The Recall Desk

State

American Samoa product recalls

72,907 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
5
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 5 (20%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1226–1250 of 72932

  • ModerateFDA (Devices)·Z-2422-2026·2026-06-24

    Medline abdominal and bariatric packs contain recalled Mastisol liquid adhesive

    Medline convenience kits including abdominal, bariatric and laparoscopic cholecystectomy packs are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRIC + DYNJ904119O BARIATRIC CDS CDS983883J BWNBORO LAP CHOLE PACK-LF DYNJ32836B CCSB KARIN JWIRE LUMPECTOMY DYNJ910459B CHRISTUS CHILDRENS LAP CHOLE DYNJ61165G CUH MINOR PACK-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2424-2026·2026-06-24

    Medline basic and laparoscopy packs contain recalled Mastisol liquid adhesive

    Medline convenience kits including basic packs, general laparoscopy, CVC insertion bundles and da Vinci packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA DYNJ58305 CHRISTUS CH PEDIATRIC BASIC DYNJ61167G CVC INSERTION BUNDLE CVI3940A DAVINCI PACK SURGICOUNT DYNJ45544F EPCH BASIC PACK DYNJ83094C GENERAL PACK D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0604-2026·2026-06-24

    Dental City benzocaine anesthetic gel bottles may have incomplete seals

    Dental City Topical Anesthetic Gel, benzocaine 20% strawberry flavor, is being recalled because the product may contain bottles with incomplete seals. 450 units are affected.

    Product
    DENTAL CITY TOPICAL ANESTHETIC — DENTAL CITY TOPICAL ANESTHETIC (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0633-2026·2026-06-24

    Rapidol triple antibiotic first aid ointment recalled over manufacturing deviations

    Rapidol Triple Antibiotic First Aid Ointment, 2 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 84 tubes are affected.

    Product
    Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, Polymyxin-B Sulfate 5,000 units, net wt. 2oz (57g) tubes, Distributed by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 10096 77162 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2425-2026·2026-06-24

    Medline IV start kits with HubGuard contain recalled Mastisol adhesive

    The Medline IV Start Kit with HubGuard is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

    Product
    Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0631-2026·2026-06-24

    Circle K triple antibiotic ointment recalled over manufacturing practice deviations

    Circle K Triple Antibiotic Ointment, 0.5 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 2,420 tubes are affected.

    Product
    Circle K, triple antibiotic ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000 units), net wt. 0.5 oz (14.2g) tubes, Product manufactured for Lil' Drug Store Products, Inc., 9300 Earhart Lane SW, Cedar Rapids, IA 52404, Made in India, UPC
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2436-2026·2026-06-24

    Medline ACDF and ACL procedure kits contain recalled Mastisol adhesive

    Medline convenience kits for ACD, ACDF, ACL and ALIF procedures are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911996 ACL ACCESSORY PACK DYNJ86584B ACL- LF DYNJ905281B ACL PACK DYNJ67271A ALIF DYNJ904848L ANTERIOR CERVICAL DYNJ901355J ARTHROSCOPY DYN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2419-2026·2026-06-24

    Medline central line dressing and port kits contain recalled Mastisol

    Medline central line dressing kits, PICC/CVC/midline CHG dressing kits, port-a-cath kits and vein ablation packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2426-2026·2026-06-24

    Medline pediatric dressing change kits contain recalled Mastisol liquid adhesive

    The Medline Kit: Dressing Change Ped is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

    Product
    Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2431-2026·2026-06-24

    Medline da Vinci and gynaecology laparoscopy kits contain recalled Mastisol

    Medline da Vinci, general robotics and gynaecology laparoscopy convenience kits are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.

    Product
    Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS982371I GYN LAPAROSCOPY CDS #34-RF CDS920099S GYN LAPAROSCOPY PACK DYNJT3887
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2449-2026·2026-06-24

    HarmonyAIR A-Series surgical light intensity control buttons may detach

    HarmonyAIR A-Series Surgical Lighting Systems are being recalled because the plus and minus buttons used to control light intensity on the light heads may detach. 2,101 units affected.

