11 results · 12ms · Sources: EU EUDAMED, US FDA

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BD Q-Syte Extension Set, 15 cm, P.V. 0.21 ml, REF 385102, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

Coherent brand DUO Diode Laser Systems. A Non-medical, class IV industrial materials processing machine. The following Model---Serial Numbers (S/N) are affected: P/N 1024403---S/Ns 10026 Through 10088; P.V. -4240/4475---S/Ns 2, 7, 3053, and 10002 through 10024; and P. V. -4458 S/Ns 10019, 10019, 10020, 10043, and 10052.

FDA Recall
Terminated ·Coherent, Inc.·Product code L22·January 19, 2004

BD Q-Syte Extension Set, 15cm Std Bore, P.V. 1.14 ml Luer-Lok, REF 385101, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall
Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

Epix latis GRASPER, 5 mm x 35 cm, REF C4130, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110147

FDA Recall
Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code NWV·March 17, 2020

Epix latis GRASPER, 5mm x 45 cm, REF: C4140, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110154

FDA Recall
Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code NWV·March 17, 2020

Applied Medicals Epix and Direct Drive Laparoscopic Graspers, Model Numbers C4130 and C4140. Used for grasping and manipulating tissue during general or laparoscopic surgery.

FDA Recall
Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa # 3 Rancho Santa·Product code NWV·May 1, 2013

Clarke-Reich Laparoscopic Knot Pusher

FDA Recall
Terminated ·Cook Inc.·Product code NWV·April 25, 2017

Clip Applier Kit, REF: K2887, UDI: (01)30607915139132(17)220822(30)1(10)

FDA Recall
Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code NWV·March 17, 2020

7F NeuroFlo Catheter, Model 1027 The NeuroFlo Catheter is a multi-lumen device with two balloons mounted near the distal tip for the treatment of cerebral ischemia resulting from symptomatic vasospasm following aneurysmal subarachnoid hemorrhage. The NeuroFlo Catheter is under Humanitarian Device Exemption and not commercially released under a premarket notification or premarket approval.

FDA Recall
Terminated ·ZOLL Circulation, Inc.·Product code PAV·April 1, 2014

PS-500 Scope Warmer; 10 units per box. Pre-heating scope for laparoscopy surgery.

FDA Recall
Terminated ·JosNoe Medical, Inc.·Product code NWV·December 1, 2015

DR. THAMES - LAP CHOLE, REF: K0880, UDI: (01)30607915139620

FDA Recall
Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code NWV·March 17, 2020