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Sources: EU EUDAMED, US FDA
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Stryker CBCII Blood Conservation Kit w/ 1/8 in. (3.2mm) Round PVC Drain and Curved Trocar, sterile, Stryker Instruments, Kalamzoo, MI; REF 225-28-514. Blood recovery system used post-operatively to collect, filter and allow for reinfusion of autologous blood.
FDA Recall
Terminated
·Stryker Instruments Div. of Stryker Corporation·Product code cac·November 12, 2009
Stryker CBC ConstaVac Blood Conservation Kit 3/16in. (4.8mm) PVC, sterile, Stryker Instruments, Kalamazoo, MI REF 225-426-W. Blood recovery system used post-operatively to collect, filter and allow for reinfusion of autologous blood.
FDA Recall
Terminated
·Stryker Instruments Div. of Stryker Corporation·Product code cac·November 12, 2009
Stryker CBCII with Quick Disconnect and 3/16 in. Double Trocar, sterile, Stryker Instruments, Kalamazoo, MI, REF 225-28-S5. Blood recovery system used post-operatively to collect, filter and allow for reinfusion of autologous blood.
FDA Recall
Terminated
·Stryker Instruments Div. of Stryker Corporation·Product code cac·November 12, 2009
Zimmer H.A.S. Autotransfusion System, H.A.S. Kit with 3/16" Soft Drain , 4,8mm, 15Fr, PVC, 107cm, firm, sterile, latex free, Rx only; Zimmer, Swindon, Wiltshire, United Kingdom; Zimmer, Dover, Ohio; REF 00-2555-030-05.
FDA Recall
Terminated
·Zimmer Inc.·Product code CAC·January 29, 2008
The box label states: "AT1 Autotransfusion Set 9005101 STERILE...FRESENIUS KABI...Fresenius Kabi AG 61345 Bad Hamburg Germany...Federal (USA) Law restricts this device to sale by or on order of a physician". The AT1 Autotransfusion Set is distributed by Fresenius Kabi on its own or as part of a ATF40 kit or ATF120 kit. AT1 Autotransfusion set is a disposable set, dedicated component of the Fresenius CATS Continuous Autotransfusion System, which in turn is an Autotransfusion device for the processing of autologous shed blood collected intraoperatively and postoperatively to obtain washed packed red blood cells for reinfusion.
FDA Recall
Terminated
·Fresenius Kabi, LLC·Product code CAC·March 29, 2010
Haemonetics Cell Saver 5 Low Volume (125mL) Fast Pack List Number: 265
FDA Recall
Terminated
·Haemonetics Corporation·Product code CAC·December 17, 2002
Haemonetics Basic Low Volume (125ml) Cell Saver 5 Bowl Set List Number: 261
FDA Recall
Terminated
·Haemonetics Corporation·Product code CAC·December 17, 2002
Autovac TL. Autotransfusion System for Orthopedic Wound Drainage. The product is shipped in cartons containing 6 units
FDA Recall
Terminated
·Boehringer Laboratories Inc·Product code CAC·November 7, 2003
ASY, Brat Pack Procedure Set
FDA Recall
Terminated
·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005
ASY Brat 2 Procedure Set
FDA Recall
Terminated
·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005
High Speed Cell Saver5/5+ Bowl Set Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
FDA Recall
Terminated
·Haemonetics Corporation·Product code CAC·October 21, 2019
CS5/5+ Fastpacks, 225 mL, 20 Res Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.
FDA Recall
Terminated
·Haemonetics Corporation·Product code CAC·October 21, 2019
Express Dry Seal Chest Drains (Express): 4000-100N DRAIN, EXPRESS, SINGLE; 4050-100N DRAIN, EXPRESS, BRU
FDA Recall
Open, Classified
·Atrium Medical Corporation·Product code CAC·September 18, 2023
Oasis Dry Suction Water Seal Chest Drains (Oasis): (1)3600-100 DRAIN, OASIS SINGLE W/AC; (2)3612-100 DRAIN, OASIS PEDI A/C; (3)3650-100 DRAIN, OASIS BRU W/AC;
FDA Recall
Open, Classified
·Atrium Medical Corporation·Product code CAC·September 18, 2023
Haemonetics OrthoPAT System-OPAT QuickConnect Reservoirs. Product Code: OPT-R-1000 The OrthoPAT orthopedic perioperative autotransfusion system indicated for use to salvage RBCs from blood lost intraoperatively and postoperatively during surgical procedures
FDA Recall
Terminated
·Haemonetics Corporation·Product code CAC·July 13, 2018