Medical Components, Inc dba MedComp Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in attaining long term vascular access for hemodialysis and apheresis in adult patients. Recall
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in attaining long term vascular access for hemodialysis and apheresis in adult patients.
Brand
Medical Components, Inc dba MedComp
Lot Codes / Batch Numbers
TRAY #55216-3, Lot numbers: MBTX960, exp. 10/2016, MBVA850, exp. 10/2016, MBVD080, exp. 01/2017, MBVG680, exp. 01/2017, MBVL020, exp. 01/2017.
Products Sold
TRAY #55216-3; Lot numbers: MBTX960, exp. 10/2016; MBVA850, exp. 10/2016; MBVD080, exp. 01/2017; MBVG680, exp. 01/2017; MBVL020, exp. 01/2017.
Medical Components, Inc dba MedComp is recalling Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in att due to The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath III instead of 28CM.. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath III instead of 28CM.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026