Becton Dickinson Recalls Bard MyPICC Kits Due to Surgical Gown Issue
Becton Dickinson is recalling Bard MyPICC Kits because the included surgical gowns were subject to a supplier recall.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Becton Dickinson & Company is recalling the Bard MyPICC Kit 4F Dual-Lumen, Catalog Number CK000418B. 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 surgical gowns or any associated health risks.
The products were distributed to the following US states: Indiana, Missouri, Ohio, and Texas. Affected lot numbers are 18OB4421, 18PB2141, 19CBK655, 19FBJ721, 19GBG835, 19KBJ097, and 19TBD597. Healthcare facilities should check their inventory for these specific lot numbers and stop using the affected kits.
The recalled product
- Product
- BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B
- Manufacturer
- Becton Dickinson & Company
- 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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