AngioDynamics Recalls PICC Kits Containing Recalled BD Syringes
AngioDynamics is recalling certain PICC Kits because they contain BD PosiFlush SF Saline Flush Syringes that were previously recalled by BD Medical.
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: This is a precautionary recall of a medical device kit due to the inclusion of a component (BD syringes) that was previously recalled. The source text does not report any injuries, illnesses, or specific hazards associated with the AngioDynamics kits themselves, fitting the criteria for a voluntary precautionary recall.
Plain-English summary
AngioDynamics, Inc. is recalling certain PICC Kits. The recall is necessary because these kits contain BD PosiFlush SF Saline Flush Syringes that were subject to a separate recall by BD Medical on April 16, 2020.
The source text does not specify the exact reason for the original BD Medical recall, the specific lot numbers of the AngioDynamics kits, or the number of units affected. It does not report any illnesses or injuries associated with this specific recall notice.
Healthcare providers and consumers should check their inventory for these specific PICC Kits. If the kits contain the affected BD syringes, they should stop using them and contact AngioDynamics for instructions on return or replacement.
The recalled product
- Product
- BioFlo Midline Catheter and BioFlo Maximal Barrier Kits - Product Usage: These introducers are used for the percutaneous introduction of diagnostic or therapeutic devices, such as catheters or pacing leads in the vasculature. Item Numbers H965460151 H965460161 H965460161-NP
- Manufacturer
- Angiodynamics, Inc.
- Category
- Medical Device — Catheter Kits
- Hazard
- Affected units
- 119,723
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 (2)
- therefore
- removed from recall notification.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 recalled by Angiodynamics, Inc. 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.
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