400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 lb 400600 Scale Hanger Assembly Product Usage:…
Medical device recall Z-1450-2014. Published in FDA’s Enforcement Report on Apr 16, 2014.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Apr 16, 2014. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 24 states named
- 514 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
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.
514, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Serial # 0810LS1522 0810LS1523 0910LS1524 0910LS1525 0910LS1526 0910LS1527 0910LS1528 0804LS0854 0910LS1529 0910LS1530 1010LS1532 0910LS1531 1010LS1533 1010LS1534 1010LS1535 1010LS1536 1010LS1537 1010LS1538 1010LS1539 1010LS1540 1010LS1541…
Every code shown here, 1,990 characters
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 1211LS1668 1211LS1669 1211LS1670 1211LS1671 1211LS1672 1211LS1673 1211LS1674 1211LS1678 0112LS1683 0112LS1681 0112LS1682 0112LS1684 1211LS1675 1211LS1676 1211LS1677 0112LS1680 0112LS1685 0911LS1635 1211LS1679 0112LS1686 0112LS1687 0112LS1688 0112LS1689 0112LS1690 0112LS1691 0212LS1693 0212LS1694 0212LS1692 0212LS1697 0212LS1698 0212LS1699 0212LS1700…
FDA’s list runs to 5,159 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
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.
The states and territories these words name
24 states and territories.
Every one of them
- California
- Colorado
- Iowa
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Maryland
- Maine
- Michigan
- Minnesota
- Mississippi
- North Dakota
- Nebraska
- New Hampshire
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- South Dakota
- Texas
- Wisconsin
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on May 10, 2013.
- FDA classified it on Apr 10, 2014.
- FDA’s Enforcement Report published it on Apr 16, 2014.
- FDA terminated it on Nov 20, 2014.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- ErgoSafe Product LLC dba Prism Medical Services, of Toronto, ON, Canada.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 5,159 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.