Case V7.0 Cardiac Testing Systems
Recall Summary GE Medical Systems Information Technologies Inc is recalling CASE v7.0 Cardiac Testing Systems distributed to hospitals, pharmacies, and laboratories in New Zealand. The manufacturer will issue guidance on how to use the device. This is classified as a Class I recall, indicating a serious issue.
- Recalling firm
- GE Healthcare Limited
- Product
- CASE v7.0 Cardiac Testing Systems. [Device]. Model: CASETM v7– Thermal Printer Assembly - product code - SU3
- Reason
- The manufacturer has become aware of a potential for electrical sparking at the printer head of CASE v7 Systems. In the unlikely situation that the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charring or discoloration of the thermal printer paper. In rare cases, ignition of the paper could result in serious thermal injury.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-05-22
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/c3a0c5ba-9d7a-4201-b748-d91e57220c4b