Great! This is the graph for the Philips CPAP machines which had a big scandal associated with them and which likely got approved through various 510ks.

https://www.nytimes.com/2023/09/07/health/cpap-defect-recall...

One nitpick about the way that 510k.fyi presents this. A 'recall' in FDA lingo doesn't mean that the manufacturer withdrew the device from the market. It just means that they informed customers that there is something wrong with the device which requires any kind of modification by the manufacturer. It is thus a little bit ambiguous to say that a device was recalled if all this might mean that there was some software update which had to be applied.