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. The source text does not report any illnesses, injuries, or deaths, and the hazard is limited to a component (surgical gowns) subject to a supplier recall without specified severe consequences, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Becton Dickinson & Company is recalling the Bard MyPICC Kit 4F Single-Lumen, Catalog Number CK000276. 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 exact nature of the defect in the gowns or any reported injuries.
The products were distributed to the following US states: Indiana (IN), Missouri (MO), Ohio (OH), and Texas (TX). Affected lot numbers include 18JBB605, 18KBZ117, 19EBE196, 19GBG860, 19SBH077, and 19UBA090. Healthcare facilities and consumers should check their inventory for these specific lot numbers and contact Becton Dickinson for instructions on how to return the product.
The recalled product
- Product
- BARD MYPICC KIT 4F Single-Lumen, Catalog Number CK000276
- Manufacturer
- Becton Dickinson & Company
- Category
- Medical Device — PICC Kits
- 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: 18JBB605 18KBZ117 19EBE196 19GBG860 19SBH077 19UBA090
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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