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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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Z-0532-2009 - Depuy DELTA Xtend, Standard humeral PE Cup Dia 38/+3 STD, sterile, Depuy France; REF 130738203.
The device is used as a shoulder implant.
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2
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01/15/2009
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Depuy Orthopaedics, Inc.
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Z-0533-2009 - Depuy DELTA Xtend, Standard Humerus PE Cup, Dia 38/+6 STD, sterile, Depuy France; REF 130738206.
The device is used as a shoulder implant.
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2
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01/15/2009
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Depuy Orthopaedics, Inc.
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Z-0534-2009 - Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 38/+9 STD, sterile, Depuy France; REF 130738209.
The device is used as a shoulder implant.
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2
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01/15/2009
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Depuy Orthopaedics, Inc.
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Z-0539-2009 - Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42+6R RET, sterile, Depuy France; REF 130742106.
The device is used as a shoulder implant.
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2
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01/15/2009
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Depuy Orthopaedics, Inc.
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Z-0536-2009 - Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+3 STD, sterile, Depuy France; REF 130742203.
The device is used as a shoulder implant.
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2
|
01/15/2009
|
Depuy Orthopaedics, Inc.
|
Z-0537-2009 - Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+6 STD, sterile, Depuy France; REF 130742206.
The device is used as a shoulder implant.
|
2
|
01/15/2009
|
Depuy Orthopaedics, Inc.
|
Z-0538-2009 - Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+9 STD, sterile, Depuy France; REF 130742209.
The device is used as a shoulder implant.
|
2
|
01/15/2009
|
Depuy Orthopaedics, Inc.
|
Z-0535-2009 - Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 38/+6R RET, sterile, Depuy France; REF 130738106.
The device is used as a shoulder implant.
|
2
|
01/15/2009
|
Depuy Orthopaedics, Inc.
|