Drop Hooks for Xact (tm) Lo-Pro with Removeable Drop Seat, Xact Integrated, and Xact Individual with Integrated Drop Sea
FDA device recall Z-316/318-3 · posted 2002-12-05 · Terminated
Recall details
- Recalling firm
- Action Products Incorporated
- Reason for recall
- Wheelchair seat component is defective.
- Action taken
- Firm notified customers by certified letter 5/14/02 and advised of potential for serious injury. Letter instructs customers to cease use and distribution of any defective hooks and return for replacement. Firm additonally instructed dealers to notify end-users about the recall.
- Root cause
- Other
- Status
- Terminated
- Product code
- KNO
- Quantity affected
- 73 sets
- Distribution
- Product was sold to medical supply firms in LA, IN, and MA and to international customers.
- Date initiated
- 2002-05-14
- Date posted
- 2002-12-05
- Date terminated
- 2002-12-10
- Location
- Hagerstown, MD
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.