CLASS II ONGOING Device recall · Reported 25 Dec 2024 · FDA Enforcement Report
OEC 3D recalled by GE OEC Medical Systems
GE OEC Medical Systems is recalling OEC 3D, distributed in 44 states. The recall was initiated on 21 Nov 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0703-2025
- FDA event ID
- 95846
- Recalling firm
- GE OEC Medical Systems, Salt Lake City, UT
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 21 Nov 2024
- FDA classified
- 18 Dec 2024
- Reported
- 25 Dec 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Device type
- Surgical Instruments
Timeline
| 21 Nov 2024 | Recall initiated by company | |
| 18 Dec 2024 | Classified by FDA | +27 days |
| 25 Dec 2024 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging system used to assist trained surgeons and other qualified physicians. The system is used to provide fluoroscopic Xray images and volumetric reconstructions during diagnostic, interventional, and surgical procedures.
Where it was distributed
U.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. O.U.S.: Australia, Brazil, Canada, Chile, Costa Rica, India, Italy, Philippines, Poland, Portugal, Sweden, Switzerland, and United Kingdom
AlaskaArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMarylandMichiganMinnesotaMissouri
Questions about this recall
Why was it recalled?
Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability.
Which lots are affected?
Product Name: OEC 3D GTIN code: 00195278096944 Lot/Serial Numbers / UDI codes: FBMHDX00436 (01)00195278096944(11)240800(21)FBMHDX00436 FBMHDX00352 (01)00195278096944(11)240500(21)FBMHDX00352 FBMHDX00455 (01)00195278096944(11)240900(21)FBMHDX00455 FBMHDX00384 (01)00195278096944(11)240600(21)FBMHDX00384 FBMHDX00434 (01)00195278096944(11)240900(21)FBMHDX00434 FBMHDX00443 (01)00195278096944(11)240900(21)FBMHDX00443 FBMHDX00407 (01)00195278096944(11)240700(21)FBMHDX00407 FBMHDX00363 (01)00195278096944(11)240500(21)FBMHDX00363 FBMHDX00424 (01)00195278096944(11)240800(21)FBMHDX00424 FBMHDX00442 (01)00195278096944(11)240900(21)FBMHDX00442 FBMHDX00321 (01)00195278096944(11)240300(21)FBMHDX00321 FBMHDX00387 (01)00195278096944(11)240600(21)FBMHDX00387 FBMHDX00339 (01)00195278096944(11)240400(21)FBMHDX00339 FBMHDX00448 (01)00195278096944(11)240900(21)FBMHDX00448 FBMHDX00383 (01)00195278096944(11)240600(21)FBMHDX00383 FBMHDX00437 (01)00195278096944(11)240900(21)FBMHDX00437 FBMHDX00362 (01)00195278096944(11)240500(21)FBMHDX00362 FBMHDX00394 (01)00195278096944(11)240600(21)FBMHDX00394 FBMHDX00397 (01)00195278096944(11)240700(21)FBMHDX00397 FBMHDX00395 (01)00195278096944(11)240700(21)FBMHDX00395 FBMHDX00355 (01)00195278096944(11)240500(21)FBMHDX00355 FBMHDX00374 (01)00195278096944(11)240600(21)FBMHDX00374 FBMHDX00451 (01)00195278096944(11)240900(21)FBMHDX00451 FBMHDX00368 (01)00195278096944(11)240500(21)FBMHDX00368 FBMHDX00457 (01)00195278096944(11)241000(21)FBMHDX00457 FBMHDX00440 (01)00195278096944(11)240900(21)FBMHDX00440 FBMHDX00419 (01)00195278096944(11)240800(21)FBMHDX00419 FBMHDX00421 (01)00195278096944(11)240800(21)FBMHDX00421 FBMHDX00427 (01)00195278096944(11)240800(21)FBMHDX00427 FBMHDX00459 (01)00195278096944(11)240900(21)FBMHDX00459 FBMHDX00378 (01)00195278096944(11)240600(21)FBMHDX00378 FBMHDX00345 (01)00195278096944(11)240400(21)FBMHDX00345 FBMHDX00458 (01)00195278096944(11)240900(21)FBMHDX00458 FBMHDX00425 (01)00195278096944(11)240800(21)FBMHDX00425 FBMHDX00366 (01)00195278096944(11)240500(21)FBMHDX00366 FBMHDX00480 (01)00195278096944(11)241100(21)FBMHDX00480 FBMHDX00418 (01)00195278096944(11)240800(21)FBMHDX00418 FBMHDX00454 (01)00195278096944(11)240900(21)FBMHDX00454 FBMHDX00188 (01)00195278096944(11)230300(21)FBMHDX00188 FBMHDX00403 (01)00195278096944(11)240700(21)FBMHDX00403 FBMHDX00452 (01)00195278096944(11)240900(21)FBMHDX00452 FBMHDX00386 (01)00195278096944(11)240600(21)FBMHDX00386 FBMHDX00343 (01)00195278096944(11)240400(21)FBMHDX00343 FBMHDX00369 (01)00195278096944(11)240500(21)FBMHDX00369 FBMHDX00464 (01)00195278096944(11)240900(21)FBMHDX00464 FBMHDX00413 (01)00195278096944(11)240800(21)FBMHDX00413 FBMHDX00346 (01)00195278096944(11)240400(21)FBMHDX00346 FBMHDX00388 (01)00195278096944(11)240600(21)FBMHDX00388 FBMHDX00389 (01)00195278096944(11)240600(21)FBMHDX00389 FBMHDX00406 (01)00195278096944(11)240700(21)FBMHDX00406 FBMHDX00416 (01)00195278096944(11)240800(21)FBMHDX00416 FBMHDX00453 (01)00195278096944(11)240900(21)FBMHDX00453 FBMHDX00399 (01)00195278096944(11)240700(21)FBMHDX00399 FBMHDX00401 (01)00195278096944(11)240700(21)FBMHDX00401 FBMHDX00428 (01)00195278096944(11)240800(21)FBMHDX00428 FBMHDX00380 (01)00195278096944(11)240600(21)FBMHDX00380 FBMHDX00371 (01)00195278096944(11)240600(21)FBMHDX00371 FBMHDX00392 (01)00195278096944(11)240600(21)FBMHDX00392 FBMHDX00344 (01)00195278096944(11)240400(21)FBMHDX00344 FBMHDX00404 (01)00195278096944(11)240700(21)FBMHDX00404 FBMHDX00356 (01)00195278096944(11)240500(21)FBMHDX00356 FBMHDX00376 (01)00195278096944(11)240600(21)FBMHDX00376 FBMHDX00470 (01)00195278096944(11)241000(21)FBMHDX00470 FBMHDX00353 (01)00195278096944(11)240500(21)FBMHDX00353 FBMHDX00359 (01)00195278096944(11)240500(21)FBMHDX00359 FBMHDX00391 (01)00195278096944(11)240600(21)FBMHDX00391 FBMHDX00460 (01)00195278096944(11)240900(21)FBMHDX00460 FBMHDX00410 (01)00840682121729(11)240700(21)FBMHDX00410 FBMHDX00379 (01)00195278096944(11)240600(21)FBMHDX00379 FBMHDX00390 (01)00195278096944(11)240600(21)FBMHDX00390 FBMHDX00449 (01)00195278096944(11)240900(21)FBMHDX00449 FBMHDX00372 (01)00195278096944(11)240600(21)FBMHDX00372 FBMHDX00377 (01)00195278096944(11)240600(21)FBMHDX00377 FBMHDX00462 (01)00195278096944(11)240900(21)FBMHDX00462 FBMHDX00338 (01)00195278096944(11)240400(21)FBMHDX00338 FBMHDX00423 (01)00195278096944(11)240800(21)FBMHDX00423 FBMHDX00420 (01)00195278096944(11)240800(21)FBMHDX00420 FBMHDX00438 (01)00195278096944(11)240900(21)FBMHDX00438 FBMHDX00432 (01)00195278096944(11)240900(21)FBMHDX00432 FBMHDX00373 (01)00195278096944(11)240600(21)FBMHDX00373 FBMHDX00367 (01)00195278096944(11)240500(21)FBMHDX00367 FBMHDX00446 (01)00195278096944(11)240900(21)FBMHDX00446 FBMHDX00370 (01)00195278096944(11)240600(21)FBMHDX00370 FBMHDX00429 (01)00195278096944(11)240800(21)FBMHDX00429
Where was it sold?
U.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. O.U.S.: Australia, Brazil, Canada, Chile, Costa Rica, India, Italy, Philippines, Poland, Portugal, Sweden, Switzerland, and United Kingdom
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
3 other products · FDA event 95846| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | OEC Elite recalled by GE OEC Medical Systems | GE OEC Medical Systems | Packaging Defects | 44 states | |
| CLASS II | OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System recalled | GE OEC Medical Systems | Packaging Defects | 44 states | |
| CLASS II | OEC 9800 REF Image-Intensified Fluoroscopic X-Ray System recalled | GE OEC Medical Systems | Packaging Defects | 44 states |
More recalls from GE OEC Medical Systems
All 47| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | OEC 9800 REF Image-Intensified Fluoroscopic X-Ray System recalled | GE OEC Medical Systems | Packaging Defects | 44 states |
| Device | CLASS II | OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System recalled | GE OEC Medical Systems | Packaging Defects | 44 states |
| Device | CLASS II | OEC Elite recalled by GE OEC Medical Systems | GE OEC Medical Systems | Packaging Defects | 44 states |
| Device | CLASS II | OEC Elite Systems with Image Intensifier recalled | GE OEC Medical Systems | Other | Nationwide |
| Device | CLASS II | OEC 9800 Systems with Image Intensifier recalled | GE OEC Medical Systems | Other | Nationwide |
Other Surgical Instruments recalls
All 3,883| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Hopkins Telescope 30¿ recalled by Karl Storz Endoscopy | Karl Storz Endoscopy | Packaging Defects | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 24" X 4" 1-Line, Yellow recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Mpr Single Use Tourniquet Cuff 15" 1 Line recalled by ASP Global | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Expressaire Disposable Tourniquet Cuff, 12" X 3.5" 1-Line (CS Plum recalled | ASP Global | Device Malfunction | Nationwide |
| Device | CLASS II | Disposable Tourniquet Cuff, 44" X 4" 2-Line, Green recalled | ASP Global | Device Malfunction | Nationwide |