State
73,741 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.
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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cayenne Medical Inc. is recalling 976 units of AperFix AM Femoral Implants because they may break inside the femoral socket during orthopedic use.
Medtronic is recalling 103 EnTrust Dual Chamber ICDs because they may lose high voltage and anti-tachycardia pacing therapy near end-of-life without prior warning.
Medtronic is recalling 1,604 Percepta CRT-P MRI SureScan implantable pulse generators due to a potential device reset caused by a timing interaction between diagnostic and pacing features.
Arrow International is recalling 2,070 VPS Rhythm ECG Accessory Packs because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.
Anika Therapeutics is recalling Hyalomatrix wound dressings because PVC in the packaging degraded during sterilization, potentially compromising product integrity.
Teva Pharmaceuticals USA is recalling Fluocinolone Acetonide Topical Solution due to failed impurity and potency specifications.
Lupin Pharmaceuticals is recalling Nitrofurantoin Oral Suspension because the drug is subpotent and failed content uniformity testing.
Arrow International Inc. is recalling 2,070 units of VPS Rhythm ECG Accessory Packs because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.
Arrow International is recalling 2,070 Peripherally Inserted Midline Catheter Kits because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.
Ohio Medical Corporation is recalling 11 Vacuum Regulator units because final quality control testing was not completed before distribution.
Medgyn Products, Inc. is recalling 2,750 boxes of Monsel's Solution because the product was not manufactured under current good manufacturing practices.
Smiths Medical ASD Inc. is recalling 10 BCI Advisor Vital Signs Monitors because certain printing modes may not function properly.
bioMerieux is recalling 1,866 mini VIDAS systems because pump clogging and label displacement may cause erroneous test results.
Wockhardt Limited is recalling specific batches of Enalapril Maleate Tablets USP because they failed impurity and degradation specifications.
Sanofi-Aventis is recalling 3,214 Admelog insulin pens because they may not have been shipped at the proper temperature.
Arrow International Inc. is recalling 2,070 units of the VPS TipTracker Stylet Accessory because the product pouch label may not easily identify the lot number, expiration date, and associated symbols.
Mylan Pharmaceuticals is voluntarily recalling 28,436 bottles of Triamterene and Hydrochlorothiazide Tablets because the medication was found to be subpotent.
Wockhardt Limited is recalling specific batches of Enalapril Maleate Tablets USP because they failed impurity and degradation specifications.
Smithfield Packaged Meats is recalling approximately 24,048 pounds of pepperoni five cheese calzones that may contain hard, sharp, clear plastic pieces.
Martinrea is recalling brake hose assemblies for Chrysler and Ford vehicles that may lack anti-corrosion plating, posing a risk of brake fluid leaks and reduced braking effectiveness.
Hickory Springs is recalling specific school bus seats because the foam in the knee impact area may not absorb enough energy in a crash, increasing injury risk.
BMW is recalling 2018 M5 vehicles because a fuel level sensor may stick to a fuel line, causing inaccurate fuel gauge readings that could lead to stalling and increased crash risk.
Ford is recalling 2013-2016 Fusion and 2013-2014 Escape vehicles because a transmission shifter cable bushing may degrade, allowing the vehicle to move unexpectedly.
TRW is recalling brake caliper pistons with insufficient coating for vehicles from Volkswagen, Fiat Chrysler, BMW, and Mercedes-Benz to prevent reduced braking performance.
Ford is recalling 2018 F53 stripped chassis vehicles because improperly heat-treated front wheel studs may break, increasing crash risk.