State

American Samoa product recalls

73,381 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 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20776–20800 of 73406

HighFDA (Devices)·Z-1034-2022·2022-05-11
Ultrasonic Gastrovideoscope Recalled Due to Reprocessing Incompatibility and Infection Control Risk
Olympus recalls the GF-UC140P-AL5 ultrasonic gastrovideoscope nationwide because it is no longer compatible with the OER-Pro reprocessing system, creating an infection control risk to patients.
Product
Ultrasonic Gastrovideoscope, GF-UC140P-AL5. Intended for endoscopic real-time ultrasound imaging.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1033-2022·2022-05-11
Johnson & Johnson Tray Ring Covers Recalled for Sterility Barrier Breach
Johnson & Johnson Surgical Vision is recalling tray ring covers (Model OM271000) worldwide due to a potential breach in the sterility barrier that could allow contamination.
Product
TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0886-2022·2022-05-11
Azurion Medical Imaging System Software Defect Alters Dose Parameters
A software defect in Philips Azurion imaging systems causes the Patient Type to change unexpectedly during study initiation, altering dose control parameters without operator notification.
Product
Azurion systems with software release R1.x
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0843-2022·2022-05-11
Losartan Potassium and Hydrochlorothiazide tablets recalled for AZIDO impurity
Lupin Pharmaceuticals recalls Losartan Potassium and Hydrochlorothiazide tablets nationwide due to manufacturing deviations that resulted in AZIDO impurity levels above acceptable limits.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0844-2022·2022-05-11
Alprazolam XR Extended-Release Tablets Recalled Due to Dissolution Failure
Viatris Inc. is recalling alprazolam XR 3mg tablets (lot EH8348) distributed nationwide due to failed dissolution testing. Tablets may not dissolve properly, potentially reducing drug effectiveness.
Product
ALPRAZOLAM — ALPRAZOLAM (ALPRAZOLAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1027-2022·2022-05-11
Evans Wedge Disposable Trials Orthopedic Surgical Instruments Recalled for Mixed Parts
restor3d Inc. is recalling Evans Wedge Disposable Trials orthopedic surgical instruments because parts were mixed into other lots during relabeling for extended shelf-life. The recall affects devices distributed nationwide across seven states.
Product
Evans Wedge Disposable Trials, Medium Footprint, 10mm Thickness (6101-20181018). Orthopedic manual surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1028-2022·2022-05-11
Evans Wedge Orthopedic Surgical Instrument Recalled for Parts Mixed During Rework
restor3d Inc. is recalling 9 units of Evans Wedge Disposable Trials orthopedic surgical instruments because parts from different lots were mixed during a manufacturing rework and relabeling process.
Product
Evans Wedge Disposable Trials, Large Footprint, 8mm Thickness (Model: 6101-22200818). Orthopedic manual surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1021-2022·2022-05-11
In Vitro Diagnostic Estradiol Test Recalled for Falsely Elevated Results
Siemens Healthcare Diagnostics is recalling Atellica IM Enhanced Estradiol (eE2) 500T diagnostic kits that produce falsely elevated test results in plasma specimens, which could lead clinicians to misinterpret patient results.
Product
Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995562 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0838-2022·2022-05-11
Losartan Potassium tablets recalled for AZIDO impurity above limits
Lupin Pharmaceuticals recalls Losartan Potassium tablets for CGMP deviations with AZIDO impurity above limits. The recall affects 657,336 bottles distributed nationwide; no illnesses reported.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V323000·2022-05-11
Nova Bus Recalls LFS and LFS Artic Buses Due to Signal Confusion
Nova Bus is recalling 2016-2020 LFS and 2013-2022 LFS Artic buses because a text message board duplicates stop and turn signals, increasing crash risk.
Product
NOVA BUS — NOVA BUS LFS ARTIC, LFS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1029-2022·2022-05-11
Robotic-Assisted Medical Device Recalled Due to Software Defect
The FDA is recalling the VELYS Robotic-Assisted Solution Base due to a software defect in version 1.5.1 related to Daylight Saving Time changes. The defect can cause system errors requiring restart, potentially delaying patient treatment.
Product
VELYS Robotic-Assisted Solution Base Product No.: 451570100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1024-2022·2022-05-11
Siemens ADVIA Centaur Estradiol Test Recalled for Falsely Elevated Results
Siemens Healthcare is recalling all lots of the ADVIA Centaur Enhanced Estradiol diagnostic test because plasma specimens can produce falsely elevated results, potentially leading clinicians to misinterpret patient results.
Product
ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10491445 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1020-2022·2022-05-11
