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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Becton Dickinson & Company: The kits contain surgical gowns which were subject to a recall by the supplier.

Agency Publication Date: May 21, 2020
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Affected Products

Product: BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000025

Lot Numbers: 19ABF426 19BBJ459

Lot Numbers:
Numbers
Product: BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000026A

Lot Numbers: 18JBU370 18OB4147 19BBJ457

Lot Numbers:
Numbers
Product: BARD MYPICC KIT 4F Single-Lumen, Catalog Number CK000276

Lot Numbers: 18JBB605 18KBZ117 19EBE196 19GBG860 19SBH077 19UBA090

Lot Numbers:
Numbers
Product: BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000277

Lot Numbers: 18PB2134 19FBP619

Lot Numbers:
Numbers
Product: BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000278

Lot Numbers: 19FBN919 19GBZ466

Lot Numbers:
Numbers
Product: BARD MYPICC KIT 3F Single-Lumen, Catalog Number CK000417B

Lot Numbers: 18KBN221 18MB9962 18NB2698 19FBK323 19LBB569 19SBH078 19TBD608

Lot Numbers:
Numbers
Product: BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B

Lot Numbers: 18OB4421 18PB2141 19CBK655 19FBJ721 19GBG835 19KBJ097 19TBD597

Lot Numbers:
Numbers
Product: BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000435

Lot Numbers: 18JBU277 18KBY346 18PB0298 19DBQ798 19GBB343 19GBI541

Lot Numbers:
Numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85334
Status: Resolved
Manufacturer: Becton Dickinson & Company
Manufactured In: United States
Units Affected: 8 products (1262 total)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.