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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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MERIDIAN (model nos. 476, 976, 1176 and 1276) pacemaker. Sterilized with gaseous ethylene oxide. ...
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1
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07/28/2005
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Guidant Corporation
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MEDLINE convenience kits labeled as:
1) MAJOR VASCULAR-LF, REF CDS840232L;
2) AVF-LF, REF CDS8402...
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2
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12/05/2024
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MEDLINE INDUSTRIES, LP - Northfield
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MEDLINE Kits, trays, and packs labeled as follows:
a) DIALYSIS FISTULA KIT, REF DYNDC3106,
b) E...
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1
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02/25/2024
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MEDLINE INDUSTRIES, LP - Northfield
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Locking Tear-Away Sheath Introducer Product Line.
ACCUGUIDE SINGLE LUMEN 4FR PICC P460K 5/;
P56...
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2
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08/03/2005
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B. Braun Medical, Inc.
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Kappa Model 901 Implantable Pulse Generators (IPGs) are pacemaker devices that provide therapies for...
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2
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07/20/2004
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Medtronic Inc. Cardiac Rhythm Managment
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Kappa Model 701 Implantable Pulse Generators (IPGs) are pacemaker devices that provide therapies for...
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2
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07/20/2004
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Medtronic Inc. Cardiac Rhythm Managment
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Insignia Plus Multiprogrammable Pacemaker, DDDR Model 1295
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2
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05/29/2003
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Guidant Corp-Cpi Division
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Insignia Plus Multiprogrammable Pacemaker, DDDR Model 1294
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2
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05/29/2003
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Guidant Corp-Cpi Division
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Insignia Plus Multiprogrammable Pacemaker, DDD Model 986
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2
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05/29/2003
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Guidant Corp-Cpi Division
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Insignia Plus Multiprogrammable Pacemaker, DDD Model 985
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2
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05/29/2003
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Guidant Corp-Cpi Division
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