Oakworks Bed (Emergency Field Bed)
Medical device recall Z-1239-2022. Published in FDA’s Enforcement Report on Jun 15, 2022.
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 Jun 15, 2022. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 3 states named
- 109 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?
The warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS
109, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
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…
Every code shown here, 1,117 characters
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
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.
US Nationwide distribution in the states of MA, NJ, and PA.
The states and territories these words name
- Massachusetts
- New Jersey
- Pennsylvania
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.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, 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 Apr 21, 2022.
- FDA classified it on Jun 6, 2022.
- FDA’s Enforcement Report published it on Jun 15, 2022.
- FDA terminated it on Sep 19, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Oakworks Inc, of New Freedom, PA.
- 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.”
- 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
-
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.