25 results
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48ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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AbClo
FDA UDI
Inventorr MD Inc·07540161750015·
INVENTORR MD INC
FDA registration
INVENTORR MD INC·1 product·🇨🇦 Canada
R2015 RADIUS LOOP
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·November 29, 2018
R2015 RADIUS LOOP
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·November 29, 2018
FISCHER CONE BIOP EX LG
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·December 30, 2022
PROXIMATE*PLUS MD SKIN STPLR
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDT·April 1, 2019
STERILE 4.0 SOFT KOH-EFF
FDA Adverse Event
Malfunction
·COOPERSURGICAL INC.·Product code HEW·October 10, 2018
FISCHER CONE BIOP EX LG
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·December 30, 2022
FISCHER CONE BIOP EX LG
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·December 30, 2022
FISCHER CONE BIOP EX LG
FDA Adverse Event
Malfunction
·COOPERSURGICAL, INC.·Product code HGI·December 30, 2022
Smiths CADD Medication Cassette Reservoir, With clamp and female Luer, Nonvented stopper included, 50 ml PC 4694-24A, REF 21-7001-24, Sterile, Made in Mexico Smith Medical MD, Inc. St Paul, MN 55112 USA
FDA Recall
Terminated
·Smiths Medical MD, Inc.·Product code FPA·June 18, 2007
Smiths CADD Medication Cassette Reservoir, With clamp and female Luer, Nonvented stopper included, 100 ml PC 4695-24A, REF 21-7002-24, Sterile EO, Made in Mexico Smith Medical MD, Inc. St Paul, MN 55112 USA
FDA Recall
Terminated
·Smiths Medical MD, Inc.·Product code FPA·June 18, 2007
Smiths CADD Yellow Medication Cassette Reservoir, With clamp and female Luer, Nonvented stopper included, 100 ml PC 4689-24A, REF 21-7100-24, Sterile, Made in Mexico Smith Medical MD, Inc. St Paul, MN 55112 USA
FDA Recall
Terminated
·Smiths Medical MD, Inc.·Product code FPA·June 18, 2007
Quasar MD Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
FDA Recall
Terminated
·Quasar Bio-Tech, Inc.·Product code OHS·June 29, 2018
TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only
FDA Recall
Open, Classified
·TriMed Inc.·Product code HWC·March 19, 2024
TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only
FDA Recall
Open, Classified
·TriMed Inc.·Product code HWC·March 19, 2024
microTargeting" Drive System, Product Number 66-ZD-MD-01
FDA Recall
Terminated
·FHC, Inc.·Product code HAW·May 10, 2018
microTargeting" Drive System, Product Number 66-ZD-MD
FDA Recall
Terminated
·FHC, Inc.·Product code HAW·May 10, 2018
Deltec Cozmo 3 ml Insulin Cartridge with 0.7mm(22G) x 12.5mm (1/2 in.) needle and cap. Reorder No. 21-1750-24. Immediate container states STERILE EO, Rx Only , Deltec, Inc., St. Paul, MN 55112. Additional labeling states Cartridge is Sterile and nonpyrogenic unless package is opened or damaged. do not use if package is opened or damaged, or if product appears damaged. Made in Mexico for: Deltec 1265 Grey Fox Road, St. Paul, MN 55112 USA, Smiths, smiths Medical - a part of Smiths Group plc.
FDA Recall
Terminated
·Smiths Medical MD, Inc.·Product code LZG·October 15, 2004
Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
FDA Recall
Open, Classified
·O & M HALYARD INC·Product code LZC·April 13, 2026