Lower riskMedical device recall · FDA · Published April 21, 2022
Oakworks PX200 Emergency Bed Recall: Incorrect Weight Label (400 lbs vs 500 lbs)
Oakworks recalls PX200 Emergency Relief Beds with incorrect weight capacity labels (stating 500 lbs when it should be 400 lbs). Affected units have specific serial numbers. Contact Oakworks for replacement.
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.
Take action
Contact the company
📍Recalling firmOakworks Inc923 E Wellspring Rd · New Freedom, PA 17349-8408
“Oakworks PX200 Emergency Bed Recall: Incorrect Weight Label (400 lbs vs 500 lbs).” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60784-oakworks-px200-emergency-bed-recall-incorrect-weight-label-400-lbs. Based on FDA recall #Z-1238-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1238-2022%22&limit=1).
The FDA announced on April 21, 2022, that Oakworks Inc recalled PX200 Emergency Relief Beds because labels lacked UDI numbers and showed an incorrect weight capacity. Owners should contact the company for a remedy.
How to tell if you have it
Brand: Oakworks
Product: PX200 Emergency Relief Bed
Model No.: PXEXEB362280A6TTZZH4C19
UDI-DI: 00817463026399
Serial Numbers: PXR769629 through PXR769829 (specifically listed in record)
Distribution: US Nationwide, including MA, NJ, and PA
The hazard
The product label was printed without the UDI number and the warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.
Context
GovInfoNow's records show Oakworks Inc has had four other recalls since July 31, 2017. On December 5, 2023, the company recalled ultrasound tables due to backrest fracture risks when inclined. A June 29, 2021 recall involved vascular tables with weld failure risks causing tilting malfunctions. Other recent recalls of similar products include Baxter Healthcare PRO+ 40" MRS SURFACE Mattress Recall (August 18, 2026).
How to tell if you have this one
Check the serial numbers on the bed: PXR769629 through PXR769829. The product label shows a weight capacity of 500 lbs instead of 400 lbs.
Brand
Oakworks
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
US Nationwide distribution in the states of MA, NJ, and PA.
Look for the serial numbers on the bed: PXR769629 through PXR769829.
Verify Weight Label
Confirm the weight capacity label states 500 lbs instead of the correct 400 lbs.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 3 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of MA, NJ, and PA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Massachusetts, New Jersey, Pennsylvania.
Recall timeline
FDA terminated this recall 2.4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1238-2022 (April 21, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1238-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.