FDA Recall
Terminated
Dr. Fog Endoscopic fog prevention kit.
Recall: Z-0897-05
·
Initiated May 15, 2005
Recall
- Recall Number
- Z-0897-05
- Event Number
- 32092
- Firm
- Aspen Surgical Products, Inc.
- FEI Number
- 3002750084
- Product Code
- KOG
- Status
- Terminated
- Root Cause
- Process control
- Initiated
- May 15, 2005
- Posted
- June 16, 2005
- Terminated
- September 16, 2005
- Address
- 7425 Clyde Park Ave Sw, Ste G, Byron Center, MI, 49315-8373
Description
Dr. Fog Endoscopic fog prevention kit.
Reason
An improper expiration date was placed on the individual packages, although the dispenser box and carton contained the correct expiration date.
Action
Consignees were notified via phone on 5/15/05. Wholesalers were requested to notify their customers.
Distribution
Nationwide.
Quantity
2460 packages.