State
73,509 recalls have nationwide distribution and so reach Arkansas. 5,543 additional recalls listed Arkansas specifically in their distribution scope.
Of the 5,543 recalls naming Arkansas we have scored against our rubric, 1,029 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,446 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
ZOLL Circulation recalls Cool Line (Heparin) IVTM catheter kits due to potential leaks in catheter or start-up kit tubing. The recall affects 144 bundles distributed worldwide.
Paltop Advanced Dental Solutions is recalling Scan Abutment SP devices due to manufacturing tolerance deviations that may delay dental restoration. Affected devices showed orientation misalignment and size engraving errors.
FDA recalls Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit due to incorrectly labeled calibrator vials in Lot 00681Y600. The labeling error prevents the instrument from completing calibration successfully.
Exactech OPTETRAK Comprehensive Knee System inserts were packaged in vacuum bags lacking an additional oxygen barrier layer, which could allow material degradation. The recall affects 2,774 devices distributed worldwide.
ZOLL is updating labeling for ICY Intravascular Heat Exchange Catheter Kits due to potential leaks in the catheter or tubing. Healthcare providers should review updated guidance from the manufacturer.
Beckman Coulter is recalling 293,640 Access hsTnI High Sensitivity Troponin I reagent packs due to sample carryover contamination occurring with very high concentration samples, potentially affecting test accuracy.
Exactech is recalling approximately 242,397 OPTETRAK Comprehensive Knee System tibial components due to inadequate oxygen barrier in vacuum bag packaging. No injuries have been reported.
CardioQuip is recalling 1,646 units of its Modular Cooler-Heater 1000(m) due to inadequate labeling. The device documentation lacks guidance on proper water-quality maintenance and inspection procedures required for safe operation.
CardioQuip is recalling its Modular Cooler-Heater device because labeling omits proper guidance for water-quality maintenance and device inspection, affecting users' ability to maintain the device correctly.
ZOLL Circulation is updating labeling for its ICY Intravascular Heat Exchange Catheter Kit due to potential leaks in the catheter or start-up kit tubing. The recall affects 1,256 units distributed worldwide.
Paltop Advanced Dental Solutions is recalling Scan Abutment PCA devices due to manufacturing tolerance deviations that may delay implant restoration. Some devices show up to 2-degree orientation variance and sizing discrepancies.
Exactech, Inc. is recalling 41 custom OPTETRAK knee implant inserts due to packaging defects. The inserts were packaged in vacuum bags lacking adequate oxygen barrier protection.
Paltop Advanced Dental Solutions is recalling Scan Abutment SU devices (Catalog No. 30-70104) manufactured before July 21, 2021, due to manufacturing tolerance deviations that may delay dental restoration.
Paltop Scan Abutment WP dental implant scanning devices are recalled due to manufacturing defects. Affected units show dimensional tolerance deviations and size marking incongruences that may delay restoration procedures.
Paltop Advanced Dental Solutions is recalling Scan Abutment NP dental implant components due to manufacturing tolerance deviations that may affect implant restoration fit and timing.
ZOLL Circulation, Inc. is updating labeling for SOLEX 7 intravascular heat exchange catheter kits to communicate about potential leaks from the catheter or start-up kit tubing. The update affects 5,345 kits with worldwide distribution.
KTM North America is recalling specific 2018-2020 KTM and Husqvarna motorcycles because a damaged gasket on the clutch slave cylinder may prevent the clutch from disengaging, increasing crash risk.
Tilting Motor Works is recalling TRiO Conversion Kits because a bolt may fail, causing loss of traction power and increasing crash risk.
HME is recalling one 2014 Ford F-550 emergency vehicle because the dashboard may fail to warn drivers of emissions system faults, potentially causing loss of power.
Winnebago is recalling 2019-2022 Travato and 2021-2022 Boldt RVs. A faulty wire harness may lose over-current protection, causing wires to overheat and increasing fire risk. Owners must not drive until the Volta Power System is disabled.
Mercedes-Benz is recalling 2021 S 500 and S 580 vehicles because a software defect may deactivate the front passenger air bag, increasing injury risk in a crash.
HME is recalling 245 fire trucks from 2017-2020 because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.
Foretravel is recalling 2020-2022 iH-45, Realm, and iC-37 recreational vehicles because window adhesive may fail, causing the vent to detach and increasing crash risk.
Forest River is recalling 2021-2022 Entrada motorhomes because brake lines may wear against leveling jack brackets, potentially causing brake failure and increasing crash risk.
Forest River is recalling 2012-2016 Starcraft transit buses because rear emergency exit window labels are misplaced and incomplete, potentially delaying evacuation.