State

American Samoa product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52801–52825 of 73858

ModerateFDA (Devices)·Z-2155-2015·2015-07-29
Cochlear Nucleus Sterile Silicone Template Recalled for Expiration
Cochlear Americas is recalling 26 units of Nucleus Sterile Silicone Templates because expired product was distributed to specific US states.
Product
Cochlear Nucleus Sterile Silicone Template Product Usage: The Cochlear Nucleus Sterile Silicone Template is used in the sterile field to check the size of the periosteal pocket, the shape and depth of the implant well and appropriate positions for tie down holes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1256-2015·2015-07-29
Wockhardt Recalls Amlodipine Besylate Tablets Due to CGMP Deviations
Wockhardt USA is recalling Amlodipine Besylate 10 mg tablets because the firm did not adequately investigate customer complaints.
Product
Amlodipine Besylate Tablets, 10 mg Tablets, Packaged as A) 90 Count Bottles (NDC: 64679-423-01) and B) 1000 Count Bottles (NDC: 64679-423-02, Rx Only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2180-2015·2015-07-29
FDA Recalls Fiber Stripper Tools Due to Cleaning Validation Issues
American Medical Systems is recalling 16,710 Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Tool, Stripper W/BLD, 44S, Nonautoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1270-2015·2015-07-29
Wockhardt Recalls Metoprolol Succinate Extended-Release Tablets Due to CGMP Deviations
Wockhardt USA Inc. is recalling Metoprolol Succinate Extended-Release Tablets, 100 mg, because the firm did not adequately investigate customer complaints.
Product
Metoprolol Succinate Extended-Release Tablets, USP, 100 mg Tablets, Packaged in A) 100 Count Bottles (NDC: 64679-0736-02), B) 500 Count Bottles (NDC: 64679-0736-03), and C) 12 x 30 Tablet Dispenser Pack Cartons (NDC: 64679-0736-09), Rx Only. Manufactured by: Wockhardt Limited…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2158-2015·2015-07-29
FDA Recalls Sureflex 273 Lithotripsy Fibers Due to Cleaning Validation Issues
American Medical Systems is recalling Sureflex 273 Lithotripsy Fibers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Sureflex 273 Lithotripsy Fiber, 5x, Blue; Sure F!ex laser fibers are intended for use in laser-based surgical applications, including, but not limited to endoscopic, laparoscopic and open surgical procedures involving vaporization, ablation, coagulation, hemostasis, excision…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1249-2015·2015-07-29
Wockhardt Recalls Clarithromycin Tablets Due to Complaint Investigation Failures
Wockhardt USA is recalling 59,729 bottles of Clarithromycin 500 mg tablets because the firm did not adequately investigate customer complaints.
Product
Clarithromycin Tablets, USP, 500 mg Tablets, 60 Count Bottles, Rx Only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA. NDC: 64679-949-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1261-2015·2015-07-29
Wockhardt Recalls Lisinopril Tablets Due to Complaint Investigation Failures
Wockhardt USA is recalling Lisinopril 40 mg tablets because the firm did not adequately investigate customer complaints.
Product
Lisinopril Tablets USP, 40 mg Tablets, Packaged in A) 100 Count Bottles (NDC: 64679-942-01), B) 500 Count Bottles (NDC: 64679-942-05), and C) 1000 Count Bottles (NDC: 64679-942-02), Rx Only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2164-2015·2015-07-29
FDA Recalls Fiber Stripper Tools Due to Sterilization Validation Issues
American Medical Systems is recalling Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Fiber Stripper, 150¿m, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes, corresponding…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2130-2015·2015-07-29
Perkin Elmer WIZARD2 Gamma Counter Recalled for Barcode Label Error
Perkinelmer is recalling 179 WIZARD2 gamma counters because a barcode label error may produce erroneous results.
Product
Perkin Elmer WIZARD2 1-detector,3", 1000 samples Product Code: 2480-0010 The Wizard¿" gamma counter is intended to detect and count gamma radiation emitted by clinical samples.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2159-2015·2015-07-29
FDA Recalls Sureflex 365 Lithotripsy Fibers Due to Sterilization Validation Issues
American Medical Systems is recalling 16,710 Sureflex 365 Lithotripsy Fibers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Sureflex 365 Lithotripsy Fiber, 5x, Blue; Sure F!ex laser fibers are intended for use in laser-based surgical applications, including, but not limited to endoscopic, laparoscopic and open surgical procedures involving vaporization, ablation, coagulation, hemostasis, excision…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1251-2015·2015-07-29
Wockhardt Recalls 15 mg Lansoprazole Capsules Due to Complaint Investigation Failures
Wockhardt USA is recalling 848 pouches of 15 mg Lansoprazole Delayed-Release Capsules because the firm did not adequately investigate customer complaints.
Product
Lansoprazole Delayed-Release Capsules, USP, 15 mg Capsules, For Repackaging Only, Packaged in 4500 Count Pouches, Over the Counter. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA. NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2185-2015·2015-07-29
FDA Recalls Disposable Fiber Strippers Due to Sterilization Validation Issues
American Medical Systems is recalling 16,710 disposable fiber strippers because cleaning and sterilization validation data do not meet FDA guidance for reusable products.
