8 results
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12ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
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Penner Pacific Bathing Spa, Model Numbers 360020-1EP
FDA Recall
Open, Classified
·Penner Patient Care, Inc.·Product code ILJ·August 13, 2025
Medline Kits: 1) SYR CNTRL 10ML RING W/ROT NB, Model Number: DYNJSYR10CWRB; 2) MANIFOLD KIT LOW PRESSURE OFF, Model Number: VASCSLPOFF1; 3) EP MANIFOLD KIT, Model Number: VASC1018A
FDA Recall
Open, Classified
·Product code DXT·February 25, 2026
Medline Convenience kits labeled as: 1) EP DRAPE PACK-LF, Pack Number DYNJ0209716K ; 2) MERCY COMBINED PACK-LF, Pack Number DYNJ0233004D ; 3) E P DRAPE PACK-LF , Pack Number DYNJ0373061J ; 4) PACEMAKER DRAPE PACK-LF , Pack Number DYNJ0406118K ; 5) FEMORAL ANGIOGRAPHY PACK, Pack Number DYNJ0618509F ; 6) EP DRAPE PACK-LF, Pack Number DYNJ22911I ; 7) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ36314J ; 8) SPLIT DRAPE , Pack Number DYNJ37265F ; 9) 4 DRAPE PROCEDURE PACK, Pack Number DYNJ39689D ; 10) DR MOTT DRAPE PACK, Pack Number DYNJ42065B ; 11) PK, EP LAB, Pack Number DYNJ43815C ; 12) MAYO STAND PACK , Pack Number DYNJ50738; 13) DAA BI-LAT, Pack Number DYNJ903538C; 14) PACEMAKER , Pack Number DYNJ903545C; 15) CSTM NEONATAL FEM DRAPE PK, Pack Number DYNJCD0114
FDA Recall
Open, Classified
·MEDLINE INDUSTRIES, LP Northfield·Product code KKX·April 8, 2024
Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Whole Blood Microcoagulation System
FDA Recall
Open, Classified
·Accriva Diagnostics, Inc.·Product code JBP·November 5, 2025
VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198
FDA Recall
Open, Classified
·Ortho-Clinical Diagnostics, Inc·Product code CEP·March 25, 2022
VIDAS LH, REF 30406-01
FDA Recall
Open, Classified
·bioMerieux, Inc.·Product code CEP·September 22, 2021
Medtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03
FDA Recall
Open, Classified
·Medtronic Perfusion Systems·Product code JBP·October 20, 2025
VIDAS CLINICAL VIDAS LH 60 TESTS, CATALOG 30406-01
FDA Recall
Open, Classified
·Biomerieux Inc·Product code CEP·November 9, 2022