Cardinal Health Issues Medical Device Recall for Nurse Assist Products Contained Within Kits/Trays


Medical Recalls

daptomycin
Rae Prenatal Capsules
nationwide pharmaceutical ferrous sulfate

In direct response to the Nurse Assist, LLC voluntary product recall (which included products supplied to Cardinal Health used in Covidien and Cardinal Health™ brand kits and trays), Cardinal Health issued a medical device recall on December 5, 2023, for its Covidien and Cardinal Health™ brand urology and operating room-specific kits and trays that contain 0.9% sodium chloride irrigation USP and sterile water for irrigation USP supplied by Nurse Assist. Under the Nurse Assist voluntary recall, this product is being recalled due to the potential for a lack of sterility assurance which could result in non-sterile product.

In populations most at risk, such as patients who are immunocompromised, there is a possibility that the use of the affected product could potentially result in severe or life-threatening adverse events. There have been no reports of patient harm. Our top priority is the safety of patients.

After reviewing the impact of the Nurse Assist recall, Cardinal Health has identified the below affected Covidien and Cardinal Health™ brand codes and lot numbers.

Customers who received the listed lots were given instructions to:

  • QUARANTINE affected kits/trays.
  • ALERT clinicians of the recalled component(s).
  • AFFIX a WARNING LABEL to the front of each kit/tray so that it is clearly visible to clinicians, instructing them to remove and discard the recalled component(s).
  • NOTIFY other departments, facilities or customers within the customer’s hospital system, if they have transferred the affected kits/trays, and provide a copy of the notice and recall acknowledgement form to them.
  • RETURN their enclosed Acknowledgment Form confirming receipt of this action and the completion of over labeled product via fax to 614.652.9648.

Source: FDA

You Are Leaving Us

This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.

Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.

Consumer Contact: -

For additional questions related to this recall, please reach out to: fieldcorrectiveaction@cardinalhealth.com or call 800-292-9332.

You Are Leaving Us

This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.

Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.

You Are Leaving Us

This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.

Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.

You Are Leaving Us

This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.

Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.

You Are Leaving Us

This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.

Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.


Related Posts

volara system
Baxter Issues Urgent Medical Device Recall for Volar System Single-Patient Use Circuit
Baxter Issues Urgent Medical Device Recall for Volar System Single-Patient Use Circuit
umary acido hialuronica
SoloVital Recalls Umary Acido Hialuronica, Suplemento Alimenticio 850 mg Capsules
SoloVital Recalls Umary Acido Hialuronica, Suplemento Alimenticio 850 mg Capsules
hard steel logo
Supercore Products Group, Inc. Recalls Hard Steel Capsules and Gold Hard Steel Plus Liquid
Supercore Products Group, Inc. Recalls Hard Steel Capsules and Gold Hard Steel Plus Liquid
life 2000 ventilator
Baxter Recalls Life2000 Ventilator due to Charger Issues
Baxter Recalls Life2000 Ventilator due to Charger Issues

Latest Posts

bissell steam shot handheld steam cleaner
BISSELL Recalls More Than 3 Million Steam Shot Handheld Steam Cleaners Due to Burn Hazard
manhattan toy brilliant bee rattle
Sassy Baby Recalls Manhattan Toy Brilliant Bee Rattles Due to Choking Hazard
cfmoto zforce 950 ho sport side by side rov
CFMOTO Recalls ZFORCE 950 Recreational Off-Highway Vehicles
clonazepam orally disintegrating tablets
Endo USA, Inc. Recalls Lot 550147301 of Clonazepam Orally Disintegrating Tablets
one of the recalled hotdog products
AW Farms Recalls Ready-To-Eat Hot Dog Products

Leave a Reply

Your email address will not be published. Required fields are marked *

You Are Leaving Us

This link is being provided as a convenience and for informational purposes only it is not an endorsement or an approval of any of the products, services or opinions of the corporation or organization or individual.

Recallinsider.com bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links.