State

American Samoa product recalls

73,366 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 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19626–19650 of 73391

HighFDA (Devices)·Z-1448-2022·2022-07-27
Cervical spinal implant connectors may fail to maintain proper clamping force
Aesculap Implant Systems has recalled certain cervical spine implant connectors due to insufficient clamping force. The defect may allow movement on the rods or cause microparticle abrasion.
Product
AESCULAP S4 Cervical Cross Connector L 42-58mm, S4C CROSS CONNECTOR VARIABLE 42-58MM, product code SW117T. Used in spinal fusion surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1435-2022·2022-07-27
BD Connecta Stopcock Without Extension Tube Recalled for Potential Leakage Risk
Becton Dickinson & Company is recalling BD Connecta Stopcock units worldwide due to a potential housing leakage defect that could interrupt treatment or cause exposure to biohazardous material.
Product
BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1416-2022·2022-07-27
Hill-Rom Centrella Pro+ mattress reduced heat-moisture management performance
Affected Hill-Rom Centrella Pro+ 36-inch mattresses may have reduced Microclimate Management performance, increasing risk of pressure ulcer development. The failure affects heat and moisture control.
Product
Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1251-2022·2022-07-27
Epinephrine Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling 134,385 epinephrine injection syringes nationwide due to lack of assurance of sterility. No illnesses have been reported.
Product
EPINEPHrine Injection, USP, 1 mg/10 mL (100 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-925-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1276-2022·2022-07-27
Nephron Phenylephrine HCl Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center LLC recalls Phenylephrine HCl Injection (1 mg/10 mL) syringes nationwide due to inability to guarantee sterility. Approximately 464,265 syringes across eleven lot numbers are affected.
Product
Phenylephrine HCl Injection, USP, 1 mg/10 mL (100 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-957-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1268-2022·2022-07-27
Morphine Sulfate Injection Recalled Due to Sterility Assurance Concerns
Nephron Sterile Compounding Center LLC is recalling morphine sulfate injection syringes due to lack of assurance of sterility. The recall affects 4,620 pre-filled syringes distributed nationwide.
Product
Morphine Sulfate Injection, USP, 1 mg/mL syringe, packaged in 5 x 1 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-979-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1403-2022·2022-07-27
Radiation treatment planning software fails to propagate treatment course data
RayStation 9B SP1 radiation treatment planning software has an issue where treatment course information may not be propagated to other systems in some workflows. This could potentially affect treatment planning accuracy.
Product
RayStation 9B SP1. For radiation treatment planning.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1496-2022·2022-07-27
Truffle Dark Gift Box Recalled for Undeclared Tree Nuts
Queen Bee Gardens recalls Truffle Dark Gift Box due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product poses a risk to consumers with tree nut allergies.
Product
Truffle Dark Gift Box, 12 pc., 6 oz. PLU Code: 788394 17660 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1486-2022·2022-07-27
Honeymoons Dark Chocolate Cashew Recalled for Undeclared Tree Nuts
Honeymoons Dark Chocolate Cashew products may contain undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product is being recalled from Queen Bee retail locations in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Honeymoons Dark Chocolate Cashew. PLU Code: 788394 14864 4.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1488-2022·2022-07-27
Honeymoons Milk Chocolate Pecan recalled for undeclared tree nuts
Queen Bee Gardens is recalling Honeymoons Milk Chocolate Pecan candies due to the potential presence of undeclared tree nuts. Consumers with tree nut allergies should not consume this product.
Product
Honeymoons Milk Chocolate Pecan. PLU Code: 788394 14684 8. Ingredients: Honey, milk chocolate (sugar, milk, cocoa butter, chocolate liquor, sunflower lecithin and pure vanilla), pecans, butter (pasteurized cream, salt) cream, nonfat dry milk, whey, sunflower lecithin, algin…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1283-2022·2022-07-27
FDA Recalls Cipla Difluprednate Eye Drops for Defective Container Caps
Cipla is recalling 8,136 bottles of Difluprednate ophthalmic emulsion nationwide due to defective container caps that can break and expose the medication tip, compromising sterility.
Product
DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1433-2022·2022-07-27
BD Connecta Stopcock Recalled for Potential Housing Leakage
Becton Dickinson is recalling approximately 1.96 million BD Connecta Stopcock devices due to potential leakage at the housing component, which could interrupt treatment and expose patients to biohazardous material.
Product
BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1498-2022·2022-07-27
Chocolate Sampler product recalled due to undeclared tree nuts
Queen Bee Gardens is recalling Chocolate Sampler 13 oz packages due to undeclared tree nuts. The products may contain pecans, almonds, coconut, macadamia nuts, or walnuts.
Product
Chocolate Sampler Net wt. 13 oz. PLU Code: 788394 76511 7
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1443-2022·2022-07-27
Spinal Fusion Implant Cross Connectors Recalled for Insufficient Clamping Force
