Med-Mizer, Inc.
Med-Mizer, Inc. has 3 FDA enforcement events on this register (6 product records) between 2014 and 2023: 3 device; the busiest year was 2014 with 1.
0% of its events are Class I; the most common class is Class II (3). 1 event is listed as ongoing; the recalling firm's address is in IN.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 3 Feb 2023 | Med-Riser MR600 Patient Lift | Device | Class II | 2 | Ongoing |
| 25 Jul 2018 | PR1000 Pivot Rehab Bed AC powered adjustable bed. | Device | Class II | 1 | Terminated |
| 18 Apr 2014 | RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 762 ( 76 " bed w/ 2 motors); 763 (3 motors); 763 A ( 3 motors, autocontour) 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care. | Device | Class II | 3 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Med-Mizer, Inc. had?
3 enforcement events (6 product records) on this register, 2014–2023: 3 device.
Are any Med-Mizer, Inc. recalls ongoing?
1 event is listed as ongoing in the current openFDA export.
What class are Med-Mizer, Inc. recalls?
3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.