189 results
·
50ms
·
Sources: EU EUDAMED, US FDA
SHERWOOD MEDICAL CO
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code LZH·December 22, 1998
*
FDA Adverse Event
Injury
·*·Product code KYX·February 21, 1997
ARGYLE VASCULAR TOURNIQUET KIT
FDA Adverse Event
SHERWOOD MEDICAL CO.·Product code KCY·July 24, 1996
MONOJECT NEEDLE
FDA Adverse Event
SHERWOOD MEDICAL CO.·Product code FMI·August 20, 1996
SHERWOOD PEG FEEDING TUBE
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code KNT·July 17, 1996
SHERWOOD G-BUTTON
FDA Adverse Event
Other
·SHERWOOD MEDICAL CO.·Product code KNT·July 17, 1996
ARGYLE SALEM SUMP TUBE W/ANIT-REFLUX VALVE
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code KNT·August 16, 1996
ENTRIFLEX TUNGSTEN FEEDING TUBE
FDA Adverse Event
Injury
·SHERWOOD MEDICAL CO.·Product code FPD·July 23, 1996
DOVER ALL SILIOCNE FOLEY CATHETER
FDA Adverse Event
Injury
·SHERWOOD MEDICAL CO.·Product code KOD·September 4, 1996
MONOJECT SYRINGE WITH LUER LOCK-TIP
FDA Adverse Event
SHERWOOD MEDICAL CO·Product code FMF·July 10, 1996
ENTRIFLEX
FDA Adverse Event
Injury
·SHERWOOD MEDICAL CO·Product code KNT·February 28, 2002
ENTRIFLEX
FDA Adverse Event
Injury
·SHERWOOD MEDICAL CO.·Product code KNT·February 28, 2002
NASOGASTRIC FEEDING TUBE
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code FPD·May 24, 1996
MONOJECT SYRINGE
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code FMF·June 13, 1996
EVACUATED COLLECTION NEEDLES
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code JKA·May 22, 1996
MONOJECT STERILE SYRINGE
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code FMF·April 4, 1996
MONOJECT SYRINGE WITH LUER LOCK
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code FMF·June 21, 1996
MONOJECT SYRINGE WITH PLASTIC LUER LOCK TIP
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code FMF·May 7, 1996
MONOJECT SYRINGE
FDA Adverse Event
Malfunction
·SHERWOOD MEDICAL CO.·Product code FMF·April 1, 1996
MONOJECT SAFETY SYRINGE W/SAFETY SHIELD AND NEEDLE
FDA Adverse Event
Injury
·SHERWOOD MEDICAL CO.·Product code FMF·April 26, 1996