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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-0560-2007 - Alcon Custom-Pak®, part #10975-02, containing BD Beaver® Mini-Blade (part #BD6400 or part #BD6900); individual blades repackaged into custom ophthalmic surgical packs and resterilized by Alcon Laborat...
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2
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03/01/2007
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FEI # 1000117501 Alcon Laboratories, Inc
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Z-0561-2007 - Alcon Custom-Pak®, part #2638-17, containing BD Beaver® Mini-Blade (part #BD6400 or part #BD6900); individual blades repackaged into custom ophthalmic surgical packs and resterilized by Alcon Laborato...
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2
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03/01/2007
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FEI # 1000117501 Alcon Laboratories, Inc
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Z-0564-2007 - Alcon Custom-Pak®, part #11148-02, containing BD Beaver® Mini-Blade (part #BD6400 or part #BD6900); individual blades repackaged into custom ophthalmic surgical packs and resterilized by Alcon Laborat...
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2
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03/01/2007
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FEI # 1000117501 Alcon Laboratories, Inc
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Z-0563-2007 - Alcon Custom-Pak®, part #6515-51, containing BD Beaver® Mini-Blade (part #BD6400 or part #BD6900); individual blades repackaged into custom ophthalmic surgical packs and resterilized by Alcon Laborato...
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2
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03/01/2007
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FEI # 1000117501 Alcon Laboratories, Inc
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Z-0562-2007 - Alcon Custom-Pak®, part #4917-54, containing BD Beaver® Mini-Blade (part #BD6400 or part #BD6900); individual blades repackaged into custom ophthalmic surgical packs and resterilized by Alcon Laborato...
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2
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03/01/2007
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FEI # 1000117501 Alcon Laboratories, Inc
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