Medical Device Recalls
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1 to 10 of 14 Results
Related Medical Device Recalls |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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