Vygon MFG, Inc., dba/ Churchill Medical Systems 4Fr x 20cm Single Lumen CT Midline Basic recall — FDA Z-0585-2020
Potential that 3Fr size catheter placed in the catheter tray instead of 4Fr for the 4Fr x 20cm Single Lumen CT Midline Basic Tray.
Overview of recall records associated with Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Potential that 3Fr size catheter placed in the catheter tray instead of 4Fr for the 4Fr x 20cm Single Lumen CT Midline Basic Tray.
The Iodine Prep Pads within the Vygon IV Start Convenience Kits, had stability samples that were not meeting iodine assay level requirements to support the 36 month expiration date. All…
This page summarizes recall records in which the official source identifies Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.