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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1281-03 - Stanmore modular hip system; Stanmore CoCr femoral size 1 std. stem; part 164241 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1286-03 - Stanmore modular hip system; Stanmore CoCr femoral size 1 straight stem; part 164251 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1282-03 - Stanmore modular hip system; Stanmore CoCr femoral size 2 std. stem; part 164242 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1287-03 - Stanmore modular hip system; Stanmore CoCr femoral size 2 straight stem; part 164252 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1283-03 - Stanmore modular hip system; Stanmore CoCr femoral size 3 std. stem; part 164243 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1288-03 - Stanmore modular hip system; Stanmore CoCr femoral size 3 straight stem; part 164253 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1284-03 - Stanmore modular hip system; Stanmore CoCr femoral size 4 std. stem; part 164244 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1289-03 - Stanmore modular hip system; Stanmore CoCr femoral size 4 straight stem; part 164254 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1285-03 - Stanmore modular hip system; Stanmore CoCr femoral size 5 std. stem; part 164245 2 09/24/2003 FEI # 1825034
Biomet, Inc.
Z-1290-03 - Stanmore modular hip system; Stanmore CoCr femoral size 5 straight stem; part 164255 2 09/24/2003 FEI # 1825034
Biomet, Inc.
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