9 results · 56ms · Sources: EU EUDAMED, US FDA

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HEPARIN LOCK FLUSH 10 USP UNITS/ML

FDA Adverse Event
Injury ·APP PHARMACEUTICALS LLC·Product code NZW·March 16, 2012

DIPRIVAN

FDA Adverse Event
Injury ·APP PHARMACEUTICALS, LLC·Product code FMF·October 6, 2008

DEXAMETHASONE SODIUM PHOSPHATE INJECTION, USP

FDA Adverse Event
Malfunction ·APP PHARMACEUTICALS, LLC·Product code KYX·April 18, 2011

HEPARIN LOCK FLUSH SOLUTION, USP, 10 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-544-01, Product Code 504401, Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.

FDA Recall
Terminated ·App Pharmaceuticals Llc·Product code NZW·May 20, 2010

HEPARIN LOCK FLUSH SOLUTION, USP, 100 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-545-01, Product Code 504501; and HEPARIN LOCK FLUSH SOLUTION, USP, 100 USP Units/mL, 5 mL Multiple Dose Vial, 500 USP Units/5 mL, plastic vial, vial size 6 mL, NDC 63323-545-05, Product Code 504505; Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.

FDA Recall
Terminated ·App Pharmaceuticals Llc·Product code NZW·May 20, 2010

HEPARIN LOCK FLUSH SOLUTION, USP, 100 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-545-01, Product Code 504501; and HEPARIN LOCK FLUSH SOLUTION, USP, 100 USP Units/mL, 5 mL Multiple Dose Vial, 500 USP Units/5 mL, plastic vial, vial size 6 mL, NDC 63323-545-05, Product Code 504505; Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.

FDA Enforcement
Class II ·Terminated·App Pharmaceuticals Llc·June 27, 2012

HEPARIN LOCK FLUSH SOLUTION, USP, 10 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-544-01, Product Code 504401, Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.

FDA Enforcement
Class II ·Terminated·App Pharmaceuticals Llc·June 27, 2012

SUNGO Europe B.V.

Authorized representative
🇳🇱 Netherlands·1571 Manufacturers·20390 Devices

MedNet EC-REP GmbH

Authorized representative
🇩🇪 Germany·464 Manufacturers·5263 Devices