State

American Samoa product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34376–34400 of 73763

SevereFDA (Drugs)·D-1033-2019·2019-03-27
Advanced Pharma Recalls Morphine Sulfate Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 2,325 syringes of Morphine Sulfate 30 mg/30 mL Injectable Solution nationwide due to a lack of assurance of sterility.
Product
Morphine Sulfate 30 mg/30 mL (1 mg/mL) Injectable Solution Morphine Sulfate 30 mg 0.9% Sodium Chloride QS 30 mL Sterile singe use syringe, NDC: 42852-241-63 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1028-2019·2019-03-27
Advanced Pharma Recalls Phenylephrine HCl Injectable Syringes for Sterility Concerns
Advanced Pharma Inc. is recalling 800 syringes of Phenylephrine HCl Injectable Solution due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Phenylephrine HCl, 800 mcg in 0.9% Sodium Chloride, QS 10 mL Injectable Solution, 800 mcg/10 mL (80 mcg per mL), 10mL Sterile single use syringe, NDC: 42852-865-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1047-2019·2019-03-27
Valsartan Tablets Recalled Due to Carcinogenic Impurity
American Health Packaging is recalling Valsartan Tablets 160 mg because a carcinogenic impurity was detected in the active ingredient.
Product
Valsartan Tablets USP 160 mg, 100 Tablets (10 x 10) per Unit Dose Blisters, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217 (Individual Dose NDC:60687-139-11, Carton NDC#: 60687-139-01)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1024-2019·2019-03-27
Advanced Pharma Recalls Neostigmine Methylsulfate Injection Due to Sterility Concerns
Advanced Pharma Inc. is recalling 5,700 syringes of Neostigmine Methylsulfate Injection Solution because there is a lack of assurance of sterility.
Product
Neostigmine Methylsulfate Injection Solution 5 mg/5mL (1 mg per mL), 5mL Sterile single use syringe, For IV use only, NDC: 42852-829-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1042-2019·2019-03-27
Camber Pharmaceuticals Recalls Losartan Potassium Tablets Due to NMBA Contamination
Camber Pharmaceuticals is recalling Losartan Potassium tablets because trace amounts of the impurity NMBA were detected in the active ingredient.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1046-2019·2019-03-27
AvKARE Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity
AvKARE Inc. is recalling Losartan Potassium and Hydrochlorothiazide Tablets because an impurity, N-Methylnitrosobutyric acid (NMBA), was identified.
Product
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/12.5 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only Manufactured for: AvKARE Inc. Pulaski, TN 38478 --- NDC 50268-514-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1029-2019·2019-03-27
Advanced Pharma Recalls Esmolol HCl Injectable Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 550 syringes of Esmolol HCl Injectable Solution due to a lack of assurance of sterility. The affected products were distributed nationwide.
Product
Esmolol HCl Injectable Solution 100 mg/10 mL (10 mg per mL)10mL Sterile single use syringe, NDC: 42852-827-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1031-2019·2019-03-27
Advanced Pharma Recalls Heparin Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,440 syringes of Heparin 5,000 Units/5mL Injectable Solution nationwide due to a lack of assurance of sterility.
Product
Heparin 5,000 Units/5mL (1,000 Units per mL) Injectable Solution, 5,000 Units in 0.9% Sodium Chloride, QS 5 mL Sterile single use syringe, NDC: 42852-739-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1044-2019·2019-03-27
AvKARE Recalls Losartan Potassium Tablets Due to Impurity
AvKARE Inc. is recalling Losartan Potassium Tablets 50 mg because an impurity, N-Methylnitrosobutyric acid (NMBA), was identified.
Product
Losartan Potassium Tablets USP 50 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only, Manufactured for: AvKARE Inc. Pulaski, TN 38478 ---- NDC 50268-517-15
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1023-2019·2019-03-27
Advanced Pharma Recalls Phenylephrine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 22,900 syringes of Phenylephrine HCl injectable solution nationwide due to a lack of assurance of sterility.
Product
Phenylephrine HCl, 1 mg in 0.9% Sodium Chloride, QS 10 mL Injectable Solution 1 mg/10 mL (100 mcg per mL), Sterile single use syringe, NDC: 42852-830-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1043-2019·2019-03-27
Camber Pharmaceuticals Recalls Losartan Potassium Tablets Due to NMBA Contamination
Camber Pharmaceuticals is recalling Losartan Potassium tablets because trace amounts of the nitrosamine NMBA were detected in the active ingredient.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1034-2019·2019-03-27
Advanced Pharma Recalls Phenylephrine Injectable Solution Due to Sterility Concerns
Advanced Pharma Inc. is recalling 975 units of Phenylephrine HCl injectable solution due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Phenylephrine HCl, 1,200 mcg in 0.9% Sodium Chloride, QS 10 mL Injectable Solution 1,200 mcg/10 mL (120 mcg per mL), Sterile single use syringe, NDC: 42852-882-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1013-2019·2019-03-27
Mylan Recalls Alprazolam Tablets Due to Elevated Impurity Levels
Mylan Institutional, Inc. is recalling specific lots of Alprazolam Tablets, 0.25 mg, because elevated levels of a known impurity were detected during stability testing.
