Baxter Healthcare Corporation: Medical Device Recall in 2022 - (Recall #: Z-0176-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

C-Flex Polar Head Positnr-Device Only, SSP-NEUROSURGICAL HEADREST, REF A-70701, #103001,

Product Classification:

Class II

Date Initiated: September 20, 2022

Date Posted: November 9, 2022

Recall Number: Z-0176-2023

Event ID: 90848

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 2 units

Code Information:

UDI/DI 00615521002701, Lot Numbers: 122190000182, 122190001101

Distribution Pattern:

MI, BA, WI, WA, TX, and Germany, Japan, South Korea, Sweden, South Africa

Voluntary or Mandated:

Voluntary: Firm initiated