Recall Z-2470-2021— Getinge Dominican Republic SA
Class II · Terminated
Class II FDA medical device recall by Getinge Dominican Republic SA, initiated 2021-07-30, terminated 2023-08-11. FDA's recall record names no specific 510(k) clearance for this event. Product: Arjo Disposable Repositioning Sling, Model AHD001. Reason: Sling loop straps on device pose a trip hazard..
- Recalling firm
- Getinge Dominican Republic SA
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-07-30
- Terminated
- 2023-08-11
- Firm location
- Itabo, Haina, N/A, Dominican Republic (the)
Product description
Arjo Disposable Repositioning Sling, Model AHD001
Reason for recall
Sling loop straps on device pose a trip hazard.
Data sourced from openFDA. This site is unofficial and independent of the FDA.