Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled,…
Medical device recall Z-2130-2023. Published in FDA’s Enforcement Report on Jul 19, 2023.
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 Jul 19, 2023. 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
- 1,980 cots 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?
Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty raising or lowering the cot, cot tip, or erratic or unintended motion.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is designed to support and transport a maximum weight of 700 lb (318 kg). Model Number: 6507
1,980 cots, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Model: 650700000000 UDI-DI: 07613327504460; Model: 650705550001 UDI-DI: 07613327559118; Model: 650705550002 UDI-DI: 07613327559125; Cots shipped between February 11, 2022 and February 1, 2023 Serial Numbers: 2112001485 2112001488…
Every code shown here, 1,990 characters
Model: 650700000000 UDI-DI: 07613327504460; Model: 650705550001 UDI-DI: 07613327559118; Model: 650705550002 UDI-DI: 07613327559125; Cots shipped between February 11, 2022 and February 1, 2023 Serial Numbers: 2112001485 2112001488 2112001489 2112001490 2112001491 2112001492 2112001493 2112001494 2112001495 2112001496 2112001501 2112001503 2112001504 2112001508 2112001509 2112001510 2112001511 2112001512 2112001513 2112001514 2112001515 2112001516 2112001517 2112001518 2112001519 2112001520 2112001521 2112001522 2112001523 2112001524 2112001525 2112001526 2112001527 2112001528 2112001529 2112001530 2112001531 2112001532 2112001533 2112001534 2112001535 2112001536 2202000473 2202000474 2202000475 2202000476 2202000477 2202000478 2202000479 2202000480 2202000481 2202000482 2202000483 2202000484 2202000485 2202000487 2202000488 2202000489 2202000490 2202000491 2202000492 2202000797 2202000798 2202000799 2202000800 2202000801 2202000802 2202000803 2202000804 2202000805 2202000806 2202000807 2202000808 2202000809 2202000810 2202000811 2202000812 2202000813 2202000814 2202000815 2202000816 2202000817 2202000819 2202000820 2202000821 2202000822 2202000823 2202000824 2202000825 2202000826 2202001299 2202001300 2202001301 2202001302 2202001303 2202001304 2202001305 2202001306 2202001307 2202001308 2202001309 2202001311 2202001312 2202001313 2202001314 2202001315 2202001316 2202001317 2202001318 2202001518 2202001519 2202001520 2202001521 2202001522 2202001523 2202001524 2202001526 2202001535 2202001539 2202001541 2202001544 2202001545 2202001546 2202001547 2202001548 2202001549 2202001552 2202001554 2202001555 2202001556 2202001557 2202001558 2202001560 2202001561 2202001562 2202001563 2202001564 2202001565 2202001566 2202001568 2202001569 2202001570 2202001572 2202001573 2202001574 2202001575 2202001576 2202001577 2202001578 2202001579 2202001580 2202001582 2202001584 2202001585 2202001587 2202001590 2202001591 2202001592 2202001593 2202001594 2202001597 2202001795…
FDA’s list runs to 21,988 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.
Worldwide distribution - US Nationwide and the countries of Australia, Canada, Netherlands, Switzerland, United Kingdom.
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.
The words say it went outside the United States too.
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 May 24, 2023.
- FDA classified it on Jul 12, 2023.
- FDA’s Enforcement Report published it on Jul 19, 2023.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Stryker Medical Division of Stryker Corporation, of Portage, MI.
- 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 21,988 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.