SKYLight Imaging Systems, Model 882050; Intended to produce images depicting the anatomical distributions of single phot
FDA device recall Z-0607-2012 · posted 2012-01-11 · Terminated
Recall details
- Recalling firm
- Philips Medical Systems
- Reason for recall
- During preventative maintenance, a crack was discovered in the lower portion of the old style, non-common arm for the detector assembly, which could result in the detector dropping in an uncontrolled manner.
- Action taken
- Urgent Medical Device Correction/Field Safety Notices, dated Dec 08, 2011, were mailed to affected customer sites on December 9th and 12th, 2011 by Return Receipt certified mail. The letter identified the affected product, described the issue and when it could occur, along with the hazards involved. Customers were advised to stop using the system and contact a Philips service representative for an immediate inspection. Customers were also to follow the Instructions For Use to avoid the issue. Philips service will contact customers to arrange a time for Philips to inspect the system. The letter should be placed in the Instructions for Use. The Field Change Order will be released on December 16, 2011. If further information or support is needed, customers should contact Customer Care Solutions Center at 1-800-722-9377.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- KPS
- Quantity affected
- 129
- Distribution
- Worldwide Distribution -- USA, Canada, Italy, Spain, France, United Kingdom, Sweden, Switzerland, Germany, Japan, Denmark, and the Netherlands.
- Date initiated
- 2011-12-08
- Date posted
- 2012-01-11
- Date terminated
- 2012-08-13
- Location
- San Jose, CA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| SKYLIGHT IMAGING SYSTEM (K000908) | Adac Laboratories | 2000-04-05 |