Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K031693 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Mallory Head Calcar Femoral 55 mm resection/porous coated 15.0 mm x 220 mm left stem, Sterile, REF 1... | 2 | 05/26/2010 | Biomet, Inc. |
17 mm Mallory Head Calcar 45 mm repl. fmrl. /100% porous 18.5 mm minimum ream dia x 260 mm rt., Ster... | 2 | 05/26/2010 | Biomet, Inc. |
17 mm Mallory Head Calcar 55 mm repl. femoral/100% porous 18.5 mm minimum ream dia. x 220 mm rt., S... | 2 | 05/26/2010 | Biomet, Inc. |
19 mm Mallory Head Calcar 45 mm repl. femoral/100% porous 20.5 mm minimum ream dia. x 260 mm rt., S... | 2 | 05/26/2010 | Biomet, Inc. |
19 mm Mallory Head Calcar 55 mm repl. femoral/100% porous 20.5 mm minimum ream dia. x 260 mm lt.., ... | 2 | 05/26/2010 | Biomet, Inc. |
M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedures... | 2 | 12/17/2020 | Biomet, Inc. |
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