Recall archive / FDA device enforcement
PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19 — FDA record Z-1238-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Apr 21, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19
- Reason
- Product label was printed without the UDI number and warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.
- Classification
- Class II
- Recalling firm
- Oakworks Inc
- Quantity
- 130
- Agency-reported status
- Terminated
- Source record identifier
- Z-1238-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: 00817463026399 Serial Numbers: PXR769629 PXR769630 PXR769631 PXR769632 PXR769633 PXR769634 PXR769635 PXR769636 PXR769637 PXR769638 PXR769639 PXR769640 PXR769641 PXR769642 PXR769643 PXR769644 PXR769645 PXR769646 PXR769647 PXR769648 PXR769649 PXR769650 PXR769651 PXR769652 PXR769653 PXR769654 PXR769655 PXR769656 PXR769657 PXR769658 PXR769730 PXR769731 PXR769732 PXR769733 PXR769734 PXR769735 PXR769736 PXR769737 PXR769738 PXR769739 PXR769740 PXR769741 PXR769742 PXR769743 PXR769744 PXR769745 PXR769746 PXR769747 PXR769748 PXR769749 PXR769750 PXR769751 PXR769752 PXR769753 PXR769754 PXR769755 PXR769756 PXR769757 PXR769758 PXR769759 PXR769760 PXR769761 PXR769762 PXR769763 PXR769764 PXR769765 PXR769766 PXR769767 PXR769768 PXR769769 PXR769770 PXR769771 PXR769772 PXR769773 PXR769774 PXR769775 PXR769776 PXR769777 PXR769778 PXR769779 PXR769780 PXR769781 PXR769782 PXR769783 PXR769784 PXR769785 PXR769786 PXR769787 PXR769788 PXR769789 PXR769790 PXR769791 PXR769792 PXR769793 PXR769794 PXR769795 PXR769796 PXR769797 PXR769798 PXR769799 PXR769800 PXR769801 PXR769802 PXR769803 PXR769804 PXR769805 PXR769806 PXR769807 PXR769808 PXR769809 PXR769810 PXR769811 PXR769812 PXR769813 PXR769814 PXR769815 PXR769816 PXR769817 PXR769818 PXR769819 PXR769820 PXR769821 PXR769822 PXR769823 PXR769824 PXR769825 PXR769826 PXR769827 PXR769828 PXR769829 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US Nationwide distribution in the states of MA, NJ, and PA.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Jun 15, 2022
- Recall initiation date
- Apr 21, 2022
- Center classification date
- Jun 6, 2022
- Termination date
- Sep 19, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.