FDAAugust 22, 2024device

System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Xper FD20/15 722039 Allura Xper FD20/20 OR Table 722038 Allura Xper FD20/20 722035 Allura Xper FD20 OR Table 722029 Allura Xper FD20/10 722028 Allura Xper FD20 722027 Allura Xper FD10/10 722026 Allura Xper FD10 722025 Allura Xper FD20...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or bolts) which May Result in Parts Falling and/or Part of the Cable Hose Dropping, and result in injury.

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

008848380591220088483805911500884838054226008848380542400088483805421900884838054202008848380541960088483805418900884838059061008848380590540088483805903000884838055513

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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