242 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Recall
×
GII QuickAnchor Plus, ETHIBOND Polyester Suture, 36", double-Armed w/CP 2 Needles 2. Ref. 212034 Lot 123266 General and Plastic Surgery
FDA Recall
Terminated
·Surgical Instrument Service And Savings, Inc.·Product code GAS·May 3, 2013
Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are absent or incompetent.
FDA Recall
Open, Classified
·Smith & Nephew, Inc.·Product code JWH·September 21, 2020
Patient tables of CT systems with brand name: CT/e; CT/e Dual; CT/e Plus, CT/e Dual Plus; CT/e Lite; ProSpeed AI; ProSpeed AII; ProSpeed FI; ProSpeed FII; ProSpeed EII; CT HiSpeed Series.
FDA Recall
Terminated
·General Electric Med Systems LLC·Product code IXR·October 21, 2004
MultiDiagnost MD4
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
LithoDiagnost
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
Diagnost 96/97 DSI
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
UroDiagnost
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
MultiDiagnost MD3
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
EasyDiagnost
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
Easy Diagnost Digital
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
OmniDiagnost
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
Diagnost 76
FDA Recall
Terminated
·Philips Medical Systems North America Co. Phillips·Product code JAA·July 6, 2009
PRN 50-M+, GE part number 2062759-001, manufacturer part number 600-23310-01 Product Usage: The PRN 50M+ Paper Chart Recorder thermally records patient data on a paper strip. This device is intended for use under direct supervision of a licensed health care practitioner. This device is not intended for home use.
FDA Recall
Terminated
·Gsi Group Inc·Product code DSF·December 2, 2015
18 Coated Super Tampons; Model Number: FG-TMP-REF00180000;
FDA Recall
Open, Classified
·DAYE (ANNE'S DAY LTD)
Biscuit Factory Business Complex
100 Drummond Road
London United Kingdom·Product code HEB·February 17, 2025
Initiation 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-IB09090909;
FDA Recall
Open, Classified
·DAYE (ANNE'S DAY LTD)
Biscuit Factory Business Complex
100 Drummond Road
London United Kingdom·Product code HEB·February 17, 2025
Refill 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-REF09090909;
FDA Recall
Open, Classified
·DAYE (ANNE'S DAY LTD)
Biscuit Factory Business Complex
100 Drummond Road
London United Kingdom·Product code HEB·February 17, 2025
18 Coated Regular Tampons; Model Number: FG-TMP-REF18000000;
FDA Recall
Open, Classified
·DAYE (ANNE'S DAY LTD)
Biscuit Factory Business Complex
100 Drummond Road
London United Kingdom·Product code HEB·February 17, 2025
Refill 36 Coated Regular Tampons; Model Number: FG-TMP-MM-REF36000000;
FDA Recall
Open, Classified
·DAYE (ANNE'S DAY LTD)
Biscuit Factory Business Complex
100 Drummond Road
London United Kingdom·Product code HEB·February 17, 2025
All in One Bundle; Model Number: FG-BNDL-PC-REFAIO;
FDA Recall
Open, Classified
·DAYE (ANNE'S DAY LTD)
Biscuit Factory Business Complex
100 Drummond Road
London United Kingdom·Product code HEB·February 17, 2025
Regular Flow Bundle; Model Number: FG-BNDL-PC-REFRF;
FDA Recall
Open, Classified
·DAYE (ANNE'S DAY LTD)
Biscuit Factory Business Complex
100 Drummond Road
London United Kingdom·Product code HEB·February 17, 2025