8 results
·
55ms
·
Sources: EU EUDAMED, US FDA
FREESTYLE 28-GUAGE STERILE LANCETS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC.·Product code FMK·August 21, 2020
TANDEM MOBI
FDA Adverse Event
Injury
·TANDEM DIABETES CARE INC.·Product code QFG·May 29, 2025
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·June 23, 2025
MCRYL UD 18IN 3-0 S/A PS-2 PRM MP
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAN·July 22, 2024
MCRYL UD 18IN 3-0 S/A PS-2 PRM MP
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAN·July 22, 2024
Hospira Blood Set, with 200 Micron Filter, 80 Inch, Non-DEHP; an Rx sterile medical device used to administer blood products; 48 individually wrapped sets per case; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 USA; list 14203-28. Intended use: for the administration of blood products.
FDA Recall
Terminated
·Hospira Inc.·Product code FPA·January 12, 2012
LifeShield Primary Plumset, CLAVE port, CLAVE Y-Site, 104 inch, 15 drops/mL, 48 sets per case; a sterile Rx device; Hospira Inc, Lake Forest, IL USA. Made in Costa Rica; product 120300412, list number 12030-12. Product Usage: For administration of I.V. fluids.
FDA Recall
Terminated
·Hospira Inc.·Product code FRN·April 25, 2012
mdi Europa GmbH
Authorized representative
🇩🇪 Germany·132 Manufacturers·4741 Devices