FDAFDA · Food and drugs·Recall number Z-1450-2014
400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 lb 400600 Scale Hanger Assembly Product Usage: The intended use is a patient hanger bar (400600) attached to a 400003 or 400013 floor lift used to lift, transfer or position clients.
Published April 16, 2014 · Recall initiated: May 10, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
MedCare Products has determined that a number of their Floor Lifts manufactured from 9/1/2010 to 11/7/2012 do not meet MedCare's high standards. The original design includes a pin that over time and years of use may stop performing as designed and may break.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- ErgoSafe Product LLC dba Prism Medical Services
- Distributor
- USA Nationwide Distribution in the states of: CA, CO, IL, IN, IA, KS, KY, LA, ME, MD, MI, MN, MS, NO, NE,NH,NY, ND,OH, OK, OR, PA , SD, TX, WI.
- Lot
- Serial # 0810LS1522 0810LS1523 0910LS1524 0910LS1525 0910LS1526 0910LS1527 0910LS1528 0804LS0854 0910LS1529 0910LS1530 1010LS1532 0910LS1531 1010LS1533 1010LS1534 1010LS1535 1010LS1536 1010LS1537 1010LS1538 1010LS1539 1010LS1540 1010LS1541 1010LS1542 1010LS1543 1010LS1544 1010LS1545 1010LS1546 1010LS1547 1010LS1548 1110LS1549 1201LS1551 1210LS1550 1210LS1552 1210LS1553 1210LS1554 1210LS1555 1210LS1556 1210LS1557 0111LS1558 0111LS1561 0111LS1560 0111LS1562 0111LS1563 0111LS1564 0111LS1565 0111LS1566 0111LS1567 0111LS1559 0111LS51559 0111LS1568 0211LS1569 0211LS1570 0211LS1571 0211LS1572 0311LS1573 0311LS1575 0311LS1576 0311LS1578 0311LS1577 0311LS1579 0311LS1580 0311LS1583 0311LS1581 0311LS1582 0311LS1586 0311LS1574 0311LS1585 0311LS1587 0411LS1588 0411LS1589 0411LS1590 0411LS1591 0411LS1592 0411LS1593 0411LS1594 0511LS1597 0511LS1598 0511LS1599 0511LS1596 0511LS1600 0511LS1601 0511LS1602 0411LS1595 0511LS1603 0611LS1605 0611LS1604 0611LS1606 0611LS1607 0611LS1608 0611LS1609 0611LS1610 0611LS1611 0711LS1612 0711LS1613 0711LS1614 0711LS1615 0711LS1616 0711LS1617 0711LS1618 0711LS1619 0711LS1620 0311LS1584 0711LS1621 0711LS1622 0711LS1623 0811LS1624 0711LS1625 0811LS1625 0811LS1626 0811LS1627 0811LS1628 0811LS1629 0811LS1631 0811LS1630 0911LS1632 0911LS1633 0911LS1639 0911LS1636 0911LS1641 0911LS1642 0911LS1643 0911LS1644 0911LS1634 0911LS1637 0911LS1638 0911LS1640 0911LS1645 1011LS1647 1011LS1646 1011LS1648 1011LS1649 1011LS1650 1011LS1651 1011LS1652 1011LS1653 1011LS1655 1011LS1654 1011LS1656 1011LS1658 1011LS1657 1011LS1659 1011LS1660 1211LS1661 1211LS1662 1211LS1663 1211LS1664 1211LS1665 1211LS1666 1211LS1667
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Canada
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