State
73,833 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.
Of the 8,501 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,204 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ossur H / F is recalling Lil Angel Vest P2 Lambswool units because the plastic stabilizer strap may partially or completely fracture.
Ossur H / F is recalling 435 Lil Angel Vest P2 Kodel units due to a potential for partial or complete fracture of the plastic stabilizer strap.
Philips Medical Systems is recalling the AutoSPECT Pro software application because it may incorrectly reconstruct cardiac SPECT data acquired with non-standard detector angles.
Siemens is recalling 1,096 SOMATOM Definition AS CT systems due to software bugs that may cause scan aborts, rescans, or accidental radiation.
Philips Medical Systems is recalling the AutoSPECT Pro software application because it may produce erroneous results when processing cardiac SPECT data acquired at detector angles other than 90 or 180 degrees.
Hale Products Inc. is recalling Class 1 Es-Key power control modules that may cause electrical short circuits, potentially leading to component damage or fire.
Spacelabs Healthcare is recalling Xhibit Telemetry Receivers due to frequent signal loss that may cause offline errors on central monitors.
Ossur H / F is recalling Lil Angel Vest P3 Lambswool units because the plastic stabilizer strap may fracture. The recall covers 435 units distributed in the US and Hong Kong.
Leica Microsystems is recalling 381 M525 and M720 surgical microscopes because an electronic component may overheat, causing smoke and smell.
Coloplast is voluntarily recalling a single lot of Self-Cath Pediatric Catheters because some units have missing eyelets, which can cause catheter malfunction.
Mako Surgical Corporation is recalling 249 Robotic Arm Interactive Orthopedic System (RIO) units worldwide to revise the field manual.
Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.
Materne North America Corp is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.
Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.
Stryker Neurovascular is recalling GDC 360 Detachable Coils because an incorrect Device Form Unique (DFU) was packaged with two lots.
Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.
Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.
Centro Naturista is recalling Smart Lipo dietary supplements due to multiple regulatory violations. Consumers should stop using the product.
Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.
Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.
Synthes (USA) Products LLC is voluntarily recalling specific lots of cervical spine screws because two different screw types were swapped during manufacturing.
Materne North America Corp. is voluntarily recalling specific GoGo squeeZ apple sauce pouches due to potential adulteration from food product residue.
Materne North America Corp. is voluntarily recalling specific GoGo squeeZ applesauce pouches due to potential adulteration from food product residue.
Optovue is recalling iVue and iVue 500 OCT systems due to a software anomaly that may display duplicate eye images instead of distinct right and left views.
Hospira is recalling 11,256 bags of Dextrose Injection, USP, 70% due to potential contamination with an aromatic hydrocarbon resin.