Reported Jul 17, 2024 · Ongoing
VidiaPort carrying arm, mount for auxiliary products, model numbers: a) 4028110 (Ceiling Single Surgical Light); b)…
Baxter Healthcare Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- VidiaPort carrying arm, mount for auxiliary products
- model numbers
a) 4028110 (Ceiling Single Surgical Light)b) 4028210 (Ceiling Duo Surgical Lights)c) 4028310 (Ceiling Trio Surgical Lights)
- Lot codes and dates
- a) UDI/DI 00887761968523
- Serial Numbers
108664155108664156108669683108669684108673461108696617108726885108731089108746956108754496108754497108821898108835099108907603108909646108917888108919439108919440108919441108961413108961414108970453108970454b) UDI/DI 00887761968462
- Serial Numbers
203 of 203 codes
108645027108645028108645031108648403108652874108664909108664911108665618108669680108669681108669682108671489108671494108671495108671496108671497108671498108671499108671500108674055108674056108674057108674058108676619108676620108676621108677352108677353108678974108678975108680874108680875108680877108683306108692868108696905108698871108712900108713005108724511108724512108726889108726890108726969108726970108729819108729820108729821108729822108740036108740037108741241108741242108741243108741244108741245108741246108746957108746958108750621
- Serial Numbers
108592036108611920108619324108648397108648399108653145108664152108665620108671478108671479108671488108757703108778413108784863108832046108832147108835101108892991108896993108896994108917886108917889108933948108933952108933958108941393108941394108941395108941397108949663108949664108949665108949666108949667108949668108966760108966761108966762108966763108966764108966765108966766108966767108973046108973047108973048108973049108978929108982386108982387
- Amount recalled
- 275 units
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Why it was recalled
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted as they are equipped with iLED 7 light-heads
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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