101 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Recall
×
S4 and patient cable for the S4 Wireless Telemeter with the following device names: CABLE 10 WIRE LF ECG SNAP ENDS AHA GRAY, CABLE 10 WIRE LF ECG SNAP ENDS IEC GRAY, CBL 10WIRE LF LRG ECG SNAP ENDS AHA GRAY, CBL 10WIRE LF LRG ECG SNAP ENDS IEC GRAY. The S4 mobile monitor provides a means to acquire and transmit simultaneous ECG and SpO2 data to a Surveyor Central Station monitoring system while allowing the patient to be ambulatory within the range of the WiFi network.
FDA Recall
Terminated
·WELCH ALLYN, INC/MORTARA·Product code DPS·March 18, 2020
Vl DBL OFFST WI LRG STPL, RT Nonsterile
FDA Recall
Terminated
·Zimmer, Inc.·Product code LXH·July 23, 2014
VI DBL OFFST W/ LRG STPL, LT Nonsterile
FDA Recall
Terminated
·Zimmer, Inc.·Product code LXH·July 23, 2014
AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033
FDA Recall
Open, Classified
·Cardinal Health Inc.·Product code NVP·March 16, 2021
Depuy brand LCS Complete metal backed patella, cemented, LRG; REF 1294-09-760.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005
Depuy brand LCS Complete metal backed patella, porocoat, LRG+; REF 1294-09-670.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005
Depuy brand LCS Complete metal backed patella, porocoat, LRG; REF 1294-09-660.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005
Depuy brand LCS Complete metal backed patella, cemented, LRG+; REF 1294-09-770.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code NJL·June 7, 2005
INTERLOCKING IM SCREW SML, MED and LRG; M/DN TIBIAL I/M NAIL 6 MM to 15 MM. Some items starting with codes 0022530, 0022531, 002532, 0022533, 0022534
FDA Recall
Terminated
·Zimmer, Inc.·Product code HSB·October 11, 2013
The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
FDA Recall
Open, Classified
·BigTree Sales Inc.·Product code RHP·August 29, 2025
Ossur OB Resolve, Sterile, Part/ Description: 505300D/ OB RESOLVE STERILE RING SML; 505400D/ OB RESOLVE RING KIT STD; 505500D/ OB RESOLVE RING KIT LRG; 515300D/ OB RESOLVE RING KIT SM-No App; 515400D/ OB RESOLVE RING KIT STD-No App; 515500D/ OB RESOLVE RING KIT LG-No App; 540D/ OB RESOLVE COMPONENT TRAY
FDA Recall
Terminated
·Ossur Americas·Product code HAX·June 21, 2018
MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus instrument access door hinge. Siemens Healthcare Diagnostics, Inc. in vitro diagnostic
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code LRG·June 2, 2014
MicroScan WalkAway-40 plus Instrument REF B1018-283
FDA Recall
Open, Classified
·Beckman Coulter Inc.·Product code LRG·October 21, 2019
MicroScan WalkAway-96 plus Reconditioned Instrument REF B1018-396R
FDA Recall
Open, Classified
·Beckman Coulter Inc.·Product code LRG·October 21, 2019
MicroScan Pos MIC Panel Type 34 - Product Usage: For the determination of antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some fastidious aerobic cocci and listeria monocytogenes.
FDA Recall
Terminated
·Beckman Coulter Inc.·Product code LRG·December 2, 2020
MicroScan WalkAway-96 plus Reconditioned Instrument
FDA Recall
Terminated
·Beckman Coulter Inc.·Product code LRG·September 4, 2019
MicroScan WalkAway-40 plus Instrument
FDA Recall
Terminated
·Beckman Coulter Inc.·Product code LRG·September 4, 2019
MicroScan WalkAway-96 plus Instrument REF B1018-284
FDA Recall
Open, Classified
·Beckman Coulter Inc.·Product code LRG·October 21, 2019
DxM 1040 MicroScan WalkAway Instrument REF B1018-440
FDA Recall
Open, Classified
·Beckman Coulter Inc.·Product code LRG·October 21, 2019
MicroScan WalkAway-96 plus Instrument
FDA Recall
Terminated
·Beckman Coulter Inc.·Product code LRG·September 4, 2019