Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
Medical device recall Z-2179-2017. Published in FDA’s Enforcement Report on Jun 7, 2017.
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 7, 2017. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 2 states named
- 2,380 (2,215 US; 165 OUS) 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?
Reported incidents of a patient step detaching from the table. A fall from a patient step detaching while in use could result in an injury to a patient or operator.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
2,380 (2,215 US; 165 OUS), in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
FMI 10908 Initial Consignee List Mfg. Lot or Serial # System ID 00000959002WK7 907276RM4 00000966338WK6 256235ORF1 00000966611WK6 256235ORF2 00000956387WK5 205783LRF2 00000525674WK8 205793FR1 00000964963WK3 205387LRF 964349WK5 334732SRF…
Every code shown here, 1,994 characters
FMI 10908 Initial Consignee List Mfg. Lot or Serial # System ID 00000959002WK7 907276RM4 00000966338WK6 256235ORF1 00000966611WK6 256235ORF2 00000956387WK5 205783LRF2 00000525674WK8 205793FR1 00000964963WK3 205387LRF 964349WK5 334732SRF 00000969028WK0 205345RF3 952032WK1 501968LEG 00000510900WK4 501863MLEG 00000277058TU4 479441RF1 00000974520WK9 501321LEG1 29415VP7 928763RF 00000543656WK3 602856LEG 00000551387WK4 602994DRS 984281WK6 928537RM1 00000983374WK0 928537RM2 00000960138WK6 209386ATWRF 00000130329TX6 RADNETRF119 00000546581WK0 650696M6 00000978807WK6 818884LRF1 00000023282M37 RADNETRF1260 00000499668WK2 818331SFX 538693WK3 RADNETRF118 00000972384WK2 RADNETRF144 00000962460WK2 RADNETRF130 00000980889WK0 RADNETRF193 00000530446WK4 209225LEG2 00000531588WK2 209225LEG3 00000517706WK8 510370RFDG1 00000518141WK7 510370RFDG2 00000968783WK1 RADNETRF138 00000963491WK6 RADNETRF137 00000961786WK1 925370LMRF1 00000973156WK3 RADNETRF146 00000953812WK5 RADNETRF126 00000522090WK0 760446RC1 00000969297WK1 909788LF3 00000967126WK4 909788LF4 1025367WK2 RADNETRF129 00000978314WK3 916784LEG 00000978316WK8 619543RF4 00000975431WK8 619543RF5 00000974139WK8 415923LEGACYGI 00000547501WK7 415923PR5 00000963305WK8 408977RF5 00000552931WK8 RADNETRF122 00000966068WK9 RADNETRF139 00001005270WK2 RADNETRF143 00000523402WK6 707462ULEGACY 00000972383WK4 303440BCHRM4 986114WK7 303440LEG1 986513WK0 303355RF 00000503355WK0 970945RM2 00000959073WK8 303CMCRM1 00000954518WK7 719556RM1 00000977456WK3 203331RF1 00000507625WK2 203785RF1 972381WK8 860350RF1 00000543348WK7 703697RF2 00000967162WK9 302392RF 00000961102WK1 302654RF 00000549578WK3 407830RF4 00000956746WK2 561965RM1 00000957833WK7 561965RM3 00000958809WK6 561965RM4 00000538300WK5 305682RM5 546369WK0 305AHLEG2 00000549923WK1 863533RM1 00000963738WK0 941798RM2 00000981461WK7 941798RM3 00000516439WK7 813681RM3 00000519515WK1 813681SPEC1 00000518140WK9 407566CH2 00000979197WK1 239432RF1 00000969627WK9 239931RM2 00000955947WK7 941437RF1…
FDA’s list runs to 60,590 characters. The first part is shown; the rest is on FDA’s record.
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 including DC and Puerto Rico. OUS: Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Egypt, France, Germany, Greece, Honduras, Hungary, Indonesia, Ireland, Israel, Italy, Jamaica, Jordan, Kuwait, Libya, Malaysia, Malta, Mexico, Panama, Portugal, Russia, Saudi Arabia, Saudi Arabia, Slovakia, Spain, Thailand, United Arab Emirates, United Kingdom, Vietnam.
The states and territories these words name
- District of Columbia
- Puerto Rico
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.
The words say it went outside the United States too.
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 Feb 6, 2017.
- FDA classified it on May 31, 2017.
- FDA’s Enforcement Report published it on Jun 7, 2017.
- FDA terminated it on Mar 2, 2018.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- GE Healthcare, LLC, of Waukesha, WI.
- 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.”
- FDA’s list of codes runs to 60,590 characters; the first part is shown here, and the rest is on FDA’s record.
- 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.