A1272-17 Portex Epidural Mini-pack
FDA device recall Z-0250-06 · posted 2005-11-30 · Terminated
Recall details
- Recalling firm
- Smiths Medical ASD, Inc.
- Reason for recall
- Tray may contain holes compromising the sterility of the device
- Action taken
- Smiths Medical ASD notffied accounts by letter via UPS or Fedex on November 17, 2005. Customers and dealers are directed to fax back the attached Reply Letter to Smiths Medical, Keene even if the customer/dealer no longer has affected products in inventory
- Root cause
- Other
- Status
- Terminated
- Product code
- CAZ
- Distribution
- Nationwide
- Date initiated
- 2005-11-17
- Date posted
- 2005-11-30
- Date terminated
- 2012-05-08
- Location
- Keene, NH
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