Permobil, Ab recalls
Permobil, Ab has 3 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 26 Sep 2018. The most frequent reason is device malfunction.
Total recalls3since 2017
Last 12 months0reported
Class I00% of total
Ongoing0latest 26 Sep 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why permobil, ab is recalled
Product types
By year
All permobil, ab recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Permobil powered wheelchairs recalled by Permobil, Ab | Permobil, Ab | Device Malfunction | Nationwide |
| Device | CLASS II | Electric Wheelchairs: a) C300 Corpus II b) C350 Corpus II recalled | Permobil, Ab | Device Malfunction | Nationwide |
| Device | CLASS II | Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500 recalled | Permobil, Ab | Device Malfunction | Nationwide |
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.