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.

52376–52400 of 73858

SevereFDA (Drugs)·D-1366-2015·2015-09-02
Mucinex Fast-Max Liquid Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.
Product
Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Time Cold & Flu Two - 6 fl oz (180 mL) bottles Total -12 fl oz (360 mL), For Age 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC 63824-526-22
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1364-2015·2015-09-02
Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast Max Night Time Cold & Flu liquid bottles because the back label is missing active ingredients and safety warnings.
Product
Mucinex Fast Max Night Time Cold & Flu, Maximum Strength, Acetaminophen Pain Reliever/Fever Reducer, Diphenhydramine HCl Antihistamine/Cough Suppressant, Phenylephrine HCl Nasal Decongestant, 6 fl oz. (180 mL) Bottle, For Ages 12+, Dist. By: Reckitt Benckiser Parsippany, NJ…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1367-2015·2015-09-02
Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast Max liquid bottles where the back label is missing active ingredients and safety warnings.
Product
Mucinex Fast Max Severe Congestion & Cough, Maximum Strength, Dextromethorphan HBr Cough Suppressant, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Age 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224, Made in India, NDC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1361-2015·2015-09-02
GlaxoSmithKline Recalls Bactroban Cream Due to Penicillin Contamination
GlaxoSmithKline is recalling Bactroban Cream (mupirocin calcium) 2% because the product was contaminated with penicillin and foreign substances during manufacturing.
Product
Bactroban Cream (mupirocin calcium), 2%, a) 15g tube ( NDC 0029-1527-22), b) 30g tube (NDC 0029-1527-25), Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2374-2015·2015-09-02
Ethicon Recalls SEDASYS Sedation Systems Due to Plastic Degradation
Ethicon is recalling 14 SEDASYS Computer-Assisted Personalized Sedation Systems because unspecified disinfecting methods caused the plastic material of the Control Unit to degrade.
Product
SEDASYS Computer-Assisted Personalized Sedation System, SEDPRU01. An integrated physiological monitoring and drug delivery system intended to provide physician-led teams with a means of administering 1% propofol (10 mg/mL) injectable emulsion to sedate patients > 18 (ASA…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1359-2015·2015-09-02
Bactroban Nasal Ointment Recalled for Penicillin Contamination
GlaxoSmithKline is recalling Bactroban Nasal Ointment due to penicillin cross-contamination and foreign substances found during manufacturing.
Product
Bactroban (mupirocin calcium) Nasal Ointment, 2% 1g tube, Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217. NDC 0029-1526-11
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1368-2015·2015-09-02
Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling
Reckitt Benckiser is recalling Mucinex Fast Max liquid bottles because the back label is missing active ingredients and safety warnings.
Product
Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu, Maximum Strength, Two - 6 fl oz (180 mL) bottles Total - 12 fl oz (360 mL), For Ages 12+, Dist. by Reckitt Benckiser Parsippany, NJ 07054-0224, Made in India, NDC 63824-528-22-01, NDC 63824-528-22-00, UPC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1360-2015·2015-09-02
Bactroban Ointment Recalled for Penicillin Contamination and Foreign Substances
GlaxoSmithKline is recalling Bactroban Ointment due to penicillin cross-contamination and foreign substances found during manufacturing.
Product
Bactroban Ointment (mupirocin calcium), 2% 22g tube ,Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217. NDC 0029-1525-44
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1362-2015·2015-09-02
GlaxoSmithKline Recalls Mupirocin Calcium Cream Due to Penicillin Contamination
GlaxoSmithKline is recalling Mupirocin Calcium Cream, 2%, because the product was contaminated with penicillin and foreign substances during manufacturing.
Product
Mupirocin Calcium Cream, 2%, a) 15g tube (NDC 66993-942-15),b) 30g tube (NDC 66993-942-31), Rx only, Manufactured by Glaxo Operations UK Ltd, Harmire Road, Barnard Castle, UK for GlaxoSmithKline PO Box 1217 Zebulon, NC 27597-1217.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1355-2015·2015-09-02
PharMEDium Recalls Heparin Sodium Injection Bags Due to Particulate Matter
PharMEDium Services is recalling 480 bags of Heparin Sodium Injection USP due to the presence of particulate matter. The product was distributed nationwide.
Product
HEPARIN Sodium Injection USP, 12,500 USP Units added to 250 mL 5% Dextrose Injection USP (50 units per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K0418, NDC# 61553-418-02.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V552000·2015-09-02
Forest River Recalls 2016 Shasta Airflyte Trailers Due to Tire Clearance Defect
Forest River is recalling 2016 Shasta Airflyte 16 and 19 trailers because insufficient tire clearance may cause tire failure and increase crash risk.
Product
SHASTA — SHASTA AIRFLYTE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1353-2015·2015-09-02
Pharmedium Recalls Oxytocin Injection Bags Due to Particulate Matter
Pharmedium Services, LLC is recalling 72 bags of oxyTOCIN 15 Units in 5% Dextrose Injection due to the presence of particulate matter.
Product
oxyTOCIN 15 Units added to 250 mL 5% Dextrose Injection USP, packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K2677, NDC# 61553-777-02.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V551000·2015-09-02
Foretravel Recalls 2012-2014 Motorhomes Due to Loose Front Ball Joints
Foretravel is recalling 2012-2014 Nimbus, Phenix, and IH45 motorhomes because loose front ball joints may separate, causing loss of steering control and increasing crash risk.
Product
FORETRAVEL — FORETRAVEL NIMBUS, IH45, PHENIX
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2451-2015·2015-09-02
Synthes Trauma Ex-Fix System Recalled for MR Labeling Corrections
Synthes (USA) Products LLC is recalling the Trauma Ex-Fix System to correct MRI safety labeling. The recall identifies additional part numbers as MR Conditional and notes one serious injury.
