FDA Recall
Terminated
Portex Hypodermic Needle-Pro Syringe and Needle 1ml/LS Small Gauge Safety 27 g x 1/2'' Reference Number: 4313
Recall: Z-1078-04
·
Initiated June 29, 2004
Recall
- Recall Number
- Z-1078-04
- Event Number
- 29498
- Firm
- Smiths Medical ASD, Inc.
- FEI Number
- 1217052
- Product Code
- FMI
- Status
- Terminated
- Root Cause
- Other
- Initiated
- June 29, 2004
- Posted
- July 20, 2004
- Terminated
- May 2, 2006
- Address
- 10 Bowman Dr, Keene, NH, 03431-5043
Description
Portex Hypodermic Needle-Pro Syringe and Needle 1ml/LS Small Gauge Safety 27 g x 1/2'' Reference Number: 4313
Reason
Sterility of product is not assured
Action
Smiths Medical notified consignees by telephone on June 29, 2004. The consignees were asked to immediately quarantine their stock . The Dealers and direct customers were contacted via letter delivered by Federal Express on July 2, 2004.
Distribution
Nationwide
Quantity
180 CASES (400/CS)