Becton Dickinson Recalls Bard MyPICC Kits Due to Gown Recall
Becton Dickinson is recalling 1,262 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, and the source text does not report any illnesses, injuries, or specific hazards associated with the surgical gowns, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Becton Dickinson & Company is recalling 1,262 units of the Bard MyPICC Kit 3F Single-Lumen, Catalog Number CK000417B. The recall is being conducted because the kits contain surgical gowns that were subject to a separate recall by the supplier.
The affected products were distributed to the following US states: Indiana, Missouri, Ohio, and Texas. The specific lot numbers involved are 18KBN221, 18MB9962, 18NB2698, 19FBK323, 19LBB569, 19SBH078, and 19TBD608.
Healthcare facilities and consumers should check their inventory for these specific lot numbers and stop using the affected kits. For more information, contact Becton Dickinson & Company or refer to the FDA recall notice Z-2080-2020.
The recalled product
- Product
- BARD MYPICC KIT 3F Single-Lumen, Catalog Number CK000417B
- Manufacturer
- Becton Dickinson & Company
- Category
- Medical Device — Surgical Kits
- Hazard
- Affected units
- 1,262
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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