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Open, Classified

Regard CV PK, Item Numbers a) 880289014, b) 880289015; cardiovascular convenience kit

FDA Recall Z-0315-2024 · Posted 2023-11-16

Recalling FirmROi CPS LLC
Recall StatusOpen, Classified
Product CodeOEZ
Date Initiated2023-09-21
Product Quantity134 units

Reason for Recall

Specific Regard kits contain the Gentige Chest Drain Products being recalled by Gentige. The Instructions for Use (IFU) for the chest drains do not provide sufficient precaution instruction for proper set up of catheter(s) and patient tube connections with single collection chamber chest drains.

Firm Action

ROi CPS, LLC issued an URGENT MEDICAL DEVICE CORRECTION NOTICE to its sole consignee on 09/29/2023 via email. The email attached the notice and the notice received from Getinge. The notice explained the issue, the potential risks, and requested the distributor notify their customer. End user was directed to post the Getinge notice in area where the affect kits were used. An updated notice was sent on 10/13/2023 via email with the corrected item numbers with the same instructions.

Root Cause

Other

Distribution Pattern

MO

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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