be loose, potentially reducing structural protection in a crash.

    Product
    BUGATTI — BUGATTI CHIRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V195000·2022-03-28

    2022 Keystone Travel Trailers Recalled for Improper Hitch Welds

    Keystone is recalling certain 2022 Bullet, Outback, and Passport travel trailers due to improper welds on the coupler hitch. The defect can cause the trailer to separate from the tow vehicle, increasing crash and injury risk.

    Product
    KEYSTONE — KEYSTONE PASSPORT, OUTBACK, BULLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V194000·2022-03-28

    Mercedes-Benz Recalls 2022 S-Class Vehicles for Rear Axle Weld Defect

    Mercedes-Benz is recalling 2022 S 500 and S 580 vehicles because a rear axle weld may be defective, posing a risk of loss of vehicle control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 500 4MATIC, S 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V152000·2022-03-28

    Certain Volkswagen Atlas vehicles recalled for airbag deployment delay

    Volkswagen is recalling certain Atlas and Atlas Cross Sport vehicles because corroded electrical contacts in the front door wiring harness may delay airbag deployment during side impacts, increasing the risk of injury.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V201000·2022-03-28

    Lance Recalls 2022 Travel Trailers Due to Fire Risk from Data Cable

    Lance is recalling 2022 travel trailers because a data cable may rest on a burner box, increasing the risk of a fire. Dealers will reroute the cable free of charge.

    Product
    LANCE — LANCE 2185, 1995, 1685, 1985
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V200000·2022-03-28

    Lance Truck Campers Recalled for Data Cable Fire Risk

    Lance Camper is recalling 2022 models because a data cable may rest on the burner box, increasing the risk of a fire.

    Product
    LANCE — LANCE 825, 650, 1172, 865
    Category
    Vehicle
    Distribution
    Distributed nationwide