78 results
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13ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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Product Desc: Product Name: A-OK SATINCRESCENT FULL HANDLE2.3MM ANG Model/Catalog Number: 8065990002 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
FDA Recall
Open, Classified
·Alcon Research LLC Aspex Facility·Product code HNN·July 15, 2024
Product Desc: Product Name: A-OK SATINSLIT FULL HANDLE2.75MM ANG SG Model/Catalog Number: 8065992761 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
FDA Recall
Open, Classified
·Alcon Research LLC Aspex Facility·Product code HNN·July 15, 2024
Product Desc: Product Name: A-OK 19G V-LANCE FULL HANDLE1.6MM SATIN Model/Catalog Number: 8065911901 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
FDA Recall
Open, Classified
·Alcon Research LLC Aspex Facility·Product code HNN·July 15, 2024
Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code PHC·June 20, 2025
Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2
FDA Recall
Open, Classified
·Baxter Healthcare Corporation·Product code PHC·June 20, 2025
Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET US CT900B PROG CT900B CLINICIAN TABLET EU -UK CT900C PROG CT900C CLINICIAN TABLET UK CT900D PROG CT900D CLINICIAN TABLET GLOBAL CT900E PROG CT900E CLINICIAN TABLET GLBL SMSNG CT900F PROG CT900F CLINICIAN TABLET GLBL SMSNG
FDA Recall
Open, Classified
·Medtronic Neuromodulation·Product code LGW·November 20, 2025
Lunar iDXA bone densitometer
FDA Recall
Open, Classified
·GE Healthcare, LLC·Product code KGI·December 3, 2019
Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer
FDA Recall
Open, Classified
·GE Healthcare, LLC·Product code KGI·December 3, 2019
Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer
FDA Recall
Open, Classified
·GE Healthcare, LLC·Product code KGI·December 3, 2019
Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer
FDA Recall
Open, Classified
·GE Healthcare, LLC·Product code KGI·December 3, 2019
Alinity ci-series System Control Module clinical chemistry and immunoassay analyzer for in vitro diagnostic use. Model number LN 03R70-01
FDA Recall
Open, Classified
·Abbott Laboratories·Product code JJE·July 26, 2021
Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens for Mycobacterium spp. diagnosis
FDA Recall
Open, Classified
·Immuno-Mycologics, Inc·Product code PPM·March 26, 2026
Candida ID Antigen, REAG, AG, REF C50110, Vol 1 mL REF ID1001, Immy Fungal Antigens, Positive Controls, & Immunodiffusion (ID) plates for use in the ID test, RX only, IVD, CE
FDA Recall
Open, Classified
·Immuno-Mycologics, Inc·Product code GMI·February 10, 2025
ROTATION MEDICAL TENDON STAPLES (8) (narrow indication)-Intended for fixation of prosthetic material to soft tissues. Product Number: 72205201
FDA Recall
Open, Classified
·Smith & Nephew Inc.·Product code GDW·August 12, 2024
ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation of prosthetic material to soft tissues. Product Number: 2504-1
FDA Recall
Open, Classified
·Smith & Nephew Inc.·Product code GDW·August 12, 2024
20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
FDA Recall
Open, Classified
·Alcon Research LLC Aspex Facility·Product code HNN·April 22, 2024
ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
FDA Recall
Open, Classified
·Alcon Research LLC Aspex Facility·Product code HNN·April 22, 2024
ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
FDA Recall
Open, Classified
·Alcon Research LLC Aspex Facility·Product code HNN·April 22, 2024
ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
FDA Recall
Open, Classified
·Alcon Research LLC Aspex Facility·Product code HNN·April 22, 2024
t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM, and t:slim X2 Insulin Pump with Basal-IQ Technology
FDA Recall
Open, Classified
·Tandem Diabetes Care Inc·Product code PQF·September 10, 2020