TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016.
FDA device recall Z-0659-03 · posted 2003-03-20 · Terminated
Recall details
- Recalling firm
- Interpore Cross International Inc
- Reason for recall
- Instrument fell apart during cleaning prior to surgery.
- Action taken
- Firm telephoned customers on 2/7/2003 requesting that they immediately return thier instruments.
- Root cause
- Other
- Status
- Terminated
- Product code
- LXH
- Quantity affected
- 37 units
- Distribution
- States of NJ, CA, PA, MN, WI, MO, FL, OH, VA, MD, Wash DC, NY, CO, MA and to Brazil, Mexico, England, Denmark, Belgium, Australia.
- Date initiated
- 2003-02-07
- Date posted
- 2003-03-20
- Date terminated
- 2003-08-28
- Location
- Irvine, CA
Monitor recalls programmatically
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