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.

19601–19625 of 73391

HighFDA (Drugs)·D-1265-2022·2022-07-27
Morphine Sulfate Injection Recalled for Lack of Sterility Assurance
Nephron Sterile Compounding Center is recalling Morphine Sulfate Injection due to lack of assurance of sterility. The recall affects 5,495 pre-filled syringes distributed nationwide.
Product
Morphine Sulfate Injection, USP, 50 mg/50 mL (1 mg/mL) syringe, 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. Extension, West Columbia, SC 29172, NDC: 69374-979-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1477-2022·2022-07-27
Honey Caramels Huckleberry Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honey Caramels Huckleberry (5.87 oz) because they may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. This poses a serious health risk to people with tree nut allergies.
Product
Honey Caramels Huckleberry. Net wt. 5.87 oz. PLU Code: 788394 12623 9. Ingredients: Honey, butter (pasteurized cream & salt), cream, nonfat dry milk, natural flavors, purple cabbage (coloring), whey, lecithin, algin & agar.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1339-2022·2022-07-27
Dietary Supplement Marketed as Unapproved Drug Recalled by FDA
Launch Sequence Capsules, a dietary supplement sold in 60-count bottles, were recalled because they were marketed without FDA approval as a drug based on label claims.
Product
Launch Sequence Capsules, Dietary Supplement, 60- count bottles, ASIN B07TLPWXDS, UPC Code 641378938375.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1492-2022·2022-07-27
Honeymoon Cinna-Bee Patties recalled due to undeclared tree nuts
Queen Bee Gardens is recalling Honeymoon Cinna-Bee Patties due to potential undeclared tree nuts: pecans, almonds, coconut, macadamia nuts, and walnuts. Products were distributed in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Honeymoon Cinna-Bee Patties. PLU Code: 788394 14892 7
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1483-2022·2022-07-27
Honeymoons Milk Chocolate Almond Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honeymoons Milk Chocolate Almond candy due to undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product was distributed in Colorado, New Mexico, Wyoming, and nationwide online.
Product
Honeymoons Milk Chocolate Almond. PLU Code: 788394 14756 2.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1490-2022·2022-07-27
Honeymoons Ivory Chocolate Pecan Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honeymoons Ivory Chocolate Pecan due to undeclared tree nuts, which may affect consumers with tree nut allergies. The product was sold at retail locations in Colorado, New Mexico, and Wyoming, plus nationwide internet sales.
Product
Honeymoons Ivory Chocolate Pecan. PLU Code: 788394 14730 0
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1285-2022·2022-07-27
Aripiprazole 20mg Tablets Recalled for Failed Dissolution
Apotex Corp. is recalling 2,010 bottles of Aripiprazole Tablets 20mg nationwide due to failed dissolution specifications. Tablets may not dissolve properly, potentially affecting medication effectiveness.
Product
Aripiprazole Tablets, USP 20 mg, packaged in a) 1,000-count bottle (NDC 60505-2676-8, UPC 3 60505 26768 2), b) 30-count bottle (NDC 60505-2676-3, UPC 3 60505 26763 7), Rx only, Manufactured by: Apotex, Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston…
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V542000·2022-07-27
2022 Volkswagen Golf R Sunroof Switch May Close Unexpectedly
Volkswagen is recalling certain 2022 Golf R and Golf GTI vehicles because the sunroof touch switch may be too sensitive and inadvertently pressed, causing unintended sunroof auto-closure and risking injury.
Product
VOLKSWAGEN — VOLKSWAGEN GTI, GOLF R
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1499-2022·2022-07-27
Dark Raspberry Classic Snack Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Dark Raspberry Classic snacks due to undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts) that may be present, posing a risk to consumers with tree nut allergies.
Product
Dark Raspberry Classic. Net wt. 1.4 oz. UPC 788394 10003 1.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1441-2022·2022-07-27
Nexiva IV Catheter Stopcock May Leak During Infusion
Becton Dickinson is recalling specific lots of Nexiva IV catheters because the stopcock housing may leak, potentially interrupting treatment and exposing patients to infusate and biohazardous material.
Product
Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Catalog No.383682 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1258-2022·2022-07-27
FDA Recalls HYDROmorphone Injection Syringes Due to Sterility Concerns
Nephron Sterile Compounding Center is recalling 3,740 HYDROmorphone injection syringes due to lack of assurance of sterility. The affected lot was distributed nationwide.
Product
HYDROmorphone HCl Injection, USP, 50 mg/50 mL (1 mg/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. Extension, West Columbia, SC 29172, NDC: 69374-559-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1446-2022·2022-07-27
Cervical spinal implant connectors may have insufficient clamping force
Aesculap S4 Cervical Cross Connectors used in spinal fusion surgery may have insufficient clamping force, potentially causing movement of the connectors on the rods or wear debris.
Product
AESCULAP S4 Cervical Cross Connector L 28-33mm, S4C CROSS CONNECTOR VARIABLE 28-33MM, SW115T. Used in spinal fusion surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1387-2022·2022-07-27
SX-One MicroKnife Recalled for Potential Dull Blade Defect
Sonex Health LLC is recalling approximately 3,752 SX-One MicroKnife surgical instruments nationwide due to potential blade dulling that may compromise proper function.
