State
73,827 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Health Matters America is recalling Organic Traditions Sprouted Flax Seed Powder due to potential Salmonella contamination. Consumers should stop using the product.
Mako Surgical Corporation is recalling 96 units of the RESTORIS PST RIO Offset Shell Impactor due to a potential disassociation of the orientation pin.
Research Instruments Ltd is recalling 380 Integra 3 micromanipulators because they were fitted with a potentially faulty power supply cable.
NOW Foods is recalling 57 bottles of Elderberry 500 mg capsules because they contain undeclared soy lecithin, a common allergen.
Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers due to malfunctions triggered by specific system alarms.
GE Medical Systems is recalling Aisys and Aisys CS2 anesthesia machines because kinked vacuum suction tubing may cause inadequate airway clearance and ventilation.
Becton Dickinson is recalling Trypticase Soy Agar and MacConkey II Agar plates contaminated with Listeria monocytogenes. The non-sterile media are used for growing and detecting bacteria.
Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers because they malfunction when specific alarms appear on the system.
Elekta is recalling 217 Radionuclide Radiation Therapy Systems because frame adapter latches can lock without proper pin insertion, potentially compromising treatment accuracy.
Auto Truck is recalling 2013-2016 IMT Dominator Series III vehicles because a valve bank cover may crack and fall off, creating a road hazard.
Siemens is recalling 37 SOMATOM Force CT systems because a software error in the Neonate Head protocol may cause image artifacts, potentially leading to misdiagnosis.
NOW Foods is recalling Gingko Biloba 60mg capsules because they contain undeclared soy lecithin. Consumers should stop using the product and return it to the place of purchase.
NOW Foods is recalling 3 bottles of cranberry extract capsules due to undeclared soy lecithin. The product was distributed to 499 consignees in the US and one in Japan.
Volvo is recalling 2016 XC90 vehicles because the sunroof switch may be unintentionally pressed, causing the panel to close and increasing the risk of occupant injury.
NOW Foods is recalling Andrographis extract 400 mg capsules due to undeclared soy lecithin. The product was distributed to 499 consignees in the US and one in Japan.
Roche Molecular Systems is recalling 6,939 IT3800 hand-held barcode scanners because they mis-identified sample barcodes when used with the COBAS AmpliPrep instrument.
Shimadzu Medical Systems is recalling 185 X-Ray Diagnostic Tables (Model YSF-300) due to reports of unintentional movement to reverse tilting.
Intuitive Surgical is recalling 43 EndoWrist Stapler instruments for the da Vinci Xi system due to a risk of unexpected jaw motion during use.
NOW Foods is recalling Goldenseal Root 500 mg capsules because they contain undeclared soy lecithin, a common allergen.
Stryker is recalling 143 Spirit One A-C Powered Hospital Beds because of customer complaints regarding a faulty brake system.
Stryker is recalling 143 Spirit One A-C Powered Hospital Beds because their scale systems are inaccurate. The beds were distributed in 19 US states, Canada, and the UK.
Corin USA Limited is recalling 629 Trinity Acetabular Shells used in total hip replacements because the new packaging system may abrade the sterile barrier pouches.
Liquid Coffee Inc is recalling 642 gallons of concentrated coffee because the pH level was elevated above 4.6. The product was distributed nationwide to specific states.
Family Dollar is recalling Family Gourmet Long Grain Enriched White Rice because live insects were found inside unopened bags.
Boston Scientific is recalling four Ultraflex Tracheobronchial stents because 10mm diameter units were mislabeled as 12mm diameter.