State
73,806 recalls have nationwide distribution and so reach South Carolina. 7,153 additional recalls listed South Carolina specifically in their distribution scope.
Of the 7,153 recalls naming South Carolina we have scored against our rubric, 1,275 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,170 (30%) are Severe.
Which agencies issued them
These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
DePuy Mitek is recalling 401 Mitek Screw and Washer Depth Gauges because a design offset causes readings to be approximately 3.2mm shorter than the actual bone hole length.
CFMOTO is recalling approximately 1,800 2018 ZFORCE recreational off-highway vehicles because the throttle pedal may fail to return to idle, posing a crash risk.
Custom Healthcare Systems is recalling 40 units of CHS Custom Convenience Kit-INJECTION TRAY because incorrect sealing specifications compromised product sterility.
Howmedica Osteonics Corp. is recalling 58 units of the Tritanium TL Steerable Inserter because the locking mechanism may fail to function as intended due to lack of lubrication.
Custom Healthcare Systems is recalling 24 units of Penrose Drain Convenience Kits because incorrect sealing specifications compromised product sterility.
Siemens Healthcare Diagnostics is recalling StreamLab Refrigerated Storage Module 9000 units because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Custom Healthcare Systems is recalling 1,250 suture removal kits because incorrect sealing specifications compromised product sterility.
Custom Healthcare Systems is recalling 100 units of convenience kits because incorrect sealing specifications compromised product sterility.
Custom Healthcare Systems is recalling 630 CHS Custom Convenience Kits because incorrect sealing specifications compromised product sterility.
Siemens Healthcare Diagnostics is recalling 441 APTIO 15000 Refrigerated Storage Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Custom Healthcare Systems is recalling vaginal speculums because incorrect sealing specifications compromised product sterility.
Siemens Healthcare Diagnostics is recalling 186 StreamLab Automation Modules because they may have been shipped without a warning label regarding potential interference with pacemaker functionality.
Custom Healthcare Systems is recalling 250 units of 22G LP Needle Convenience Kits because incorrect sealing specifications compromised product sterility.
Custom Healthcare Systems is recalling 80 units of Toenail Removal Kits because incorrect sealing specifications compromised product sterility.
Medtronic is recalling 596 O-arm 1000 2nd Edition Imaging Systems worldwide due to software anomalies affecting startup, communication, and imaging functions.
ESAOTE S.P.A. is recalling 10 MyLab Alpha Model 7400 ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Ecolab is recalling specific lots of Disposable Accessory Kits for the Da Vinci Si Robotic system because wrinkles in the packaging seal could compromise sterility.
Custom Healthcare Systems is recalling 7,200 surgical gown kits because incorrect sealing specifications compromised product sterility.
Custom Healthcare Systems is recalling 50 units of curved pean forceps kits because incorrect sealing specifications compromised product sterility.
Kia is recalling 2019 Forte vehicles with LED headlights because they may not be aimed correctly, potentially reducing driver visibility and increasing crash risk.
ESAOTE is recalling 10 MyLab Seven ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Custom Healthcare Systems is recalling 100 units of toothbrush kits because incorrect sealing specifications compromised product sterility.
Canon Medical System is recalling 252 MRI systems because the displayed SAR value may be lower than the actual value, potentially exceeding safety limits.
Custom Healthcare Systems is recalling 4,500 fenestrated drape kits because incorrect sealing specifications compromised product sterility.
Custom Healthcare Systems is recalling Webster Needle Holder Convenience Kits because incorrect sealing specifications compromised product sterility.