Product
SX-One MicroKnife
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1253-2022·2022-07-27
Glycopyrrolate Injection Recalled for Lack of Sterility Assurance
Nephron is recalling Glycopyrrolate Injection pre-filled syringes distributed nationwide due to lack of sterility assurance. The recall affects 3,690 syringes from lot GL2001A, expiration 7/15/2022.
Product
Glycopyrrolate Injection, USP, 1 mg/5 mL (0.2 mg/mL) syringes, packaged in 5 x 5 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: 69374-903-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1261-2022·2022-07-27
Ketamine HCl Injection Recalled for Lack of Sterility Assurance
Nephron is recalling 47,905 pre-filled syringes of Ketamine HCl Injection nationwide due to lack of sterility assurance. Users should contact the manufacturer for handling instructions.
Product
Ketamine HCl Injection, USP, 50 mg/1 mL (50 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: 69374-511-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1467-2022·2022-07-27
QBee Honeycomb Toffee Dark Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling QBee Honeycomb Toffee Dark due to undeclared tree nuts. The product may contain pecans, almonds, coconut, macadamia nuts, or walnuts.
Product
QBee Honeycomb Toffee Dark. Net wt. 1.5 oz. PLU Code: 788394 10504 3.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1440-2022·2022-07-27
Nexiva Infusion Device Stopcock May Leak During Treatment
Becton Dickinson is recalling Nexiva infusion devices with pink stopcock components due to potential leakage at the housing that could interrupt treatment or expose patients to infusate and biohazardous material.
Product
Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1396-2022·2022-07-27
Surgical Seal Packaging May Compromise Sterility in Laparoscopic Devices
Surgical Innovations Ltd recalls YelloPort Elite Universal Seals due to potential holes in packaging that may affect product sterility. Worldwide distribution affected.
Product
YelloPort Elite Universal Seal. For use in laparoscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1458-2022·2022-07-27
Fudge Classic Truffle recalled for undeclared tree nuts
Queen Bee Gardens is recalling Fudge Classic Truffle candy because it may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Consumers with tree nut allergies should not consume this product.
Product
Fudge Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11045 0. Ingredients: Dark chocolate, milk chocolate, honey, butter (pasteurized cream & salt), cream, non-fat dry milk, whey, agar, algin, lecithin & natural flavors.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1431-2022·2022-07-27
BD Connecta Infusion Stopcock Recall Due to Potential Housing Leakage
BD Connecta Stopcock infusion devices may leak at the housing component, potentially delaying or interrupting treatment and exposing patients to biohazardous material. The recall affects 485,000 units distributed worldwide.
Product
BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1447-2022·2022-07-27
Aesculap S4 Cervical Cross Connector Recalled Due to Clamping Force Defect
Aesculap Implant Systems is recalling the S4 Cervical Cross Connector L 33-42mm due to insufficient clamping force that may cause connector movement or microparticle abrasion in spinal fusion implants.
Product
AESCULAP S4 Cervical Cross Connector L 33-42mm, S4C CROSS CONNECTOR VARIABLE 33-42MM, product code SW116T. Used in spinal fusion surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1473-2022·2022-07-27
Honey Caramels Butterscotch Recalled for Undeclared Tree Nuts
Queen Bee Gardens is recalling Honey Caramels Butterscotch due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Consumers with tree nut allergies should not consume this product.
Product
Honey Caramels Butterscotch. Net wt. 5.87 oz. PLU Code: 788394 12675 8. Ingredients: Honey, Butter (Pasteurized Cream & Salt), Cream, Grade A Non-Fat Dry Milk, Whey, Natural Flavors, Agar, Algin and Lecithin.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1269-2022·2022-07-27
FDA Recalls Nephron Cardioplegia Solution Over Sterility Assurance Concerns
Nephron Sterile Compounding Center is recalling del Nido Cardioplegia Solution due to lack of assurance of sterility. The 1765 bags affected were distributed nationwide.
Product
del Nido Cardioplegia Solution 1000 mL (1000 mL) Single-Dose Container IV bag, 4 x 1 IV Bag per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-984-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1275-2022·2022-07-27
Phenylephrine HCl injection recalled for lack of sterility assurance
Nephron Sterile Compounding Center recalls Phenylephrine HCl Injection syringes nationwide due to lack of sterility assurance. Patients with affected lots should contact their healthcare provider.
Product
Phenylephrine HCl Injection, USP, 0.8 mg/10 mL (80 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: 69374-956-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1280-2022·2022-07-27
Anticoagulant Sodium Citrate Solution Recalled for Sterility Assurance Failure
Nephron Sterile Compounding Center is recalling 85,300 pre-filled syringes of Anticoagulant Sodium Citrate Solution due to failure to assure sterility. Affected patients should contact their healthcare provider.
Product
Anticoagulant Sodium Citrate Solution, USP 4%, 200 mg/5 mL (40 mg/mL) syringe, packaged in 5 x 5 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: 69374-906-05
Category
Drug
Distribution
Distributed nationwide