Handicare Usa recalls
Handicare Usa has 5 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 29 Aug 2018. The most frequent reason is device malfunction.
Total recalls5since 2015
Last 12 months0reported
Class I00% of total
Ongoing0latest 29 Aug 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 5 100%Class III 0 0%
Why handicare usa is recalled
Product types
By year
All handicare usa recalls, newest first
5 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Handicare P600 Series Patient Lift recalled | Handicare Usa | Device Malfunction | Nationwide |
| Device | CLASS II | Handicare C Series Patient Lift recalled | Handicare Usa | Device Malfunction | Nationwide |
| Device | CLASS II | Prism Medical A-625, Max recalled by Handicare Usa | Handicare Usa | Other | MO |
| Device | CLASS II | ReTurn 7500/7500 Aid, transfer recalled by Handicare USA | Handicare USA | Other | 8 states |
| Device | CLASS II | ReTurn belt, wipeable, sizes Small through Extra Large recalled | Handicare USA | Foreign Material | 5 states |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.