Recall Z-1204-2023— Med-Mizer, Inc.
Class II · Ongoing
Class II FDA medical device recall by Med-Mizer, Inc., initiated 2023-02-03. FDA's recall record names no specific 510(k) clearance for this event. Product: Med-Riser MR600 Patient Lift. Reason: Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side..
- Recalling firm
- Med-Mizer, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-02-03
- Firm location
- Batesville, IN, United States
Product description
Med-Riser MR600 Patient Lift
Reason for recall
Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side.
Data sourced from openFDA. This site is unofficial and independent of the FDA.