State
73,597 recalls have nationwide distribution and so reach DC. 2,798 additional recalls listed District of Columbia specifically in their distribution scope.
Of the 2,798 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,083 (39%) are Severe.
Which agencies issued them
These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fujifilm is recalling Synapse PACS Software versions 5.1 and higher because it may display incorrect patient information or PET/CT values.
Abbott Point Of Care Inc. is recalling i-STAT EG7+ cartridges because the ionized calcium test may report higher than expected results if stored at room temperature for specific periods.
Boston Scientific is retrieving five ACUITY Universal Cutters that did not undergo the required sterile processing procedure.
Roche is recalling 76 licenses of Cobas Infinity software due to an error that may remove quality flags, allowing unreliable test results to be reported.
Skeletal Kinetics is recalling 2 units of OsteoVation Inject Bone Filler Kits because of a discrepancy between the Mixing Instruction Card and the Instructions for Use.
Complete Pharmacy and Medical Solutions is recalling 2,418 vials of Human Chorionic Gonadotropin because the product lacked required potency testing.
Beckman Coulter is recalling 276 units of ACCESS SARS-CoV-2 IgG Quality Control cards due to a label error regarding standard deviation values.
Skeletal Kinetics is recalling 49 units of OsteoVation bone filler kits because the mixing instructions on the card do not match the Instructions for Use.
Smiths Medical ASD Inc. is recalling 4,440 Portex Acapella DH Vibratory PEP Devices because shipping boxes may contain the wrong model number.
Complete Pharmacy and Medical Solutions is recalling 2,400 vials of Human Chorionic Gonadotropin 1,250 IU due to a lack of potency testing.
Piping Rock Health Products is recalling 296 jars of Fitness Labs Organic Coconut Oil due to potential mold contamination. The product was distributed in 34 states and Washington, D.C.
Allergan is recalling Refresh Relieva Preservative-Free eye drops because the packaging is missing the instructions for use insert.
Abbott is recalling i-STAT CG8+ cartridges because the ionized calcium test may report higher than expected results if stored at room temperature for specific periods.
Excellance is recalling 2019-2020 RAM 4500 and 5500 trucks modified with CLASS Suspension Systems because rear brake lines may wear, causing brake failure.
Subaru is recalling 2021 Outback and Impreza models due to an improperly tightened CVT select lever cable nut that may loosen, causing the gear selector to malfunction and increasing crash risk.
Nissan is recalling 2020 INFINITI QX50 vehicles because the tire and loading information placard may be illegible, potentially leading to incorrect tire installation or overloading.
Brembo is recalling specific brake pads that may corrode and detach, potentially increasing stopping distance and crash risk.
Keystone RV Company is recalling 2021 Dutchmen Voltage trailers because the Federal Identification Tag incorrectly lists tire pressure as 95 PSI instead of 110 PSI, which could cause underinflated tires and increase crash risk.
Keystone RV Company is recalling 2020–2021 Dutchmen Voltage recreational trailers because the Federal Identification Tag lists incorrect tire pressure (110 PSI instead of 95 PSI), which could cause tire overinflation and increase crash risk.
Fresenius Medical Care is recalling 176 drums of Citrasate Liquid Acid concentrate because sodium and/or calcium levels were below manufacturing specifications.
Keystone is recalling 2019-2020 Impact recreational trailers because a propane gas leak in the stove can increase the risk of fire.
Boston Scientific is recalling 302 Lotus Edge Valve Systems because a visual inspection error could prevent the delivery system from releasing during deployment.
Boston Scientific is recalling 386 Lotus Edge Valve Systems because a visual inspection error could prevent the delivery system from releasing during deployment.
Sunstar Americas is recalling Paroex Oral Rinse due to potential Burkholderia cepacia complex contamination and manufacturing facility violations.
Edge Pharma, LLC is recalling 71 syringes of Methotrexate USP Sterile Solution for Injection because the media used for post-compounding sterility testing was expired.