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

Bard Mypicc Kit 4F Dual-Lumen recalled by Becton Dickinson &

Becton Dickinson & is recalling Bard Mypicc Kit 4F Dual-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: 18OB4421 18PB2141 19CBK655 19FBJ721 19GBG835 19KBJ097 19TBD597

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-2081-2020
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
Device type: Other Medical Devices

Timeline

26 Feb 2020	Recall initiated by company
21 May 2020	Classified by FDA	+85 days
27 May 2020	Published 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 4F Dual-Lumen, Catalog Number CK000418B

Where it was distributed

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

Indiana Missouri Ohio Texas

Questions about this recall

Is Bard Mypicc Kit 4F Dual-Lumen recalled?

Yes. Becton Dickinson & recalled Bard Mypicc Kit 4F Dual-Lumen on 26 Feb 2020. The recall is Class II and its status is Terminated. Recall number Z-2081-2020.

Why was it recalled?

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

Which lots are affected?

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

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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