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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82350

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

Open FDA event record

Event summary

Timeline bucket
March 05, 2019
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

2 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 2

Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07

Z-1120-2019
Recall number
Z-1120-2019
Initiated
March 05, 2019
Classification
Class II
Status
Terminated
Quantity
21220 total cases of 20

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.

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 firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.

Code information

18105594 18105595 18105596 18105597

Distribution pattern

Distributed to accounts in AL, CA, DC, FL, LA, MD, NE, TN, VA, and WA.

device · product 2 of 2

Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07

Z-1121-2019
Recall number
Z-1121-2019
Initiated
March 05, 2019
Classification
Class II
Status
Terminated
Quantity
21220 total cases of 20

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.

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 firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.

Code information

18105828 18105830 18105857 18105858

Distribution pattern

Distributed to accounts in AL, CA, DC, FL, LA, MD, NE, TN, VA, and WA.