Product
Alprazolam Tablets, USP, 0.25 mg, 10x10 per carton, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-788-20
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1030-2019·2019-03-27
Advanced Pharma Recalls Heparin Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 500 syringes of Heparin 10 Units/10 mL due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Heparin 10 Units/10 mL 10 Units in 0.45% Sodium Chloride, QS 10 mL, Injectable Solution, Dwell, 10mL Sterile single use syringe, NDC: 42852-725-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1182-2019·2019-03-27
Nova Salted Biscuit Recalled for Undeclared Milk Allergen
Asia Food Distributor is recalling Nova Salted Biscuit because the product contains undeclared milk. Consumers should check their pantries for the specific lot.
Product
Nova Salted Biscuit The product comes in a 14.08 ounce, paper box marked with manufacturing date of Apr 2018 and expiration date of June 2020 stamped on the side.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1020-2019·2019-03-27
Advanced Pharma Recalls Phenylephrine HCl Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 16,075 syringes of Phenylephrine HCl injectable solution nationwide due to a lack of assurance of sterility.
Product
Phenylephrine HCl, 500 mcg in 0.9% Sodium Chloride, QS 5 mL Injectable Solution 500 mcg/5 mL (100 mcg per mL), 5mL Sterile single use syringe, NDC: 42852-830-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1027-2019·2019-03-27
Advanced Pharma Recalls Lidocaine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,980 syringes of 2% Lidocaine HCl Injectable Solution nationwide due to a lack of assurance of sterility.
Product
2% Lidocaine HCl Injectable Solution, 100 mg/5 mL (20 mg per mL), 5mL Sterile single use syringe, NDC: 42852-011-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1018-2019·2019-03-27
Advanced Pharma Recalls Fentanyl Injectable Solution Due to Sterility Concerns
Advanced Pharma Inc. is recalling 180 bags of fentanyl injectable solution nationwide due to a lack of assurance of sterility.
Product
fentaNYL 2500 mcg/250 mL Injectable Solution, Fentanyl 0.9% Sodium Chloride, QS, Sterile single use bags, NDC: 42852-210-25 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1022-2019·2019-03-27
Advanced Pharma Recalls Phenylephrine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,575 syringes of Phenylephrine HCl injectable solution because the company cannot guarantee the product is sterile.
Product
Phenylephrine HCl, 400 mcg in 0.9% Sodium Chloride, QS 10 mL Injectable Solution 400 mcg/10 mL (40 mcg per mL), Sterile single use syringe, NDC: 42852-876-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1026-2019·2019-03-27
Advanced Pharma Recalls Lidocaine Syringes Due to Sterility Concerns
Advanced Pharma Inc. is recalling 1,540 syringes of 2% Lidocaine HCl Injectable Solution because the company cannot assure the product's sterility.
Product
2% Lidocaine HCl Injectable Solution, 60 mg/3 mL (20 mg per mL), 3mL Sterile single use syringe, NDC: 42852-011-22 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1039-2019·2019-03-27
Shimadzu Mobile X-Ray System Recalled for Brake Failure
Shimadzu is recalling 93 MobileDaRt Evolution mobile X-ray systems because the brakes may fail to engage when the operator releases the drive handle.
Product
SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1065-2019·2019-03-27
Heritage Pharmaceuticals Recalls Subpotent Etomidate Injection Vials
Heritage Pharmaceuticals is recalling 11,888 vials of Etomidate Injection because the drug was found to be subpotent. The recall is voluntary and nationwide.
Product
Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1040-2019·2019-03-27
Fujifilm FDR Go PLUS Mobile X-Ray System Recalled for Braking Defect
Fujifilm is recalling 56 mobile X-ray systems because the braking mechanism may fail to engage when the handle is released.
Product
Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V240000·2019-03-27
Thor Motor Coach Recalls 2018-2020 Models Due to Reversed Backup Camera Image
Thor Motor Coach is recalling 110 motorhomes because the backup camera image may reverse, increasing crash risk. Dealers will install a harness to fix the issue.
Product
THOR MOTOR COACH — THOR MOTOR COACH CHATEAU, MAGNITUDE, FOUR WINDS, OMNI
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1036-2019·2019-03-27
ConvaTec Recalls Feeding Tubes Due to Potential Sterile Barrier Breach
ConvaTec is recalling specific lots of Feeding Tube Metric devices because an internal assessment found a potential breach in the sterile barrier.
Product
Feeding Tube Metric, disposable, sterile, 100 eaches per sales unit. Labeled as: xray CH05/40CM and xray CH08/40CM Product Usage: Duodenal and Stomach Gastroenterology Tubes are sterile disposable devices which may be inserted through the nose or mouth via the esophagus into…
Category
Medical Device
Distribution
Distributed nationwide