Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 5490LOW
type: Dataset
description: FDA recall Z-1251-2024 — Invacare Corporation is recalling Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 5490LOW (Devices, Class II). The enforcement record is RECORDED; the classification is a DETERMINATION (FDA's regulatory verdict); the boundary is INTERPRETATION (a recall ≠ harm to a specific person). Source: openFDA. CC0.
license: https://creativecommons.org/publicdomain/zero/1.0/
is accessible for free: true
is part of: https://drug-device-safety-atlas.ryanjhunter.workers.dev/
is defined by: https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native
see also: https://agenticu.ryanjhunter.workers.dev/commons/the-research-object
date modified: 2026-06-24T07:02:03.626072+00:00
is based on: openFDA drug & device enforcement (recall) reports
  type: Dataset
  creator: U.S. Food & Drug Administration
about: Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 5490LOW
  type: MedicalDevice
  manufacturer: Invacare Corporation
claims: enforcement-record
claims: FDA classified recall Z-1251-2024 as Class II
claims: What an FDA recall is — and is NOT
has part: FDA recall details — Z-1251-2024
  type: ItemList
  number of items: 9
  item list element: ListItem
    position: 1
    item:
      field: Recall number
      value: Z-1251-2024
      status: recorded
  item list element: ListItem
    position: 2
    item:
      field: Product type
      value: Devices
      status: recorded
  item list element: ListItem
    position: 3
    item:
      field: Classification
      value: Class II
      status: determination
  item list element: ListItem
    position: 4
    item:
      field: Status
      value: Ongoing — the recall is still being carried out.
      status: recorded
  item list element: ListItem
    position: 5
    item:
      field: Recalling firm
      value: Invacare Corporation
      status: recorded
  item list element: ListItem
    position: 6
    item:
      field: Reason
      value: Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld failures to occur on these components
      status: recorded
  item list element: ListItem
    position: 7
    item:
      field: Initiated
      value: 2024-01-22
      status: recorded
  item list element: ListItem
    position: 8
    item:
      field: Lot/code info
      value: (1) G50 HEAD SECTION FULL ELECTRIC G-SERIES BED Serial Number 23HX000383 23HX000384 23HX000385 23HX000386 23HX000387 23HX000388 23HX000389 23HX000390 23HX000391 23HX000392 23HX000396 23HX000406 23HX000407 23HX000408 23HX000409 23HX000410 23HX000411 23HX000412 23HX000413 23HX000414 23HX000421 23HX000437 23HX000438 23HX000453 23HX000454 23HX000456 23HX000457 23HX000458 23HX000459 23HX000460 23HX000461 23HX000462 23HX000463 23HX000464 23HX000470 23HX000471 23HX000474 23HX000475 23HX000476 23HX000477 23HX000478 23HX000479 23HX000480 23HX000481 23HX000482 23HX000483 23HX000484 23HX000485 23HX000486 23HX000487 23HX000488 23HX000489 23HX000490 23HX000491 23HX000492 23HX000493 23HX000494 23HX000495 23HX000496 23HX000497 23HX000498 23HX000499 23HX000500 23HX000501 23HX000502 23HX000503 23HX000504 23HX000505 23HX000506 23HX000507 23HX000513 23HX000514 23HX000515 23HX000521 23HX000522 23HX000524 23HX000530 23HX000531 23HX000534 23HX000535 23HX000536 23HX000537 23HX000538 23HX000539 23HX000540 23HX000541 23HX000542 23HX000543 23HX000544 23HX000545 23HX000546 23HX000561 23HX000562 23HX000563 23HX000564 23HX000566 23HX000568 23HX000569 23HX000570 23HX000572 23HX000573 23HX000574 23HX000579 23HX000581 23HX000582 23HX000598 23HX000599 23HX000600 23HX000601 23HX000602 23HX000608 23HX000609 23HX000610 23HX000611 23HX000612 23HX000613 23HX000614 23HX000615 23HX000616 23HX000617 23HX000618 23HX000619 23HX000620 23HX000621 23HX000622 23HX000638 23HX000639 23HX000640 23HX000641 23HX000642 23HX000643 23HX000644 23HX000645 23HX000646 23HX000647 23HX000658 23HX000659 23HX000660 23HX000661 23HX000662 23HX000663 23HX000664 23HX000665 23HX000666 23HX000667 23HX000668 23HX000669 23HX000670 23HX000671 23HX000672 23HX000675 23HX000676 23HX000677 23HX000679 23HX000680 23HX000688 23HX000689 23HX000690 23HX000691 23HX000692 23HX000693 23HX000694 23HX000695 23HX000696 23HX000697 23HX000698 23HX000699 23HX000700 23HX000701 23HX000702 23HX000703 23HX000704 23HX000705 23HX000706 23HX000707 23HX000708 23…
      status: recorded
  item list element: ListItem
    position: 9
    item:
      field: Distribution pattern
      value: US Nationwide distribution.
      status: recorded