Product
Synthes Trauma Ex-Fix System (Small, Medium, Distraction Osteogenesis (DO) and Large) ; (S) intended to stabilize and provide treatment for fractures of the small bones, such as the hand, wrist, forearm, foot, and ankle; (M) for the construction of an external fixation frame for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2462-2015·2015-09-02
Arrow International Recalls PICC Kits with Potential Peel-Away Sheath Defect
Arrow International is recalling 52,109 PICC kits because the peel-away sheath hub tabs may prematurely detach. One injury has been reported.
Product
PICC Kits with Peel-Away Sheath Component; catheter, intravascular, therapeutic, ultrasound Product Usage: catheter, intravascular, therapeutic, ultrasound
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2456-2015·2015-09-02
Trilliant Surgical Reamer Heads Recalled for Guide Pin Fit Issues
Trilliant Surgical Ltd. is recalling 638 Concave and Convex Reamer Heads because the cannulation may be too small to allow the Guide Pin to pass through freely.
Product
Concave Reamer Head, 16 mm; Concave Reamer Head, 18 mm; Concave Reamer Head, 20 mm; Concave Reamer Head 22 mm; Convex Reamer Head, 16 mm; Convex Reamer Head, 18 mm; Convex Reamer Head 20 mm; Convex Reamer Head 22 mm, used with Gridlock Plating system, for use in trauma and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2447-2015·2015-09-02
Roche cobas b 123 Fluid Pack Recall for Low PO2 Results
Roche is recalling 82 cobas b 123 Fluid Packs due to a calibration issue that may cause erroneously low PO2 results in patient samples.
Product
cobas b 123 Fluid Pack COOX REF 05170036001 400 Product Usage: The cobas b 123 POC system is a fully automated POC system for whole blood in vitro measurement of pH, blood gases (B3G), electrolytes NAT, K+, iCaWt (ISE), hematocrit (THct), metabolites (GLu, Lac) total…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2470-2015·2015-09-02
GE Healthcare Recalls Centricity Universal Viewer Software Due to Image Loss
GE Healthcare is recalling 26 Centricity Universal Viewer Version 6.0 systems because medical images may be missing when a specific system parameter is set to a value greater than 1.
Product
Centricity Universal Viewer Product Usage: The Centricity Universal Viewer Version 6.0 software is a picture archiving and communications system, a device that provides one or more capabilities relating to the acceptance, transfer, display, storage, and digital processing of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2446-2015·2015-09-02
Roche cobas b 123 Fluid Pack Recall for Low PO2 Results
Roche is recalling 82 cobas b 123 Fluid Packs due to a calibration issue that may cause erroneously low PO2 results in patient samples.
Product
cobas b 123 Fluid Pack COOX REF 05169992001 200 Product Usage: The cobas b 123 POC system is a fully automated POC system for whole blood in vitro measurement of pH, blood gases (B3G), electrolytes NAT, K+, iCaWt (ISE), hematocrit (THct), metabolites (GLu, Lac) total…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2455-2015·2015-09-02
Omnilife Recalls Offset Femoral Alignment Guides Due to Incorrect Markings
Omnilife Science Inc. is recalling 15 Offset Femoral Alignment Guides because the markings are reversed, which may prevent proper alignment during surgery.
Product
Offset Femoral Alignment Guide 4mm x 6¿; Product Code: KS 67024 Product Usage: The instrumentation has been designed to facilitate bone preparation and implantation of the Apex Knee or Apex Hip Systems. Product Usage: The instrumentation has been designed to facilitate…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1352-2015·2015-09-02
Unichem Recalls Hydrochlorothiazide Tablets Due to Foreign Tablet Presence
Unichem Pharmaceuticals is recalling 4,776 bottles of hydrochlorothiazide 25 mg tablets because a pharmacist found a clopidogrel tablet in one bottle.
Product
HYDROCHLOROTHIAZIDE — HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2454-2015·2015-09-02
Omnilife Recalls Offset Femoral Alignment Guides Due to Incorrect Markings
Omnilife Science Inc. is recalling 15 Offset Femoral Alignment Guides because the markings are reversed, which may prevent proper alignment during surgery.
Product
Offset Femoral Alignment Guide, 2mm x 6¿; Product Code: KS 67022 Product Usage: The instrumentation has been designed to facilitate bone preparation and implantation of the Apex Knee or Apex Hip Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2443-2015·2015-09-02
Recall of Infant Heel Warmers Due to Potential Breakage and Spillage
The FDA is recalling 68,800 units of Infant Heel Warmers because they may break during activation, causing spillage of contents that could irritate skin or eyes.
Product
Covidien Argyle Infant Heel Warmers (no tab) Item Code: MH00002N Product Usage: Intended for application of the right amount of heat to an infants heel for blood sampling
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2444-2015·2015-09-02
FDA Recalls Covidien Infant Heel Warmers Due to Breakage Risk
The FDA is recalling 164,749 units of Covidien Infant Heel Warmers because they may break during activation, causing spillage and potential skin or eye irritation.
Product
Covidien Argyle Infant Heel Warmers (with tab) Item Code: MH00002T Product Usage: Intended for application of the right amount of heat to an infants heel for blood sampling.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2467-2015·2015-09-02
Sunrise Medical Recalls Quickie IRIS Wheelchairs with Dynamic Backrest
Sunrise Medical is recalling 64 Quickie IRIS wheelchairs because the backrest system may break, posing a risk of falls or injury to the occupant.
Product
Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code 183M02 - MONO Backrest system with Dynamic Backrest option. Provide mobility to persons limited to a sitting position.
Category
Medical Device
Distribution
Distributed nationwide