295 results · 27ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

All Med Medical 22ga x 1.5" Winged Administration Set w/Y Site Model # M2215Y Reorder # 50-2242

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·August 30, 2010

Civco, MTSR02 Shoulder Retractor with Sherpa Wrist Loops Kit with Base, Non-sterile re-usable wool wrist strap, REF: 20SR02SUB2, Rx Only, The devise is intended to pull patients shoulders down for clearance when treating lateral fields to the neck.

FDA Recall
Terminated ·Med Tec Inc·Product code FMQ·December 11, 2014

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR AND 7 FT. OXYGEN TUBING, REF CPRM1126

FDA Recall
Terminated ·Sun Med, LLC·Product code BTM·May 24, 2018

Vista Dental Products Chlor-XTRA - 12mL Prefilled Syringes, QTY: 8, REF 503850

FDA Recall
Terminated ·Inter-Med Llc·Product code KJJ·June 27, 2019

Sit to Stand STS500 Patient Lift

FDA Recall
Open, Classified ·Med-Mizer, Inc.·Product code FSA·February 3, 2023

Sideport Kit w/Oxygen Line, consisting of an adjustable sideport valve, an O2 port elbow and O2 supply tubing; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83167

FDA Recall
Terminated ·VIASYS Med Systems·Product code CAI·September 10, 2003

Sideport Kit, consisting of an adjustable sideport valve and an O2 port elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83166

FDA Recall
Terminated ·VIASYS Med Systems·Product code CAI·September 10, 2003

All Med Medical 20ga x .75" Winged Administration Set w/Y Site Model # M2075Y Reorder # 50-2022

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·August 30, 2010

All Med Medical 19ga x 1.50" RA Hub Needle Model #M1915H Reorder #55-1940 Intended to be used to inject fluids into, withdraw fluids from inside the vascular space through a subcutaneously implanted port.

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·August 30, 2010

All Med Medical 22ga x .75" Winged Administration Set w/Y Site Model # M2275Y Reorder # 50-2222

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·August 30, 2010

All Med Medical 20ga x 1.5" RA Hub Needle Model #M2015H Reorder #55-2040 Intended to be used to inject fluids into, withdraw fluids from inside the vascular space through a subcutaneously implanted port.

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·August 30, 2010

All Med Medical 22ga x .75" Standard Bore Winged Administration Set Model # M2275S Reorder # 50-2223

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·August 30, 2010

Marquette Medical Huber Trap-A Safety Huber Needle 20ga x .75" Winged Administration Set w/Y Site Model # MW203Y Intended to be used to inject fluids into, withdraw fluids from inside the vascular space through a subcutaneously implanted port.

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·August 30, 2010

Marquette Medical Huber Trap-A Safety Huber Needle 22ga x 1 Winged Administration Set w/Y Site Model # MW221Y Intended to be used to inject fluids into, withdraw fluids from inside the vascular space through a subcutaneously implanted port.

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·August 30, 2010

22ga x 1" Right Angle Huber Needle This product is a small gauge needle intended for single use hypodermic access to implanted ports.

FDA Recall
Terminated ·Multi-Med, Inc.·Product code FMI·May 26, 2010

Product is a surgical device packaged in a box which is labeled as Sterile with the following identification: ''PMII PROLENE Mesh Polypropylene Nonabsorbable Synthetic surgical Mesh ETHICON'' Additional infomation including comparisons between authentic Ethicon product and counterfeit are available at the following website: www.ethicon.com

FDA Recall
Terminated ·Q-Med Corporation·Product code FTL·October 30, 2003

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, TUBE RESERVOIR, CO2 AND 7 FT. OXYGEN TUBING, REF CPRM1126C

FDA Recall
Terminated ·Sun Med, LLC·Product code BTM·May 24, 2018

STAT-Check MANUAL RESUSCITATOR / VENTILATOR, REF SC9200MBP-1

FDA Recall
Terminated ·Sun Med, LLC·Product code BTM·May 24, 2018

Stackhouse FreedomAire Lens/Hood; a sterile disposable protective head garment for use with the FreedomAire Surgical Helmet System, providing a clear plastic bubble lens and protective head hood to connect to the surgical helmet; individually packaged hoods, 12 per case; Manufactured for Viasys MedSystems, Wheeling, IL 60090

FDA Recall
Terminated ·VIASYS Med Systems·Product code FXY·September 13, 2005

Hyperinflation Circuit, consisting of a 2.0 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve and ported elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83120

FDA Recall
Terminated ·VIASYS Med Systems·Product code CAI·September 10, 2003