Products are various dental surgical drills packed in a sealed tray and labeled as sterile. The tray is labled as follow
FDA device recall Z-0385-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Implant Innovations, Inc.
- Reason for recall
- The tray lid seals may be open thereby compromising the sterility barriers for the recalled lots.
- Action taken
- The firm notified international distributors on 12/2/2003 via e-mail and also a recall notification letter was faxed to them on 12/2/2003. They were instructed to subrecall to the health professional level. Also on 12/2/2003 all domestic accounts (health practioners) were telephoned and then faxed a recall notification letter. Each account was instructed to check their inventory, respond back by fax and to return recalled product to Implant Innovations Inc.
- Root cause
- Other
- Status
- Terminated
- Product code
- DZI
- Quantity affected
- 16
- Distribution
- Product was distributed to 45 Dentist/Surgeons nationwide in the US and also to 13 international Distributors in Canada, Sweden, Germany, Colombia, Spain, Switzerland, Australia, Japan, Austria, Franc
- Date initiated
- 2003-12-02
- Date posted
- 2004-07-20
- Date terminated
- 2009-10-05
- Location
- Palm Beach Gardens, FL
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