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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85334

8 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 26, 2020
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Becton Dickinson & Company

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

8 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 8

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

Z-2075-2020
Recall number
Z-2075-2020
Initiated
February 26, 2020
Classification
Class II
Status
Terminated
Quantity
1262 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The kits contain surgical gowns which were subject to a recall by the supplier.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Lot Numbers: 19ABF426 19BBJ459

Distribution pattern

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

device · product 2 of 8

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

Z-2076-2020
Recall number
Z-2076-2020
Initiated
February 26, 2020
Classification
Class II
Status
Terminated
Quantity
1262 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The kits contain surgical gowns which were subject to a recall by the supplier.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Lot Numbers: 18JBU370 18OB4147 19BBJ457

Distribution pattern

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

device · product 3 of 8

BARD MYPICC KIT 4F Single-Lumen, Catalog Number CK000276

Z-2077-2020
Recall number
Z-2077-2020
Initiated
February 26, 2020
Classification
Class II
Status
Terminated
Quantity
1262 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The kits contain surgical gowns which were subject to a recall by the supplier.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

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

device · product 4 of 8

BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000277

Z-2078-2020
Recall number
Z-2078-2020
Initiated
February 26, 2020
Classification
Class II
Status
Terminated
Quantity
1262 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The kits contain surgical gowns which were subject to a recall by the supplier.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Lot Numbers: 18PB2134 19FBP619

Distribution pattern

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

device · product 5 of 8

BARD MYPICC KIT 5F Triple-Lumen, Catalog Number CK000278

Z-2079-2020
Recall number
Z-2079-2020
Initiated
February 26, 2020
Classification
Class II
Status
Terminated
Quantity
1262 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The kits contain surgical gowns which were subject to a recall by the supplier.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Lot Numbers: 19FBN919 19GBZ466

Distribution pattern

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

device · product 6 of 8

BARD MYPICC KIT 3F Single-Lumen, Catalog Number CK000417B

Z-2080-2020
Recall number
Z-2080-2020
Initiated
February 26, 2020
Classification
Class II
Status
Terminated
Quantity
1262 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The kits contain surgical gowns which were subject to a recall by the supplier.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

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

device · product 7 of 8

BARD MYPICC KIT 4F Dual-Lumen, Catalog Number CK000418B

Z-2081-2020
Recall number
Z-2081-2020
Initiated
February 26, 2020
Classification
Class II
Status
Terminated
Quantity
1262 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The kits contain surgical gowns which were subject to a recall by the supplier.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

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

device · product 8 of 8

BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000435

Z-2082-2020
Recall number
Z-2082-2020
Initiated
February 26, 2020
Classification
Class II
Status
Terminated
Quantity
1262 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The kits contain surgical gowns which were subject to a recall by the supplier.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

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