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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79342

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

Open FDA event record

Event summary

Timeline bucket
November 14, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Arrow International Inc

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

9 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 9

Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits venous access and catheter introduction to the central circulation.

Z-1158-2018
Recall number
Z-1158-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

ASK-09903-ECL 23F16H0387 23F16H0595

Distribution pattern

Nationwide Distribution

device · product 2 of 9

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features and Maximal Barrier Precautions. Permits venous access and catheter introduction to the central circulation.

Z-1159-2018
Recall number
Z-1159-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

ASK-15703-PWBH 13F16K0166

Distribution pattern

Nationwide Distribution

device · product 3 of 9

Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters. Permits venous access and catheter introduction to the central circulation.

Z-1160-2018
Recall number
Z-1160-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

ASK-29803-SJH 13F16K0136

Distribution pattern

Nationwide Distribution

device · product 4 of 9

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features, and Maximal Barrier Precautions. Permits venous access to central circulation.

Z-1161-2018
Recall number
Z-1161-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

ASK-42703-PSCH 23F16H0492

Distribution pattern

Nationwide Distribution

device · product 5 of 9

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and Sharps Safety Features. Permits venous access to central circulation.

Z-1162-2018
Recall number
Z-1162-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

ASK-45703-PNCB 23F16H0802

Distribution pattern

Nationwide Distribution

device · product 6 of 9

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter, Sharps Safety Features and Maximal Barrier Precautions. Permits venous access to central circulation.

Z-1163-2018
Recall number
Z-1163-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

ASK-45703-PUR1 23F16H0385

Distribution pattern

Nationwide Distribution

device · product 7 of 9

Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and Sharps Safety Features. Permits venous access to central circulation.

Z-1164-2018
Recall number
Z-1164-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

ASK-45802-PHMW 13F16K0236

Distribution pattern

Nationwide Distribution

device · product 8 of 9

Pressure Injectable Multi- Lumen CVC Kit

Z-1165-2018
Recall number
Z-1165-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

CDC-15703-P1A 13F16J0336

Distribution pattern

Nationwide Distribution

device · product 9 of 9

ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to permit venous access to the central circulation.

Z-1166-2018
Recall number
Z-1166-2018
Initiated
November 14, 2017
Classification
Class II
Status
Terminated
Recalling firm
Arrow International Inc
Quantity
18,124 total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.

Code information

CDC-42703-P1A CDC-45703-P1A 13F16H0215 13F16H0216 13F16J0157 13F16J0053 13F16J0182 13F16J0186 13F16K0119 13F16K0266

Distribution pattern

Nationwide Distribution

Field note

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