Recall Z-0441-2019— R82 A/S
Class II · Ongoing
Class II FDA medical device recall by R82 A/S, initiated 2017-06-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Heron toilet and bath chair Model 880505-01 & 880505-11. Reason: Replacement campaign on all units that have a gas spring head in aluminum..
- Recalling firm
- R82 A/S
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2017-06-30
- Firm location
- Gedved, Denmark
Product description
Heron toilet and bath chair Model 880505-01 & 880505-11
Reason for recall
Replacement campaign on all units that have a gas spring head in aluminum.
Data sourced from openFDA. This site is unofficial and independent of the FDA.