State

American Samoa product recalls

73,503 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 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24751–24775 of 73528

ModerateFDA (Devices)·Z-1679-2021·2021-06-02
Nobel Biocare Implant Crown Recalled for Manufacturing Specification Defects
Nobel Biocare Procera LLC is recalling specific implant crown units because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.
Product
NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77363
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1675-2021·2021-06-02
Roche Recalls Iron Gen 2 Reagent Cassettes Due to Discrepant Results
Roche Diagnostics is recalling 20,468 Iron Gen 2 reagent cassettes because they may produce discrepant elevated results on specific analyzers.
Product
IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for the quantitative determination of iron in human serum and plasma on Roche/Hitachi cobas c and cobas Integra systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1681-2021·2021-06-02
Nobel Biocare Procera LLC Recalls Implant Crowns Not Manufactured to Specification
Nobel Biocare Procera LLC is recalling specific implant crowns because they were not manufactured to specification. The recall affects units distributed in the US and several international countries.
Product
NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77387
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1674-2021·2021-06-02
Siemens Centaur Syphilis Assay Recalled for Potential Carryover Interference
Siemens Healthcare Diagnostics is recalling the Centaur Syphilis Assay-SYP Kit due to potential carryover into other assays on specific systems.
Product
Centaur Syphilis Assay-SYP Kit, 200 Test - Product Usage: For in vitro diagnostic use in the qualitative determination of antibodies to Treponema pallidum in human serum or plasma using the ADVIA Centaur XP/XPT System and ADVIA Centaur CP Systems, SMN:10492493
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0394-2021·2021-06-02
Noven Recalls Daytrana Methylphenidate Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because customer complaints regarding ripped patches and adhesive transfer exceeded action limits.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1678-2021·2021-06-02
Nobel Biocare Procera Implant Crown Recall for Manufacturing Defects
Nobel Biocare Procera LLC is recalling seven implant crown units because they were not manufactured to specification. The recall covers distribution in the US and several international countries.
Product
NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77352
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0564-2021·2021-06-02
Brew Dr. Uplift Drink Recalled Due to Yeast Presence
Brew Dr. Uplift Blood Orange Lemon drink is being recalled because yeast was found in the shelf-stable cans.
Product
Brew Dr. Uplift Blood Orange Lemon, Yerba Mate *Guayusa * Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00870 9. The label is read in parts: "***BLOOD ORANGE LEMON *** YERBA MATE * GUAYUSA * GREEN TEA***BREW DR. UPLIFT…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0563-2021·2021-06-02
Brew Dr. Uplift Blueberry Raspberry Yerba Mate Recalled for Yeast
Brew Dr. Uplift Blueberry Raspberry Yerba Mate is being recalled because yeast was found in the shelf-stable cans.
Product
Brew Dr. Uplift Blueberry Raspberry Yerba Mate Guayusa, Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00867 9. The label is read in parts: "***BLUEBERRY RASPBERRY ***YERBA MATE * GUAYUSA * GREEN TEA***BREW DR UPLIFT ***…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0565-2021·2021-06-02
Brew Dr. Uplift Mango Passionfruit Recalled for Yeast Contamination
Brew Dr. Uplift Mango Passionfruit drinks are being recalled because yeast was found in the product. Consumers should stop drinking the affected cans.
Product
Brew Dr. Uplift Mango Passionfruit, Yerba Mate *Guayusa * Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00871 6. The label is read in parts: "***MANGO PASSIONFRUIT *** YERBA MATE * GUAYUSA * GREEN TEA *** BREW DR. UPLIFT…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1688-2021·2021-06-02
Ortho VITROS CoV2 Ag Calibrator Recalled for Calibration Failures
Ortho-Clinical Diagnostics is recalling 74 units of VITROS CoV2 Ag calibrator (Lot 0020) due to potential unexpected calibration failures.
Product
VITROS CoV2 Ag calibrator (Product Code 6199950) - Product Usage: is a chemiluminescent immunoassay intended for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigens in nasopharyngeal (NP) and anterior nasal swab specimens collected in CDCs formulation of VTM.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0628-2021·2021-06-02
Brill Inc Recalls Chocolate Chip Cookies for Potential Foreign Objects
Brill Inc is recalling specific batches of baked chocolate chip cookies due to the potential presence of small foreign objects.
Product
10239710: 12" BAKED CHOCOLATE CHIP MESSAGE COOKIE 14 / 22 oz BAKED CHOCOLATE CHIP COOKIES KEEP FROZEN AT 0¿F OR BELOW Net weight 19.25 lb (8.73 kg) (14 x 22 oz (624g)) and 10239711 9" CHOCOLATE CHIP BAKED MESSAGE COOKIE 16 / 12.5 oz BAKED CHOCOLATE CHIP COOKIES KEEP FROZEN AT…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1680-2021·2021-06-02
