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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 14 Results
Related Medical Device Recalls
 
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Product Description
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Recall
Class
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FDA Recall
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Z-0242-06 - 4902 Glass L.O.R. Syringe 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0243-06 - 4903 Glass L.O.R. Syringe 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0244-06 - 4904 Glass L.O.R. Syringe 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0245-06 - 4950-16 Portex® Epidural Mini-pack 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0246-06 - 4950-17 Portex® Epidural Mini-pack 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0247-06 - 4950-18 Portex® Epidural Mini-pack 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0255-06 - A3176-18 Portex® Epidural Mini-pack 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0249-06 - 4954-17 Portex® Epidural Mini-pack 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0250-06 - A1272-17 Portex® Epidural Mini-pack 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
Z-0251-06 - A1378-18 Portex® Epidural Mini-pack 2 11/30/2005 FEI # 1217052
Smiths Medical ASD, Inc.
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