Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16227 |
| Brand Name: | Kodak 2100 and 2200 Intraoral X-ray System |
| Model: | Kodak 2100 & 2200 Intraoral X-Ray System |
| Affected: | Manufactured in China between May 2008 and April 2010 |
| Software version: | |
| Recalling Organisation: | Carestream Health New Zealand Ltd c/- Quigg Partners Level 7, 28 Brandon St Wellington |
| Contact Information: | 021 977 215 |
| Manufacturer: | Carestream Health Inc (HCIS) |
| Issue: | The manufacturer advises that it has received advice that there were five incidents overseas where an early failure of the device occurred where pivot/bracket of the arm broke allowing the arm to drop to 90°. The failure is not immediate and would be noted by the user as part of the routine maintenance inspection, before the arm can fall. Should the arm fall, there is a risk of injury by impact to the patient or user. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 14/2/2014 |
