Portex Hypodermic Needle-Pro Syringe & Needle 3mL/LL 25G x1'' Catalog Number: 4238
FDA device recall Z-0858-05 · posted 2005-06-01 · Terminated
Recall details
- Recalling firm
- Smiths Medical ASD, Inc.
- Reason for recall
- Mislabeled: Product may contain an incorrect needle size. Product labeled as a 25G x 1" may contain a 25G x 5/8"
- Action taken
- Smith Medical notified dealers of the recall on May 5, 2005 by telephone. The remaining customers were notified on May 12, 2005 by telephone. Follow-up letter delivered by Federal Express on May 17, 2005.
- Root cause
- Other
- Status
- Terminated
- Product code
- FMI
- Quantity affected
- 159 cases (400 per case) =63,600 each.
- Distribution
- Nationwide
- Date initiated
- 2005-05-05
- Date posted
- 2005-06-01
- Date terminated
- 2012-05-08
- Location
- Keene, NH
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