Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated…
Medical device recall Z-1468-2025. Published in FDA’s Enforcement Report on Apr 2, 2025.
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 2, 2025. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 2,126 units 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?
The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, and P7520A4S.
2,126 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
P7520A19 UDI-DI: 00887761999893; P7520A20S UDI-DI: 00887761999886; P7520A21 UDI-DI: 00887761999879; P7520A22S UDI-DI: 00887761999862; P7520A23 UDI-DI: 00887761999855; P7520A24S UDI-DI: 00887761999848; P7520A3 UDI-DI: 00887761999770;…
Every code shown here, 1,998 characters
P7520A19 UDI-DI: 00887761999893; P7520A20S UDI-DI: 00887761999886; P7520A21 UDI-DI: 00887761999879; P7520A22S UDI-DI: 00887761999862; P7520A23 UDI-DI: 00887761999855; P7520A24S UDI-DI: 00887761999848; P7520A3 UDI-DI: 00887761999770; P7520A31 UDI-DI: 00887761999756; P7520A37 UDI-DI: 00887761999718; P7520A39 UDI-DI: 00887761999701; P7520A45 UDI-DI: 00887761999671; P7520A4S UDI-DI: 00887761999657; Serial Numbers: A008MW1489 Y298MW1411 Y298MW1412 Y298MW1413 Y298MW1414 Y298MW1415 Y298MW1416 Y298MW1417 Y298MW1418 Y298MW1419 Y298MW1420 Y298MW1421 Y298MW1452 Y298MW1453 Y298MW1454 Y298MW1455 Y298MW1456 Y298MW1457 Y298MW1458 Y298MW1459 Y298MW1460 Y298MW1461 Y298MW1463 Y298MW1464 Y298MW1465 Y298MW1466 Y298MW1467 Y298MW1468 Y298MW1469 Y298MW1470 Y298MW1471 Y298MW1472 Y298MW1473 Y298MW1474 Y298MW1475 Y298MW1580 Y298MW1581 Y298MW1582 Y298MW1583 Y298MW1584 Y298MW1585 Y298MW1586 Y298MW1587 Y298MW1588 Y298MW1589 Y298MW1590 Y298MW1591 Y298MW1592 Y298MW1593 Y298MW1594 Y298MW1595 Y298MW1596 Y298MW1597 Y298MW1598 Y298MW1599 Y298MW1600 Y298MW1601 Y298MW1602 Y298MW1603 Y298MW1604 Y298MW1605 Y298MW1606 Y298MW1607 Y298MW1608 Y298MW1609 Y298MW1610 Y298MW1611 Y298MW1612 Y298MW1613 Y298MW1614 Y298MW1615 Y298MW1616 Y298MW1617 Y298MW1618 Y298MW1619 Y298MW1620 Y298MW1621 Y298MW1622 Y298MW1623 Y303MW2164 Y303MW2165 Y303MW2166 Y303MW2167 Y303MW2168 Y303MW2169 Y303MW2170 Y303MW2171 Y305MW2526 Y305MW2527 Y305MW2528 Y305MW2529 Y305MW2530 Y305MW2531 Y305MW2532 Y305MW2533 Y306MW2730 Y306MW2731 Y306MW2732 Y306MW2733 Y306MW2734 Y306MW2735 Y306MW2736 Y306MW2737 Y306MW2738 Y306MW2739 Y306MW2844 Y306MW2845 Y306MW2846 Y306MW2847 Y306MW2848 Y306MW2849 Y306MW2850 Y306MW2851 Y306MW2852 Y306MW2853 Y306MW2854 Y306MW2855 Y306MW2856 Y306MW2857 Y306MW2858 Y312MW3805 Y312MW3806 Y312MW3807 Y312MW3808 Y312MW3809 Y312MW3810 Y312MW3811 Y312MW3812 Y312MW3813 Y312MW3814 Y312MW3815 Y312MW3816 Y312MW3817 Y312MW3818 Y312MW3819 Y312MW3820 Y312MW3821 Y312MW3822 Y312MW3823 Y312MW3824 Y312MW3825 Y314MW4237 Y314MW4238 Y314MW4239…
FDA’s list runs to 27,044 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.
US Nationwide. Global Distribution.
These words name no state.
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?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, 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 Feb 25, 2025.
- FDA classified it on Mar 26, 2025.
- FDA’s Enforcement Report published it on Apr 2, 2025.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Baxter Healthcare Corporation, of Deerfield, IL.
- 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 27,044 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
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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.