Chromphare Surgical Lights
Chromphare Surgical Lights Recall Chromphare surgical lights are being recalled and will be exchanged. This recall affects hospitals, pharmacies, and laboratories in New Zealand that received these devices. The recall is classified as Class I, which is the most serious classification level.
- Recalling firm
- Stryker New Zealand Ltd
- Product
- Chromphare surgical lights. [Device]. Model: Devices manufactured with Soffit Rings. Affected: Part number - CH00000001
- Reason
- The manufacturer has discovered that certain lots of the soffit ring may not adequately support the weight of the ceiling cover. As a result, the cover may shift or slide down the ceiling tube. Movement of the ceiling cover can expose the area above the ceiling, which may allow particles, such as dust, debris, residue, or other contaminants, to enter the sterile field.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-04-13
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/0429f938-3ba5-4f24-b59e-19b15123a5ca