Nobel Biocare Procera Implant Crown Recalled for Manufacturing Defect
Nobel Biocare Procera LLC is recalling specific implant crown units that were not manufactured to specification. The recall affects units distributed in the US and several international countries.
Product
NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics. Material Number: 77364
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0393-2021·2021-06-02
Noven Recalls Daytrana Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because customer complaints regarding ripped patches and adhesive issues exceeded action limits.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1677-2021·2021-06-02
Nobel Biocare Procera Recalls Two Dental Implant Crowns for Specification Defects
Nobel Biocare Procera LLC is recalling two dental implant crown units because they were not manufactured to specification. The affected units were distributed in the US and several international countries.
Product
NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw creating a prosthetic device (full contour crown), and to restore the patient s chewing function and esthetics Material Number: 77339
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0392-2021·2021-06-02
Ascend Recalls Olmesartan Medoxomil Tablets Due to Foreign Tablet Presence
Ascend Laboratories LLC is recalling 34,296 bottles of Olmesartan Medoxomil 20 mg tablets because they may contain a foreign tablet or capsule.
Product
OLMESARTAN MEDOXOMIL — OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0599-2021·2021-06-02
Dr. Reddy's Recalls Atorvastatin Calcium Tablets Due to Impurities
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium 10 mg tablets due to the presence of degradation impurities.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·21V409000·2021-06-01
Altec Aerial Devices Recalled for Boom Spool Shift Risk
Altec is recalling 2005-2021 aerial devices because boom spools can shift, increasing injury risk. Owners should contact Altec for free repairs.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V408000·2021-06-01
Custom Truck Recalls 2020 Ford F-550 Vehicles Due to Display Defect
Custom Truck is recalling 2020 Ford F-550 vehicles because LCD displays may lock up, potentially delaying emergency efforts.
Product
CUSTOM TRUCK & BODY WORKS — CUSTOM TRUCK & BODY WORKS FORD F-550
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V407000·2021-05-29
Ford Recalls 2021 F-150 Trucks Due to Steering Gear Defect
Ford is recalling 2021 F-150 vehicles because internal steering gear damage could cause loss of steering control. Owners should not drive until the repair is complete.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V406000·2021-05-28
2021 Mercedes-Benz Cabriolets: Rear Headrests May Be Incorrectly Mounted
Mercedes-Benz USA is recalling approximately 218 2021 Cabriolet models due to rear headrests that may be incorrectly mounted to the seatbacks. The headrests could move or detach during a crash, increasing the risk of injury.
Product
MERCEDES-BENZ — MERCEDES-BENZ C 300, E 450, AMG E53, AMG C43
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V403000·2021-05-28
Mercedes-Benz Recalls 2020 GLB 250 Vehicles for Water Intrusion Defect
Mercedes-Benz is recalling 2020 GLB 250 vehicles because water may enter the foot wells, potentially causing electrical damage, engine stalls, or a blank instrument cluster.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLB 250
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V405000·2021-05-28
Mercedes-Benz Recalls 2020 GLB 250 Vehicles for Air Bag Defect
Mercedes-Benz is recalling 2020 GLB 250 vehicles because the front passenger air bag may tear upon deployment, increasing injury risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLB 250
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V404000·2021-05-28
Mercedes-Benz Recalls 2020 GLB 250 for Side Air Bag Defect
Mercedes-Benz is recalling 2020 GLB 250 vehicles because side curtain air bags may not deploy properly in a crash, increasing injury risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLB 250
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V401000·2021-05-27
BMW Recalls 3 Series Vehicles for Air Bag Inflator Defect
BMW is recalling 1999-2001 3 Series vehicles because the driver-side air bag inflator may explode or underinflate, posing a risk of serious injury.
Product
BMW — BMW 330CI, 3 SERIES, 328CI, 330I
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V402000·2021-05-27
2021 INFINITI QX50 Steering Knuckle Structural Defect - Multiple Models Affected
Nissan recalls 2021 INFINITI QX50 and other vehicles due to front steering knuckles and rear axle housings with insufficient strength from improper heat treatment, which could deform on impact and cause loss of steering control or wheel separation.
Product
INFINITI — INFINITI, NISSAN QX60, MURANO, Q50, GT-R
Category
Vehicle
Distribution
Distributed nationwide