Medical device recalls
Device recalls are the largest single group in this archive, because the FDA logs corrections and removals as well as outright withdrawals. Many are handled entirely between the manufacturer and a hospital and need nothing from a patient. Each notice states who has to act.
13,634 stored notices, reported between Jun 20, 2012 and Sep 9, 2026. Newest first.
Reported May 6, 2026
Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Immuno-Mycologics, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Medline Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.25" X…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
37 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2026
Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment of atrial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2026
VACUUM BAG SU LARGE, Non-sterile specimen container, Model/Catalog Number: 68409SS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Milestone S.R.L.
FDA (openFDA device enforcement)
Reported May 6, 2026
AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits…
High riskUsing this product could cause serious injury, illness or death — stop using it now.North American Rescue LLC.
FDA (openFDA device enforcement)
Reported May 6, 2026
Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2. Model Number (REF): 781296.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
18 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2026
epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Dimension Creatinine Flex reagent cartridge. Material Number: 10872079.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 6, 2026
WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor battery-operated…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whill, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog No.: 10707103;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
19 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Access Total T4 Calibrator, Catalog No. 33805
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Davol, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator, 6mm-7mm-8mm, REF 1204-08
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diversatek Healthcare
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Foundation Medicine, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
FDA (openFDA device enforcement)
Reported Apr 29, 2026
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LSL Healthcare Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
(1)(2) LeadCare¿ II Blood Lead Test Kit, (3)LeadCare¿ II 5X Blood Lead Test Kit, (4)LeadCare¿ II 9X Blood Lead Test Kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Magellan Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM ANG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
38 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-X Ltd.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
15 more products in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.