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(255)
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(818)
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(217)
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(17)
Surgical Equipment
(896)
896 recalls
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Medtronic Xomed
Medium Risk
FDA Device
Medtronic Xomed, Inc.: Medtronic ENT Ultra Round Steel Cutting Bur Recalled for Past Expiration Date
Recalled
Sep 12, 2024
Added
Mar 21, 2026
B Braun Medical
Medium Risk
FDA Device
Introcan Safety 3 Closed IV Catheters Recalled for Valve Detachment Risk
Sold in 16 states
Sold at hospitals, medical supply distributors
28,200 units affected
Recalled
Mar 19, 2025
Added
Mar 21, 2026
Spectrum Medical
Medium Risk
FDA Device
Spectrum Medical Quantum Perfusion Blood Pump Recalled for Fluid Leakage
Sold in 27 states
Sold at Spectrum Medical Inc
Recalled
Mar 13, 2025
Added
Mar 21, 2026
Maquet Medical Systems USA
Low Risk
FDA Device
CARDIOHELP-i Heart Lung Support System Recalled for Improper Leakage Testing
Distributed nationwide
Sold at Authorized medical distributors
Recalled
Sep 30, 2024
Added
Mar 21, 2026
WOM World Of Medicine AG
Medium Risk
FDA Device
WOM World Of Medicine AG: Irrigation Tube Sets Recalled for Incorrect RFID Data and Surgery Delays
Distributed nationwide
Sold at Endoscopy Smith & Nephew Inc.
Recalled
Jul 1, 2024
Added
Mar 21, 2026
Coloplast Manufacturing US
Medium Risk
FDA Device
Coloplast Manufacturing US, LLC: Ureteral Dilators Recalled for Potential Sterility Packaging Breach
Sold in 9 states
Sold at Medical facilities, Specialty healthcare distributors
Recalled
Apr 2, 2024
Added
Mar 21, 2026
Scientia Vascular
Medium Risk
FDA Device
Plato 17 Microcatheter Recalled for Potential Sterile Barrier Breach
Sold in Delaware
Sold at Specialized medical distributors
Recalled
Feb 26, 2025
Added
Mar 21, 2026
Medline Industries
Medium Risk
FDA Device
Medline Sterile Scissors and Forceps Recalled for Potential Sterility Breach
Sold in 5 states
Sold at Hospitals, Medical facilities +2 more
Recalled
Dec 12, 2025
Added
Mar 21, 2026
Maquet Cardiovascular
Medium Risk
FDA Device
Maquet VH-3010 Power Supply Recalled for Potential Heating Failure
Sold in 27 states
Sold at Authorized medical distributors
Recalled
Apr 16, 2025
Added
Mar 21, 2026
Bard Peripheral Vascular
Medium Risk
FDA Device
Bard Peripheral Vascular Inc: Marquee Disposable Core Biopsy Instrument Kits Recalled for Needle Mismatch
Sold in 17 states
Sold at Medical distributors, Direct to hospitals
Recalled
Oct 4, 2023
Added
Mar 21, 2026
Elekta Instrument AB
Critical Risk
FDA Device
Elekta Instrument AB: Disposable Biopsy Needle Kits Recalled for Internal Microscopic Debris
Distributed nationwide
Sold at Specialty medical distributors
Stainless steel fragments contamination
Recalled
Apr 16, 2024
Added
Mar 21, 2026
UNIMAX MEDICAL SYSTEMS
Medium Risk
FDA Device
Tech Medical, UNIMAX, and ConMed Endo Pouches Recalled for Detachment Risk
Sold in Georgia, Missouri, Pennsylvania
Sold at Tech Medical Services Inc., ConMed Corporation
81,241 units affected
Recalled
Sep 17, 2024
Added
Mar 21, 2026
MICROVENTION
Medium Risk
FDA Device
MicroVention ERIC Retrieval Devices Recalled for Incorrect Expiration Dates
Sold in 16 states
Sold at MicroVention Inc.
Recalled
Sep 17, 2024
Added
Mar 21, 2026
Maquet Cardiovascular
Medium Risk
FDA Device
Maquet Cardiovascular, LLC: Vasoview 6 Pro Recalled for Incorrect Packaging and Labeling
Sold in 13 states
Sold at Maquet Cardiovascular, LLC
Recalled
Nov 2, 2023
Added
Mar 21, 2026
Argon Medical Devices
High Risk
FDA Device
Argon BioPince and Tru-Core Biopsy Instruments Recalled for Infection Risk
Sold in 47 states
Sold at Authorized Medical Distributors, Hospitals +1 more
micro-organisms contamination
Recalled
Sep 20, 2024
Added
Mar 21, 2026
Applied Medical Technology
Medium Risk
FDA Device
Applied Medical Technology Inc: Devices were labelled with the incorrect guidewire labelling.
Recalled
Jun 28, 2024
Added
Mar 21, 2026
PREMIA SPINE
Medium Risk
FDA Device
TOPS Inserter Recalled for Potential Missing Pins
Sold in Connecticut
Sold at Medical distributors, Surgical centers
Recalled
Sep 4, 2025
Added
Mar 21, 2026
Beaver Visitec International
Medium Risk
FDA Device
Beaver Visitec International, Inc.: Crescent Knife Recalled Due to Incorrect Blade Orientation
Distributed nationwide
Sold at International medical distributors
Recalled
Jan 4, 2024
Added
Mar 21, 2026
Lutronic
Medium Risk
FDA Device
Lutronic XERF EFFECTOR 60 Electrosurgical Units Recalled for Defects
Sold in 8 states
Sold at Medical device distributors, Direct clinical sales
Recalled
Oct 14, 2025
Added
Mar 21, 2026
High Risk
FDA Device
Olympus Corporation of the Americas: ENDOEYE HD II Rigid Videoscopes Recalled for Image Coloration Issues
Distributed nationwide
Sold at Authorized Medical Distributors, Hospital Supply Chains
Potential for mucosal injury or bleeding; device exchange may result in prolonged surgery.
Recalled
Jan 10, 2024
Added
Mar 21, 2026
Medline Industries
Medium Risk
FDA Device
Medline DEXLOCK Achilles Repair Kits Recalled for Drill Bit Fusing Issue
Sold in 24 states
Sold at Medical Supply Distributors, Hospitals +1 more
Multiple complaints of drill bit fusing; surgical procedures prolonged.
Recalled
Dec 11, 2025
Added
Mar 21, 2026
Noah Medical
Medium Risk
FDA Device
Noah Medical Galaxy Bronchoscopic System Recalled for Potential Power Loss
Sold in 16 states
Sold at Authorized Medical Distributors
Recalled
Dec 18, 2024
Added
Mar 21, 2026
LUMENIS
Medium Risk
FDA Device
OtoLase Starter Kits Recalled for Potential Lack of Sterility
Sold in Pennsylvania, Wisconsin
Sold at Surgical distributors
potential microbial contamination contamination
Recalled
Aug 21, 2025
Added
Mar 21, 2026
LimFlow
Medium Risk
FDA Device
LimFlow Vector Devices Recalled for Incorrect Expiration Date
Sold in 15 states
Sold at Direct distribution to hospitals and clinics
Recalled
Jan 29, 2026
Added
Mar 21, 2026
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