enforcement-record
type: Claim
name: FDA recall Z-1251-2024: Invacare Corporation is recalling Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 5490LOW
text: The FDA logged enforcement record Z-1251-2024: Invacare Corporation is voluntarily recalling Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 5490LOW — reason: Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld failures to occur on these components. Status: Ongoing — the recall is still being carried out.. Initiated 2024-01-22. Affected lots/codes: (1) G50 HEAD SECTION FULL ELECTRIC G-SERIES BED Serial Number 23HX000383 23HX000384 23HX000385 23HX000386 23HX000387 23HX000388 23HX000389 23HX000390 23HX000391 23HX000392 23HX000396 23HX000406 23HX000407 23HX000408 23HX000409 23HX000410 23HX000411 23HX000412 23HX000413 23HX000414 23HX000421 23HX000437 23HX000438 23HX000453 23HX000454 23HX000456 23HX000457 23HX000458 23HX000459 23HX000460 23HX000461 23HX000462 23HX000463 23HX000464 23HX000470 23HX000471 23HX000474 23HX000475 23HX000476 23HX000477 23HX000478 23HX000479 23HX000480 23HX000481 23HX000482 23HX000483 23HX000484 23HX000485 23HX000486 23HX000487 23HX000488 23HX000489 23HX000490 23HX000491 23HX000492 23HX000493 23HX000494 23HX000495 23HX000496 23HX000497 23HX000498 23HX000499 23HX000500 23HX000501 23HX000502 23HX000503 23HX000504 23HX000505 23HX000506 23HX000507 23HX000513 23HX000514 23HX000515 23HX000521 23HX000522 23HX000524 23HX000530 23HX000531 23HX000534 23HX000535 23HX000536 23HX000537 23HX000538 23HX000539 23HX000540 23HX000541 23HX000542 23HX000543 23HX000544 23HX000545 23HX000546 23HX000561 23HX000562 23HX000563 23HX000564 23HX000566 23HX000568 23HX000569 23HX000570 23HX000572 23HX000573 23HX000574 23HX000579 23HX000581 23HX000582 23HX000598 23HX000599 23HX000600 23HX000601 23HX000602 23HX000608 23HX000609 23HX000610 23HX000611 23HX000612 23HX000613 23HX000614 23HX000615 23HX000616 23HX000617 23HX000618 23HX000619 23HX000620 23HX000621 23HX000622 23HX000638 23HX000639 23HX0006…
claim type: official_fact
review status: current
commercial influence: false
epistemic status:
  occurred: true
  supported: true
  adjudged: true
  operative: true
grounding:
  grounding type: SourceCitation
  source: openFDA drug & device enforcement (recall) reports — U.S. FDA
  source url: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm
  value: Devices recall, status Ongoing
  adjudicator: openFDA drug & device enforcement (recall) reports — U.S. FDA
falsifier: A RECORD of measured/reported events (occurred=true) from openFDA drug & device enforcement (recall) reports — U.S. FDA; superseded when openFDA drug & device enforcement (recall) reports — U.S. FDA publishes its next release.

FDA classified recall Z-1251-2024 as Class II
type: Claim
text: The FDA assigned this recall Class II: Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.. This is the FDA's official risk classification — its regulatory DETERMINATION of the hazard category (a verdict constituted by the FDA's recognition, occurred=FALSE), adjudged=TRUE because the FDA issued it. It is NOT a measurement of harm to any specific person.
claim type: regulatory_determination
review status: current
commercial influence: false
epistemic status:
  occurred: false
  supported: true
  adjudged: true
  operative: true
grounding:
  grounding type: AdjudicativeAct
  source: U.S. FDA recall classification (openFDA enforcement)
  source url: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm
  value: Class II
  adjudicator: U.S. FDA recall classification (openFDA enforcement)
falsifier: occurred=FALSE: a regulatory DETERMINATION (an authority's classification/judgment) has NO material truthmaker independent of recognition — it is constituted by U.S. FDA recall classification (openFDA enforcement)'s say-so (a Searle institutional fact), not measured. adjudged=TRUE because U.S. FDA recall classification (openFDA enforcement) (an external authority) issued it. Distinct from a recorded measurement (which has an independent truthmaker) and from a modeled figure (a computed quantity, not a verdict). Challengeable; superseded if the authority reclassifies.

What an FDA recall is — and is NOT
type: Claim
text: A recall is a RECORDED FDA enforcement action — the FDA logged that a firm is removing or correcting a product, classed by the FDA's risk judgment. It does NOT establish that any specific unit is affected or caused harm; causation is not established. This record informs and compares — it is NOT medical advice and does not tell anyone to start or stop a drug or device. For a medical decision, route to the FDA recall record and a licensed pharmacist or prescriber.
claim type: interpretation
review status: current
commercial influence: false
epistemic status:
  occurred: false
  supported: true
  adjudged: false
  operative: true
grounding:
  grounding type: Interpretation
  source: Atlas Commons L5 boundary (enforcement-action ≠ harm causation)
  source url: https://drug-device-safety-atlas.ryanjhunter.workers.dev/
  value: a recorded enforcement action, not proof of harm or causation; not medical advice
falsifier: occurred=FALSE (a framing, not an event) and adjudged=FALSE (an in-house reading, not an authority's verdict) — the LOWEST-warrant claim here. A flat representation would render this identically to the official facts; the four-status does not.