Recall archive / FDA device enforcement
Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS — FDA record Z-1239-2022
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
- Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS
- Reason
- The 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
- 109
- Agency-reported status
- Terminated
- Source record identifier
- Z-1239-2022
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: n/a Serial Numbers: PWK769356 PWK769357 PWK769358 PWK769359 PWK769360 PWK769361 PWK769362 PWK769363 PWK769364 PWK769365 PWK769366 PWK769367 PWK769368 PWK769369 PWK769370 PWK769371 PWK769372 PWK769373 PWK769374 PWK769375 PWK769376 PWK769377 PWK769378 PWK769379 PWK769380 PWK769381 PWK769382 PWK769383 PWK769384 PWK769385 PWK769386 PWK769387 PWK769388 PWK769389 PWK769390 PWK769391 PWK769392 PWK769393 PWK769394 PWK769395 PWK769396 PWK769397 PWK769398 PWK769399 PWK769400 PWK769401 PWK769402 PWK769403 PWK769404 PWK769405 PWK769406 PWK769407 PWK769408 PWK769409 PWK769410 PWK769411 PWK769412 PWK769413 PWK769414 PWK769415 PWK769416 PWK769417 PWK769418 PWK769419 PWK769420 PWK769421 PWK769422 PWK769423 PWK769424 PWK769425 PWK769426 PWK769427 PWK769428 PWK769429 PWK769430 PWK769431 PWK769432 PWK769433 PWK769434 PWK769435 PWK769436 PWK769437 PWK769438 PWK769439 PWK769440 PWK769441 PWK769442 PWK769443 PWK769444 PWK769445 PWK769446 PWK769447 PWK769448 PWK769449 PWK769450 PWK769451 PWK769452 PWK769453 PWK769454 PWK769455 PWK769456 PWK769457 PWK769458 PWK769459 PWK769460 PWK769461 PWK769462 PWK769463 PWK769464 |
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.