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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
Related Medical Device Recalls Recall Date to: 07%2F04%2F2014
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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... 2 03/01/2007 Alcon Laboratories, Inc
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... 2 03/01/2007 Alcon Laboratories, Inc
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... 2 03/01/2007 Alcon Laboratories, Inc
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... 2 03/01/2007 Alcon Laboratories, Inc
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... 2 03/01/2007 Alcon Laboratories, Inc
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