Recall BriefClass I
FDA Class I Recall: Nova StatStrip Gen 2.0 May Assign Results to the Wrong Patient
Nova Biomedical Corporation
Sourced Recall Intelligence
Device Recalls
Decision-oriented medical device recall briefs and selected FDA recall watch reports.
Recall BriefClass I
Philips Lumify Class I Recall Addresses Loss of Scanning
Philips Ultrasound, LLC
Recall BriefClass I
FDA Expands BD Alaris Pump Infusion Set Class I Recall
BD SWITZERLAND SARL (Z-3080-2026); CareFusion 303, Inc. (linked earlier actions)
Recall BriefType I
Health Canada Classifies Philips Lumify Ultrasound Recall as Type I
Philips Ultrasound Llc
Recall WatchClass II
FDA Class II Recall Watch: 28 September–4 October 2026
8 selected entries
Recall BriefType I
Recall BriefClass I
Recall WatchClass II
FDA Class II Recall Watch: 20–26 September 2026
8 selected entries
Recall BriefClass I
FDA Classifies Boston Scientific Imager II Catheter Recall as Class I
Boston Scientific Corporation
Recall BriefClass I
Recall BriefClass I
FDA Classifies BD Dialysis Convenience Kit Correction as Class I
Bard Access Systems, Inc.
Recall BriefClass I
Recall BriefClass I
FDA Classifies CooperSurgical INCA Infant Nasal CPAP Recall as Class I
CooperSurgical, Inc.
Recall WatchClass II
FDA Class II Recall Watch: 14–19 September 2026
8 selected entries
Recall BriefClass I
Recall BriefClass I
FDA Classifies Medical Action Epidural Kit Correction as Class I
Medical Action Industries, Inc. 306
Recall WatchClass II
FDA Class II Recall Watch: 30 August–5 September 2026
8 selected entries
Recall BriefClass I
FDA Classifies Boston Scientific Infinion CX Lead Removal as Class I Recall
Boston Scientific Neuromodulation Corporation
Recall WatchClass II
FDA Class II Recall Watch: 23–29 August 2026
8 selected entries
Recall BriefClass I
FDA Classifies AVID Medical Convenience Kit Correction as Class I
AVID Medical, Inc.
Recall BriefClass I
FDA Classifies Boston Scientific ENROUTE Transcarotid Neuroprotection System Recall as Class I
Boston Scientific Corporation
Recall WatchClass II
FDA Class II Recall Watch: 16–22 August 2026
8 selected entries
Recall BriefClass I
FDA Classifies Medline Convenience Kit Recall as Class I
Medline Industries, LP
Recall BriefClass I
FDA Classifies BD Intraosseous Needle Set Recall as Class I
Bard Access Systems, Inc.
Recall WatchClass II
FDA Class II Recall Watch: 9–15 August 2026
8 selected entries