Mequ M Warmer

MEQU M Warmer Recall Summary The MEQU M Warmer has been recalled and must be returned to the supplier. This product was distributed to hospitals, pharmacies, and laboratories in New Zealand. The recall is classified as Class I, which indicates a serious safety or quality concern.

Recalling firm
Oceania Medical Ltd
Product
MEQU M Warmer. [Device]. Model: M Warmer. Affected: Models - MWS201 (Box of 5), MWS201W (Single unit)
Reason
The manufacturer has identified a manufacturing defect involving incorrect sealing, which may cause internal leakage and overheating of the device., This may result in:, Activation of safety circuit (flashing red LED), Potential leakage of hot fluids, Risk of patient skin burns if undetected
Classification
Class I
Category
medical device recall
Country
New Zealand
Agency
MEDSAFE
Recall date
2026-04-16
Status
Ongoing
Distribution
New Zealand - Hospital/Pharmacy/Laboratory

Official recall notice from MEDSAFE

Recall details on Nibble Recalls: https://trynibble.app/recalls/415de565-95e2-449d-a64d-40a744e2a439