Vygon Recalls Heparin Lock Flush Syringes and Kits
Vygon Corporation is voluntarily recalling Heparin Lock Flush Syringes and kits containing them due to a related recall of VY Flush Heparin Lock Flush Syringes.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and is described as a voluntary precautionary measure triggered by a related recall, with no reported illnesses or injuries in the source text.
Plain-English summary
Vygon Corporation has initiated a voluntary recall of Vygon branded Heparin Lock Flush Syringes and kits containing these syringes. This action follows a separate voluntary recall issued by the manufacturer for multiple lots of VY Flush Heparin Lock Flush Syringes.
The recalled products include the Churchill Medical Systems, Inc. PORT-A-CATH Tray Kit, which contains prefilled syringes used to maintain the patency of indwelling catheter lumens. The specific product code is AMS-9889CP-7, lot 10I86.
Distribution was nationwide, including Arizona, California, Delaware, Florida, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, West Virginia, and Wisconsin. The source text does not specify the number of units recalled or report any illnesses or injuries associated with the product.
The recalled product
- Product
- Churchill Medical Systems, Inc. PORT-A-CATH Tray Kit Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
- Manufacturer
- Vygon Corporation
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Product Code AMS-9889CP-7 -- lot 10I86.
Distribution
Part of a larger recall action
This product is one of 12 recalled by Vygon Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 12 products in this recall →Related recalls
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