Estradiol diagnostic test kits recalled for falsely elevated results
Siemens Atellica IM Enhanced Estradiol test kits can produce falsely elevated results in plasma specimens, potentially leading to misinterpretation of patient hormone measurements. Approximately 2,044 units worldwide are affected.
Product
Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1025-2022·2022-05-11
Estradiol Diagnostic Device Recalled for Falsely Elevated Test Results
An estradiol diagnostic device has been recalled because it produces falsely elevated test results in plasma specimens. These inaccurate results could cause clinicians to misinterpret patient test results.
Product
ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0834-2022·2022-05-11
Losartan Potassium Tablets Recalled for Excessive Azido Impurity
Macleods Pharma is recalling Losartan Potassium Tablets due to CGMP deviations with azido impurity levels exceeding acceptable limits. The recall affects 5.6 million tablets distributed nationwide.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0831-2022·2022-05-11
Drug recall: Vancomycin HCl injection bags for manufacturing deviations
SCA Pharmaceuticals has recalled Vancomycin HCl 1.5g injection bags due to manufacturing process deviations. The product was distributed nationwide.
Product
Vancomycin HCl 1.5 g in 0.9% Sodium Chloride, 500 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0924-44
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0851-2022·2022-05-11
Erythromycin Topical Gel Recalled Due to Manufacturing Quality Deviations
McKesson Corporation is recalling Erythromycin Topical Gel USP 2% due to CGMP deviations. The manufacturer discontinued its stability study program, prompting a nationwide recall of all products within their expiration date.
Product
Erythromycin Topical Gel USP, 2%, Net Wt 60 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 63739-053-68
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0846-2022·2022-05-11
Lidocaine Oral Topical Solution Recalled Due to Failed Viscosity Specification
Akorn, Inc. is recalling 66,744 bottles of Lidocaine Hydrochloride Oral Topical Solution, USP 2% (Lot #370978) nationwide because the product's viscosity was below the required specification.
Product
Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100 mL per bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701, NDC 50383-775-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1026-2022·2022-05-11
Cervical Cage Trial Kit Recalled for Incorrect Size Labeling
restor3d Inc. is recalling 14 units of its Non-Sterile Double Ended Trial Kit because the product was labeled as Small Footprint when it is actually Medium. The lot was distributed nationwide across seven states.
Product
Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0829-2022·2022-05-11
Norepinephrine Injection Recalled Nationwide for Manufacturing Quality Deviations
SCA Pharmaceuticals recalled 120 bags of Norepinephrine 8mg injection nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall was initiated April 25, 2022.
Product
Norepinephrine 8mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-078-40
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0842-2022·2022-05-11
Losartan Potassium and Hydrochlorothiazide Tablets Recalled for Impurity
Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg tablets nationwide due to AZIDO impurity levels above acceptable limits. Patients should consult their healthcare provider about their medication.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0837-2022·2022-05-11
Losartan Potassium and Hydrochlorothiazide Tablets Recalled Due to AZIDO Impurity Contamination
Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to AZIDO impurity levels exceeding acceptable manufacturing standards. The prescription blood pressure medication was distributed nationwide.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0830-2022·2022-05-11
Drug recall: fentanyl and bupivacaine injectable solution manufacturing deviations
SCA Pharmaceuticals voluntarily recalled 424 bags of fentanyl and bupivacaine injectable solution due to manufacturing control deviations. The product was distributed nationwide in the United States.
Product
Fentanyl 2mcg/ml and Bupivacaine 0.125% in 0.9% Sodium Chloride 100 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0231-32
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V320000·2022-05-10
Land Rover Recalls 2022 New Range Rovers for Front Crash Sensor Defect
Jaguar Land Rover is recalling 2022 New Range Rovers because improperly tightened fasteners may cause front crash sensors to malfunction, affecting air bag deployment.
Product
LAND ROVER — LAND ROVER NEW RANGE ROVER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V318000·2022-05-10
Braxton Creek Recalls 2022 Travel Trailers Due to LP Gas Leak Risk
Braxton Creek RV is recalling 2022 Free Solo, Bushwhacker, and Bushwhacker Plus travel trailers because cracked LP gas fittings may cause a leak and fire.
Product
BRAXTON CREEK — BRAXTON CREEK BUSHWACKER, BUSHWACKER PLUS, FREE SOLO
Category
Vehicle
Distribution
Distributed nationwide