Aesculap is recalling its S4 Cervical Cross Connector used in spinal fusion surgery due to insufficient clamping force that may cause the connectors to move on the rods or shed particles.
Product
AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code SW112T. Used in spinal fusion surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1462-2022·2022-07-27
Macadamia Classic Truffles Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Macadamia Classic Truffles because they may contain undeclared tree nuts including almonds, coconut, and walnuts. The product poses allergen risks to consumers with tree nut allergies.
Product
Macadamia Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11060 3. Ingredients: Milk chocolate (sugar, milk, cocoa butter, chocolate liquor, soya lecithin and pure vanilla) honey, butter (pasteurized cream, salt), cream, roasted & sea salted macadamias, pecans, non-fat dry…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1273-2022·2022-07-27
Oxytocin Injectable Recalled Due to Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Oxytocin 30 Units/500 mL injectable solution due to lack of sterility assurance. Approximately 1,810 bags with lot codes OX2013C and OX2013E were distributed nationwide.
Product
Oxytocin 30 Units/500 mL (0.06 Units/mL) in 0.9% Sodium Chloride Injection, USP IV bag, packaged in 10 x 1 IV Bag per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-543-50
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V541000·2022-07-27
2022-2023 BMW IX and i4 High-Voltage Battery Fire Risk Recall
Certain 2022-2023 BMW IX and 2022 i4 vehicles are recalled due to high-voltage batteries that may develop internal damage and short-circuit, posing a fire risk. Owners should not drive or charge the vehicle until the battery is replaced.
Product
BMW — BMW IX, I4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1451-2022·2022-07-27
Almond Coconut Truffles Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Almond Coconut Classic Truffles for undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The affected product was sold in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Almond Coconut Classic Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11025 2. Ingredients: Milk & dark chocolate, honey, butter (pasteurized cream & salt), cream, coconut, almonds, non-fat dry milk, whey, natural flavors, agar, algin & lecithin. Note: Typo on website should be…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1256-2022·2022-07-27
HYDROmorphone HCl Injection Syringes Recalled for Sterility Assurance
Nephron Sterile Compounding Center is recalling HYDROmorphone HCl Injection syringes nationwide due to lack of assurance of sterility. The recall affects 12,900 syringes across two manufacturing lots.
Product
HYDROmorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL) syringes, 5 x 30 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-529-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1456-2022·2022-07-27
Chocolate Truffles Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Dark on Dark Classic Truffle products due to the potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts) that pose an allergen risk to sensitive consumers.
Product
Dark on Dark Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11030 6. Ingredients: Dark chocolate, honey, butter (pasteurized cream & salt), cream, non-fat dry milk, whey, agar, algin & lecithin.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1249-2022·2022-07-27
Compounded Injectable Medications Recalled for Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling 2,315 pre-filled syringes due to lack of sterility assurance. The compounded injectable medication was distributed nationwide.
Product
Bupivacaine HCl 150 mg (3.0 mg/mL), Ketorolac Tromethamine 60 mg (1.2 mg/mL), Ketamine HCl 60 mg (1.2 mg/mL) Injection, 50 mL syringes, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St.…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1468-2022·2022-07-27
QBee Sea Salt Caramel Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling QBee Sea Salt Caramel due to undeclared tree nuts. The affected product was sold at ten retail locations in Colorado, New Mexico, and Wyoming, and via internet sales.
Product
QBee Sea Salt Caramel. Net wt. 1 oz. PLU Code: 788394 11010 8.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1434-2022·2022-07-27
BD Connecta Stopcock recalled for potential housing leakage risk
Becton Dickinson is recalling BD Connecta Stopcocks due to potential leakage at the housing component. The defect may interrupt treatment and expose patients to biohazardous material.
Product
BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1279-2022·2022-07-27
Sodium Bicarbonate Injection USP recalled for lack of sterility assurance
Nephron Sterile Compounding Center recalls 36,354 pre-filled syringes of Sodium Bicarbonate Injection due to lack of sterility assurance. The medication was distributed nationwide.
Product
8.4% Sodium Bicarbonate Injection, USP, 4.2 g/50 mL (84 mg/mL) 1 mEq/mL syringe, packaged in 1 x 50 mL Pre-Filled Syringe per carton, 30 x 1 syringe carton per case, Rx Only Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-214-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1411-2022·2022-07-27
Medical Device Recall: Hill-Rom PRO+ Mattress Microclimate Feature Failure
Hill-Rom PRO+ mattresses are being recalled for a Microclimate Management feature failure that could increase pressure ulcer risk in patients. The recall affects 200 units distributed in the US and Canada.
Product
Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.
Category
Medical Device
Distribution
Distributed nationwide