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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 *
Recall Date to: 04%2F08%2F2014
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POWERSEAL 5 mm, 44 cm, Curved Jaw Sealer and Divider, Double Action is indicated for use in general ... 2 04/30/2024 Olympus Corporation of the Americas
IPS e.max ZirCAD CER/in. Prime A3 C17/5 -A zirconium oxide block for the fabrication of fixed, full... 2 04/30/2024 IVOCLAR VIVADENT AG
IPS e.max ZirCAD CER/in. Prime B1 C17/5 -A zirconium oxide block for the fabrication of fixed, full... 2 04/30/2024 IVOCLAR VIVADENT AG
IPS e.max ZirCAD CER/in. Prime A2 C17/5 -A zirconium oxide block for the fabrication of fixed, full... 2 04/30/2024 IVOCLAR VIVADENT AG
IPS e.max ZirCAD CER/in. Prime C2 C17/5- A zirconium oxide block for the fabrication of fixed, full... 2 04/30/2024 IVOCLAR VIVADENT AG
IPS e.max ZirCAD CER/in. Prime BL1 C17/3- A zirconium oxide block for the fabrication of fixed, ful... 2 04/30/2024 IVOCLAR VIVADENT AG
IPS e.max ZirCAD CER/in. Prime A1 C17/5 - A zirconium oxide block for the fabrication of fixed, ful... 2 04/30/2024 IVOCLAR VIVADENT AG
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 10 Holes, 158 ... 2 04/30/2024 Zimmer, Inc.
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 12 Holes, 184 ... 2 04/30/2024 Zimmer, Inc.
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 16 Holes, 236 ... 2 04/30/2024 Zimmer, Inc.

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