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U.S. Department of Health and Human Services

Medical Device Recalls
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131 to 140 of 500 Results *
Product: ece Recall Date to: 06/05/2014
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NOCTURNAL ELITE CARE CLINER 6980(STD)/6990(X-LG) products are labeled in part: "***NOCTURNAL ELITE ... 2 04/25/2012 Winco Mfg., LLC
PFC Steinman Pin/Drill Pack Sterile (WPC 667-2012) Drill Bit and Steinman Pin Packet (1 unit) The... 2 04/16/2012 DePuy Orthopaedics, Inc.
Integra Endoscopic Gastrocnemius Release (EGR) System. The device consists of one (1) unit which is ... 2 03/19/2012 Integra LifeSciences Corp.
Pelton & Crane Spirit 3000 dental operative unit with the TLC SAFEdrive option, 1727 Fuehauf Dr. Cha... 2 03/06/2012 Pelton & Crane Company
REF 42-422561 SIGNATURE QTY, 1 TKA GDE/MDL (Prosthesis, knee) SET 04-05 DGHUMPHR-NOV52LKA-J_K-004320... 2 03/02/2012 Biomet, Inc.
Therakos Cellex Photopheresis System CellexUSA & Cellex. The photopheresis system is indicated f... 2 01/11/2012 Therakos, Inc.
Lifescreen Apnea is Lifescreen ECG Screening System, Version 3.31. Lifescreen Apnea is indicate... 2 01/11/2012 Del Mar Reynolds Medical, Ltd.
Product is 40mm Flexible Tube. ***NON-STERILE PRODUCT***CAUTION: FEDERAL LAW RESTRICTS THIS DEVICE ... 2 01/11/2012 Walter Lorenz Surgical, Inc.
SoftPath GUI Versions: 4.3.0.10, 4.3.0.11, and 4.3.0.12. SoftPath is a laboratory information sy... 2 12/02/2011 SCC Soft Computer
SoftPath GUI versions: 4.2.3.3-4.2.3.6 and 4.3.0.5-4.3.0.12. SoftPath is a laboratory information... 2 12/02/2011 SCC Soft Computer

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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