127 “The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.” Ya think?! (www.fda.gov) posted 3 years ago by Eph612 3 years ago by Eph612 +127 / -0 19 comments share 19 comments share save hide report block hide replies
If I had it it was 3 weeks before covid was announced. It was a malaise and I never stopped.