Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet, R
Summary
The FDA issued a Class I for Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-l by ARROW INTERNATIONAL Inc.. Reason: This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits..
Details
Source
Device Recall
External ID
Z-0001-2024
Action Date
2023-10-11
Status
Ongoing
Category
device
Product Description
Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet, REF CDC-45552-VPS2; Catheter: Percutaneous Implanted Long-Term Intravascular Catheter Stylet: Diagnostic Intravascular Catheter
Lot/Code Info: Batch/Lot number 33F23B0781
Quantity Affected: 1173 units
Reason for Recall
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Distribution
US
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-10
Company
Morrisville, NC
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 142 device recalls issued in the same week, part of 403 device-related FDA actions this month.
ARROW INTERNATIONAL Inc. has 55 FDA actions in our database, including 55 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ARROW INTERNATIONAL Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ARROW INTERNATIONAL Inc. have FDA actions?
ARROW INTERNATIONAL Inc. has 55 FDA actions in our database, including 55 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0001-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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