Product
Stripper, 0.4mm Disposable EndoStat Fiber, The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1277-2015·2015-07-29
Wockhardt Recalls Captopril Tablets Due to Complaint Investigation Failures
Wockhardt USA is recalling 68,969 bottles of Captopril 100 mg tablets because the firm did not adequately investigate customer complaints.
Product
Captopril Tablets, USP, 100 mg Tablets, Packaged in 100 Count Bottles, Rx only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA. NDC: 64679-0905-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2125-2015·2015-07-29
Perkinelmer WIZARD2 Gamma Counter Recalled for Barcode Label Error
Perkinelmer is recalling 53 WIZARD2 gamma counters because a barcode label error may produce erroneous results.
Product
WIZARD2 2-detector, 550 samples Product Code: 2470-0020 The Wizard¿" gamma counter is intended to detect and count gamma radiation emitted by clinical samples.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2186-2015·2015-07-29
FDA Recalls American Medical Systems Fiber Strippers for Validation Issues
American Medical Systems is recalling 16,710 disposable fiber strippers because cleaning and sterilization validation data do not meet new FDA guidance for reusable products.
Product
Stripper, 0.3mm Disposable EndoStat Fiber, The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1275-2015·2015-07-29
Wockhardt Recalls Captopril Tablets Due to CGMP Deviations
Wockhardt USA is recalling Captopril Tablets, USP, 25 mg due to inadequate investigation of customer complaints.
Product
Captopril Tablets, USP, 25 mg Tablets, Packaged in A) 100 Count Bottles (NDC: 64679-0903-01) and B) 1000 Count Bottles (NDC: 64679-0903-02), Rx only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2201-2015·2015-07-29
Myoscience iovera Smart Tip Recalled for Incorrect Expiration Date Labeling
Myoscience Inc. is recalling iovera 155 Smart Tips because the expiration dates on the outer boxes and pouches are incorrect.
Product
iovera 155 Smart Tip; Catalog numbers:STT0412-10 and STT0412-5 (10 and 5 count respectively) iovera Smart Tips are individually packaged in Tyvek PET pouches, which are then packaged into 5 or 10 pack boxes and shipper boxes. Product Usage: Cyrogenic Surgical Device…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1278-2015·2015-07-29
Purdue Pharma Recalls Intermezzo Sublingual Tablets for Dissolution Failures
Purdue Pharma is recalling Intermezzo (zolpidem tartrate) sublingual tablets because they failed to meet dissolution specifications.
Product
Intermezzo (zolpidem tartrate), sublingual tablet 3.5 mg, 1 tablet per pouch, 30 pouches per carton, Rx only, Distributed by Purdue Pharma L.P. Stamford, CT 06901-3431, NDC 59011-265-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V473000·2015-07-28
Altec Recalls 2006-2015 Aerial Devices Due to Outrigger Interlock Defect
Altec Industries is recalling 2,514 aerial devices from 2006-2015 because the outrigger interlock system may fail to detect proper deployment, risking boom instability and injury.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V477000·2015-07-28
Newmar Recalls Toy Haulers Due to Unprotected Fuel System Fire Risk
Newmar is recalling specific All Star and Canyon Star toy haulers because unprotected plastic wrap around the fuel system could burn if exposed to an ignition source.
Product
NEWMAR — NEWMAR ALL STAR, CANYON STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V471000·2015-07-28
Spartan K2 and K3 Trucks Recalled for Air Suspension Power Loss
Spartan Motors is recalling 2015-2016 K2 and K3 trucks because the air suspension system may lose power, increasing crash risk.
Product
SPARTAN — SPARTAN K2, K3
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V470000·2015-07-28
Chrysler Recalls 2015 Chrysler 200 Vehicles for Electrical Connector Defect
Chrysler is recalling 77,971 model year 2015 Chrysler 200 vehicles because a defective electrical connector may cause intermittent power failures, potentially leading to the vehicle stalling without warning.
Product
CHRYSLER — CHRYSLER 200
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V472000·2015-07-28
Honda Recalls 2016 HR-V Vehicles for Missing Tire Placard
Honda is recalling 11,511 model year 2016 HR-V vehicles because they may be missing the required tire and loading information placard.
Product
HONDA — HONDA HR-V
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15744·2015-07-28
Arctic Cat Recalls Prowler 500 HDX Utility Vehicles Due to Fuel Leak
Arctic Cat is recalling about 2,700 Prowler 500 HDX utility vehicles because fuel can leak from the throttle body, posing a fire hazard.
Product
Arctic Cat Prowler 500 HDX
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·15199·2015-07-28
Diamond Sports Recalls Umpire and Catcher Face Masks Due to Impact Injury Hazard
Diamond Sports is recalling about 10,000 umpire and catcher face masks because harness stitching can fail, posing a risk of impact injury.
Product
Diamond Sports face masks
Category
Consumer Product
Distribution
Distributed nationwide