Kodak DirectView DR 7100 System, Catalog #133-6049, a digital radiology system. The major system components are: operato
FDA device recall Z-0728-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Eastman Kodak Co
- Reason for recall
- Defective component in overhead tube support balancer may cause the suspended load to fall.
- Action taken
- 2/20/2004: Field representatives notified the customer in China that the unit should not be used until the OTS Balancer component can be repaired/replaced.
- Root cause
- Other
- Status
- Terminated
- Product code
- KPR
- Quantity affected
- 3 units
- Distribution
- Amsterdam, China and Kuwait.
- Date initiated
- 2004-02-20
- Date posted
- 2004-07-20
- Date terminated
- 2004-05-28
- Location
- Rochester, NY
Monitor recalls programmatically
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| DR5000 DEDICATED CHEST X-RAY SYSTEM (K001341) | Analogic Corp. | 2000-06-02 |