Recall Register

Food, drugs, devices › Firms

Handicare Usa Inc

FDA recalling firm · 4 enforcement events · 5 product records · 2014–2017 · MO, PA

Handicare Usa Inc has 4 FDA enforcement events on this register (5 product records) between 2014 and 2017: 4 device; the busiest year was 2017 with 2.

0% of its events are Class I; the most common class is Class II (4). 0 events are listed as ongoing; the recalling firm's address is in MO and PA.

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

InitiatedProduct (first record)TypeClassRecordsStatus
3 Nov 2017Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.DeviceClass II2Terminated
8 Sep 2017PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C poweredDeviceClass II1Terminated
26 Mar 2015ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch. Patient transfer aid.DeviceClass II1Terminated
15 Apr 2014ReTurn 7500/7500 Aid, transferDeviceClass II1Terminated

By type and class

Device4
Class II4

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

14
16
18
20
22
24
26
Enforcement events for Handicare Usa Inc by year initiated.

Questions and answers

How many FDA recalls has Handicare Usa Inc had?

4 enforcement events (5 product records) on this register, 2014–2017: 4 device.

Are any Handicare Usa Inc recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Handicare Usa Inc recalls?

4 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.