Recalls629in this period
Food171FDA + USDA
Drugs117FDA
Class I170most serious
Class I 170 27%Class II 434 69%Class III 23 4%Other/pending 2
Recalls in October 2025, newest first
629 total
| Reported | Class | Recall | Company | Reason | Where |
|---|
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW Canon Ready, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | 266122 Salem Sump" Stomach Tube, Dual Lumen recalled | Cardinal Health 200 | Sterility | Nationwide |
| Device | CLASS III | One Step Sterile Lancet for Single Use (3 sizes) recalled | Home Health US, Incorporated | Sterility | Nationwide |
| Device | CLASS II | HeartSine Pad-Pak recalled by HeartSine Technologies | HeartSine Technologies | Other | Nationwide |
| Device | CLASS II | BD Phoenix M50 Instrument, labeled as the following recalled | Becton Dickinson & | Other | Nationwide |
| Device | CLASS II | Optima NX; dual-head nuclear medicine gamma camera designed recalled | Ge Medical Systems Israel, Functional Imaging | Lead & Heavy Metals | |
| Device | CLASS II | Model SM-32HF-Batt; 32KW Analog, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | Model Number SM-40HF-B-d-c; 40KW70CDEMO.005, Mobile X-ray system recalled | Sedecal | Other | CA, IL, NJ |
| Device | CLASS II | BD MAX System, for in vitro diagnostic (IVD) use recalled | Becton Dickinson & | Other | Nationwide |
| Device | CLASS II | Model Number 40KWFX, Mobile X-ray system recalled by Sedecal | Sedecal | Other | CA, IL, NJ |