Atkinson Retrobulbar Anesthesia Needles, 25 gauge 1 1/2". Catalog Number 8065420920. The product is sold in boxes that c
FDA device recall Z-1197-2007 · posted 2007-08-25 · Terminated
Recall details
- Recalling firm
- Alcon Research, Ltd
- Reason for recall
- Mislabeled: boxes actually contained Tri-Fact needles
- Action taken
- The recalling firm telephoned the hospital on 7/11/07 to inform them of the problem and the need to return the product. As a follow up to the telephone call, the recalling firm issued a recall letter via FedEx on 7/11/07. The firm's representative is making arrangements to pick up the recalled product.
- Root cause
- Process control
- Status
- Terminated
- Product code
- HMX
- Quantity affected
- 2 boxes
- Distribution
- CA.
- Date initiated
- 2007-07-11
- Date posted
- 2007-08-25
- Date terminated
- 2007-08-28
- Location
- Fort Worth, TX
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