CLASS II Device recall · Reported 27 May 2020 · FDA Enforcement Report

Bard Mypicc Kit 5F Triple-Lumen recalled by Becton Dickinson &

Becton Dickinson & is recalling Bard Mypicc Kit 5F Triple-Lumen, distributed in Indiana, Missouri, Ohio, Texas. The recall was initiated on 26 Feb 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Numbers: 18JBU370 18OB4147 19BBJ457
Quantity recalled1262 total

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-2076-2020
FDA event ID
85334
Recalling firm
Becton Dickinson &, Franklin Lakes, NJ
Classification
Class II
Status
Terminated
Recall initiated
26 Feb 2020
FDA classified
21 May 2020
Reported
27 May 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

26 Feb 2020Recall initiated by company
21 May 2020Classified by FDA+85 days
27 May 2020Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The kits contain surgical gowns which were subject to a recall by the supplier.

Product as listed by the FDA

BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000026A

Where it was distributed

The products were distributed to the following US states: IN, MO, OH, and TX.

IndianaMissouriOhioTexas

Questions about this recall

Is Bard Mypicc Kit 5F Triple-Lumen recalled?

Yes. Becton Dickinson & recalled Bard Mypicc Kit 5F Triple-Lumen on 26 Feb 2020. The recall is Class II and its status is Terminated. Recall number Z-2076-2020.

Why was it recalled?

The kits contain surgical gowns which were subject to a recall by the supplier.

Which lots are affected?

Lot Numbers: 18JBU370 18OB4147 19BBJ457

Where was it sold?

The products were distributed to the following US states: IN, MO, OH, and TX.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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