35 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Terminated
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Terumo Perfusion System 8000 Base, 5 pump, 115v; Model 8000; Catalog No. 16401.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Terumo Perfusion System 9000, 100v, with color screen; Model 9000; Catalog No. 164280.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Terumo Perfusion System 8000 Base, 5 pump, 220240v; Model 8000; Catalog No. 16406.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 8000; Catalog No. 16400.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·January 12, 2007
Terumo Perfusion System 8000 Base, 5 pump, 100v, Model 8000; Catalog No. 16410.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·January 12, 2007
Terumo Perfusion System 8000 Base, 4 pump, 220/240v; Model 8000; Catalog No. 16405.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Terumo Perfusion System 8000 Base, 4 pump, 100v, Model 8000; Catalog No. 16409.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Terumo Perfusion System 9000, 115v, with color screen; Model 9000; Catalog No. 164300.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Terumo Perfusion System 8000 Base, 5 pump, 115v; Model 8000; Catalog No. 16401.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·January 12, 2007
Terumo Perfusion System 8000 Base, 5 pump, 220/240v; Model 8000; Catalog No. 16406.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·January 12, 2007
Terumo Perfusion System 8000 Base, 4 pump, 220/240v; Model 8000; Catalog No. 16405.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·January 12, 2007
Terumo Perfusion System 8000 Base, 5 pump, 100v, Model 8000; Catalog No. 16410.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Manual Drive Unit for Sarns (Terumo) Centrifugal Perfusion System; Catalog No. 164268.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 8000; Catalog No. 16400.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
Terumo Perfusion System 9000, 220/240v, with color screen; Model 9000; Catalog No. 164290.
FDA Recall
Terminated
·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006
MAGELLAN 25x5/8 TW CLEAR HUB BULK, Non Sterile Product Number: 7777851558
FDA Recall
Terminated
·Kendall Healthcare Products Co·Product code FMI·October 8, 2004
CONTI ECHO CT W/2IN TUOHY ULTRA 360 SET, Material Number 331767 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.
FDA Enforcement
Class II
·Terminated·B. Braun Medical, Inc.·October 10, 2018
BD Nokor Admix Needle 16 G x 1 TW (1.6mm x 25mm) REF 305216 Sterile BD, Franklin Lakes, NJ MADE IN USA For use in aspiration of medications, typically in the pharmacy setting.
FDA Recall
Terminated
·Becton Dickinson & Company·Product code FMI·March 1, 2011
Acetabular Pressurizer; single use and six units per box. The Acetabular Pressurizer 0206-522-000 is an accessory to the Advanced Cement Mixer (ACM). The Acetabular Pressurizer Tiplet P/N 0206-522-012 is sealed in a two pouches, sterilized, and labeled as part number 0206-522-000. This Acetabular Pressurizer is an accessory used to pressurize the cement applied to the prosthesis to be implanted during the surgery. The Acetabular Pressurizer is an injection molded component made with resin material DOW HDPD 10462N which is a rigid plastic once it is molded.
FDA Enforcement
Class II
·Terminated·Stryker Instruments Div. of Stryker Corporation·November 20, 2013
ITW Dymon Medaphene Plus Disinfectant Spray, Pseudomonacidal, Virucidal, Mildewcidal, Fungicidal, Staphylocidal, Tuberculocidal, packaged in 20-oz. steel aerosol cans, net wt 16-oz. (1-lb.), 12 cans/case, containing 0.19% o-phenylphenol and 68.00% ethyl alcohol, Product 34720. The firm name on the label is ITW Dymon, Olathe, KS. The product is also sold under the following private labels: (1) Renown Disinfectant Deodorant II, Product REN05013, Distributed by AmSan, LLC, Deerfield, IL; (2) Decon Aerosol Disinfectant, Catalog #8617, Manufactured For Decon Labs, Inc., Bryn Mawr, PA; (3) New Jax Medaphene Plus Disinfectant Spray, Sold By Newell Paper Company, Hattiesburg, MS, Columbus, MS, Meridian, MS; (4) San-O-Phene Plus Disinfectant Spray, Sold By San Joaquin Supply Co., Fresno, CA; (5) Sterling Quality Hospital Use Micro II Disinfectant Spray, Distributed By Sterling Sanitary Supply Corporation, Woodside, NY; (6) Ball-Phene Spray Disinfectant, Reorder #3U037, Manufactured for W.W. Grainger, Inc., Lake Forest, IL; (7) Area Two-In-One Disinfectant Spray Original, Sold By Area Distributors, Inc., Quincy, IL; (8) Benefax Disinfectant Spray, Exclusively Sold By Biotek Corporation, Melrose Park, IL; (9) Pheno-Cen Spray Disinfectant/Deodorant, Sold By Central Solutions, Inc., Kansas City, KS; (10) Clark Bio-Phene Plus Disinfectant/Spray, Sold By Clark Paper Plus Inc., Carteret, NJ; (11) LOGIChem Hosp-I-Septic Disinfectant Spray, Distributed Exclusively For Edmar, Woodside, NY; (12) Morcept Hospital Disinfectant, Sold By Moore Research, Inc., St. Louis, MO; (13) Pro Chem Deocept Purity Hospital Disinfectant, Sold By Pro-Chem, Inc., Alpharetta, GA; (14) Select Specialty Products Spectrum II Hospital Type Disinfectant, Sold By Select Specialty Products, Charlottesville, VA.
FDA Recall
Terminated
·ITW Dymon·Product code LRJ·February 15, 2005