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U.S. Department of Health and Human Services

Medical Device Recalls

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201 to 210 of 500 Results *
Recall Date to: 03/29/2015
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Product Description
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FDA Recall
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LASSO NAV Duo Loop eco Catheters, Catalog No. D-1354-01, D-1354-02, D-1354-03, D-1354-04, D-1354-05,... 2 03/03/2015 Biosense Webster, Inc.
LFT v40 Femoral Head; Catalog Number 6260-9-032; V40 CoCr LFit Head 32mm/-4. Designed to be ass... 2 03/03/2015 Stryker Howmedica Osteonics Corp.
The I-Cart is used to store, transport, and power video equipment used in medical procedures. 2 03/03/2015 Richard Wolf Medical Instruments Corp.
Zip 16 Surgical Skin Closure Device; 16 cm Product number PS1160; Rx only, Sterile Indicated fo... 2 03/02/2015 Zipline Medical
Zip 8M Wound Closure Device; for wounds up to 8 cm in length; Product number PS9080; Rx only, Ste... 2 03/02/2015 Zipline Medical
Zip 8i Surgical Skin Closure Device; for incisions up to 8 cm. Product number PS2080 Indicated ... 2 03/02/2015 Zipline Medical
ADVIA Centaur Systems Progesterone Kit, (5-pack Ref); In Vitro Diagnostic Catalog number: 02177364... 2 03/02/2015 Siemens Healthcare Diagnostics, Inc
ADVIA Centaur Systems Progesterone Kit, (1 -pack) In Vitro Diagnostic; Catalog number: 02382928; SM... 2 03/02/2015 Siemens Healthcare Diagnostics, Inc
ADVIA Centaur Systems Progesterone Kit, (5 -pack); In Vitro Diagnostic; Catalog number: 01586287; SM... 2 03/02/2015 Siemens Healthcare Diagnostics, Inc
ARROW FiberOptix Intra-Aortic Balloon Catheter Kit, 40 cc 7.5 Fr Product Code: IAB-05840-LWS The A... 2 03/02/2015 Arrow International Inc

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