0003 - 4060-2 KIT
Report
- Report Number
- 2023141-2009-00002
- Event Type
- Malfunction
- Date Received
- January 21, 2009
- Date of Event
- October 10, 2008
- Report Date
- January 21, 2008
- Manufacturer
- ZIMMER DENTAL INC.
- Product Code
- LYC
- PMA / PMN Number
- K811101
- Removal / Correction Number
- 2023141-01/19/2009-001R
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
FINDINGS: COMPLAINT CANNOT BE VERIFIED. VISUAL INSPECTION FOUND THAT VIALS WERE RETURNED IN A PLASTIC BAG EMPTY. NO CHIPS WERE FOUND ON RETURNED VIALS. GLASS CHIP WAS RETURNED IN A SEPARATE PLASTIC BAG. LOT TRACING WAS COMPLETED AND WAS FOUND ACCEPTABLE TO RELEASE CRITERIA. THE THREE LOTS LISTED IN THE ADDITIONAL INFORMATION SECTION OF THE 3500A WILL BE THE SUBJECT OF A REMOVAL, REPORTED TO A (B) (4) DISTRICT OFFICE BY THE ZIMMER CORPORATE STAFF. 2023141-01/19/2009-001R. THIS 3500A FORM IS BEING FILED MORE THAN 30 DAYS AFTER THE RECEIPT OF THE COMPLAINT INFORMATION. NO INJURY WAS INVOLVED IN THE COMPLAINT REPORTED. UPON COMPLETION OF OUR INVESTIGATION, IT WAS DETERMINED THAT A REMOVAL ACTION WOULD BE UNDERTAKEN AND REPORTED TO THE FDA. THIS MDR IS BEING FILED IN CONJUNCTION WITH THAT REPORTABLE REMOVAL ACTION. ADDITIONAL LOT NUMBERS & MANUFACTURED DATES: 60967942 - 04/04/2008 AND 60864773 - 11/30/2007.
DISTRIBUTOR REPORTED THAT A FRAGMENT OF THE GLASS VIAL WAS MIXED IN THE CALCITIE. NO PATIENT INVOLVEMENT OR IMPACT WAS REPORTED. THE DISTRIBUTOR DID NOT PROVIDE FURTHER INFORMATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 0003 - 4060-2 KIT | PARTICLES, CALCITITE | LYC | ZIMMER DENTAL INC. | NA | 60879983 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |