State
73,096 recalls have nationwide distribution and so reach South Dakota. 2,684 additional recalls listed South Dakota specifically in their distribution scope.
Of the 2,684 recalls naming South Dakota we have scored against our rubric, 401 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 567 (21%) are Severe.
Which agencies issued them
These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline procedure kits containing defective plastic syringes are being recalled nationwide. The syringes may leak, break, or have other quality issues that could pose a risk to patient health.
Palmer & Company is recalling Snackin' With The Crew! Tiger Treats for potential salmonella contamination. The recalled products have best-by dates of 12/18/24 and 12/19/24 and were distributed nationwide in the U.S. and Canada.
Palmer & Company is recalling Palmer Patriotic Munchy Medley candy nationwide in the United States and Canada due to potential salmonella contamination.
Palmer & Company is recalling Palmer Candy Cookies & Cream Yummy Chow (Item 10706) nationwide due to potential salmonella contamination. Consumers should not consume the product.
Medline procedure kits containing defective plastic syringes have been recalled due to leaks, breakage, and quality issues that may harm patients. The recall affects over 1.6 million units distributed worldwide.
Palmer & Company is recalling multiple yogurt-covered pretzel products distributed nationwide due to potential salmonella contamination. Consumers should not consume these products.
Palmer & Company is recalling Urge! Caramel Swirl Pretzels and Casey's Caramel Swirl Coated Pretzels nationwide due to potential Salmonella contamination.
Palmer & Company is recalling Palmer Candy Vanilla Chocolatey Swirl Enrobed Pretzel Rods (8 oz) nationwide due to potential Salmonella contamination. Consumers should not consume this product.
Palmer & Company is recalling multiple Munchy Medley candy and snack products nationwide due to potential salmonella contamination. Salmonella can cause serious illness in vulnerable populations.
Al'Fez Natural Tahini in 5.6oz glass jars is being recalled due to potential Salmonella contamination. The recall affects 3,522 cases distributed nationwide.
Siemens recalled 24 units of the Luminos dRF Max X-ray display system because the support arm may unintentionally lower, potentially injuring personnel positioned beneath the equipment.
BD PYXIS automated medication dispensing cabinets contain a software issue that may print incorrect bin locations on restock labels. This could result in medications being placed in the wrong bin during restocking.
Steris Corporation recalls certain automated endoscope reprocessor hookups due to incorrect instructions in product documentation. Improper hookup connection could prevent proper endoscope disinfection, risking patient infection.
Baxter Healthcare Corporation is recalling the PST 500 U Precision Surgical Table due to loose spring pins that can cause the tabletop to unexpectedly tilt or move, potentially causing unintended patient movement during surgery.
Olympus is recalling Everest Bipolar Cutting Forceps surgical instruments due to fractures and breakages in packaging trays and Tyvek covers that may compromise sterility. Affected batches: FR150448, FR154445, FR173022.
Steris Corporation recalls 129 Hookup devices (Model 2-8-540HAN) due to incorrect hookup instructions in product documentation. Using wrong connections may prevent proper endoscope disinfection, creating infection risk.
Siemens LUMINOS Lotus Max X-ray displays are being recalled because the support arm may lower unintentionally, potentially injuring people nearby during positioning.
American Contract Systems is recalling Spine Pack convenience kits (Lot 980241) due to incomplete post-sterilization aeration. The affected kits were distributed in California, Kansas, Maine, Minnesota, Missouri, Nebraska, and South Dakota.
Artivion is recalling two CryoValve SG heart valve grafts that were approved and implanted with invalid test results.
Philips IntelliVue Patient Monitor models with software L.x and M.x lack critical monitoring capabilities due to a software update. This could result in incorrect or delayed patient treatment.
Steris Hookup Model 2-8-540 instructions were incorrectly documented, potentially preventing proper endoscope disinfection and risking patient infection.
Empower Pharmacy is recalling Estradiol Cypionate Injection due to lack of assurance of sterility. The recall affects 2,797 units distributed nationwide within the United States.
CareFusion is recalling 232 automated medication dispensing cabinets due to a software issue that may print incorrect medication bin labels, potentially causing medication dispensing errors.
CareFusion's BD PYXIS MEDBANK automated dispensing cabinet contains a software flaw that may print incorrect medication bin labels, potentially leading to dispensing of wrong medications.
A software error in CareFusion's BD PYXIS automated medication dispensing cabinet can cause incorrect medication bin numbers to be printed on restock labels, risking medication dispensing errors.