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Baxter Healthcare Corporation recalls C-Flex Polar Head Positnr-Device Only, SSP-NEUROSURGICAL HEADREST, REF A-70701, #103001,
Recalled November 9, 2022 · FDA recall Z-0176-2023 · Baxter Healthcare
Hazard
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity. · FDA Class II
Units
2 units
Sold at
MI, BA, WI, WA, TX, and Germany, Japan, South Korea, Sweden, South Africa
Description
the adhesive, applied to screws and bolts as an additional holding force, may not cure correctly, and as a result, could result in a loss of holding and reduced mechanical integrity.
Product
C-Flex Polar Head Positnr-Device Only, SSP-NEUROSURGICAL HEADREST, REF A-70701, #103001,
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →