Becton Dickinson Recalls Bard MyPICC Kits Due to Gown Issue
Becton Dickinson is recalling Bard MyPICC Kits because the included surgical gowns were subject to a supplier recall.
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, but the source text does not report any illnesses, injuries, or specific hazards, fitting the criteria for a voluntary precautionary recall or minor issue.
Plain-English summary
Becton Dickinson & Company is recalling Bard MyPICC Kit 5F Triple-Lumen, Catalog Number CK000278. The recall involves 1,262 units of the product.
The reason for the recall is that the kits contain surgical gowns which were subject to a recall by the supplier. The source text does not specify the nature of the defect in the gowns or any associated health risks.
The products were distributed to the following US states: Indiana, Missouri, Ohio, and Texas. The affected lot numbers are 19FBN919 and 19GBZ466. Consumers and healthcare facilities should check their inventory for these specific lot numbers and contact Becton Dickinson for further instructions.
The recalled product
- Product
- BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000278
- Manufacturer
- Becton Dickinson & Company
- Category
- Medical Device — Catheter Kits
- Hazard
- Affected units
- 1,262
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)
- Lot Numbers: 19FBN919 19GBZ466
Distribution
Part of a larger recall action
This product is one of 8 recalled by Becton Dickinson & Company 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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