    Product
    HarmonyAIR A-Series Surgical Lighting System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2437-2026·2026-06-24

    Centurion dialysis and dressing change kits contain recalled Mastisol adhesive

    Centurion convenience kits including dialysis catheter maintenance and dressing change trays are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.

    Product
    Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS CATHETER MAINTENANCE KIT DT17570 DIALYSIS DRESSING CHANGE KIT DT21370B DRESSING CHANGE TRAY - GOLD DT21115B PORT DRESSING CHANGE KIT DYNDC2815A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2448-2026·2026-06-24

    HarmonyAIR A-Series surgical light heads may show paint delamination

    HarmonyAIR A-Series Surgical Lighting Systems are being recalled because of the potential for paint delamination, meaning chipping or peeling, on the light heads. 4,138 units affected.

    Product
    HarmonyAIR A-Series Surgical Lighting System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2442-2026·2026-06-24

    Medline femoral block trays contain recalled Mastisol liquid adhesive

    The Medline Femoral Block Tray is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

    Product
    Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2432-2026·2026-06-24

    Medline C-section kits contain recalled Mastisol adhesive with cracking tubing

    Medline C-Section Kits and Packs are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

    Product
    Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0630-2026·2026-06-24

    Lucky Super Soft triple antibiotic ointment recalled over manufacturing deviations

    Lucky Super Soft First Aid Triple Antibiotic Ointment, 0.5 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 2,503 tubes are affected.

    Product
    Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 units, neomycin sulphate 3.5 mg, polymyxin B sulphate 5000 units, Net Wt. 0.5 oz (14g) tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0636-2026·2026-06-24

    Med Pride bacitracin zinc ointment 500 units recalled over manufacturing deviations

    Med Pride Bacitracin Zinc Ointment, 500 units per gram in 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,374 tubes affected.

    Product
    Med Pride, Bacitracin Zinc Ointment, 500 units, 1oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30354 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0640-2026·2026-06-24

    Med Pride hydrocortisone cream 1oz tubes recalled over manufacturing deviations

    Med Pride Hydrocortisone Cream 1%, 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,944 tubes are affected.

    Product
    Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 1 oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30503 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2433-2026·2026-06-24

    Medline LAVH packs contain recalled Mastisol liquid adhesive

    The Medline WT LAVH Pack is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.

    Product
    Medline convenience kits: WT LAVH PACK DYNJ46609F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0602-2026·2026-06-24

    DHP benzocaine topical anesthetic gel bottles may have incomplete seals

    DHP Topical Anesthetic Gel, benzocaine 20% strawberry flavor, is being recalled because the product may contain bottles with incomplete seals. 150 units are affected.

    Product
    HEALTH-TEC TOPICAL ANESTHETIC — HEALTH-TEC TOPICAL ANESTHETIC (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0608-2026·2026-06-24

    Focalin XR 5mg capsules carry incorrect or missing lot and expiry

    Focalin XR 5 mg extended-release capsules are being recalled over a labeling issue: incorrect or missing lot number and/or expiry date. 7,803 bottles are affected.

    Product
    FOCALIN — FOCALIN (DEXMETHYLPHENIDATE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V399000·2026-06-23

    GM Recalls 2025-2026 Savana and Express for Steering Nut Issue

    General Motors is recalling 2025-2026 GMC Savana and Chevrolet Express vehicles because a steering gear nut may be loose, risking loss of control.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V400000·2026-06-23

    Hyundai Tucson instrument panel displays may fail due to software error

    Hyundai is recalling certain 2025-2026 Tucson, Tucson Hybrid and Tucson Plug-In Hybrid vehicles because a software error may cause the instrument panel display to fail.

    Product
    HYUNDAI — HYUNDAI TUCSON PLUG-IN HYBRID, TUCSON HYBRID, TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E037000·2026-06-23

    Rockford Fosgate Amplifier Kits Recalled for Fire Risk

    Rockford Corporation is recalling specific amplifier kits because a fuse may fail to protect against short circuits, increasing the risk of a fire.

    Product
    ELECTRICAL SYSTEM:WIRING:FUSES AND CIRCUIT BREAKERS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide