Issued
Manufacturer
Literature
Notice
02/06/2026
HUB Pharmaceuticals
URGENT DRUG RECALL – Specific lots of BioGlo Ophthalmic Test Strip. This notice has been issued because it was not manufactured in conformance with current good manufacturing practices. Affected products first shipped June 1, 2021. This Urgent Drug Recall is being done with the knowledge of the U.S. Food and Drug Administration. VeriCor LLC has taken appropriate action per this notice. Affected customers were identified and notified with further instructions.
01/26/26
Cardinal Health
URGENT MEDICAL DEVICE PRODUCT ADVISORY NOTIFICATION – Instructions for use (IFUs) on all lots of various Chest Drainage Units. This notice has been issued to communicate to customers that the instructions for use on the listed Cardinal Health Chest Drainage Units and accessories have been updated to clarify the intended target patient population as adults, 18 years and older. Affected products first shipped January 1, 2020. VeriCor, LLC has taken appropriate action per the notice. Affected customers were identified and notified with further instructions.
10/20/2025
Cardinal Health
URGENT MEDICAL DEVICE CORRECTION NOTIFICATION – All lots of their Salen Sump Products. This notice has been issued to provide additional guidance on how to properly us the Anti-Reflux Valve (ARV). Affected products first shipped August 1, 2020. Affected customers were identified and notified with further instructions.
09/22/2025
DermaRite
URGENT PRODUCT RECALL – All lots of various products. This notice has been issued due to certain individual lots of products having microbial contamination that exceeds the acceptable limits set by the FDA. The FDA has advised that the presence of elevated microbial levels may pose a risk of localized skin irritation or infection due to elevated bacterial levels. Out of an abundance of caution, DermaRite is now expanding the recall to include all lots of the affected products and additional products. Affected products first shipped August 1, 2023. VeriCor, LLC has taken appropriate action per the notice. Affected customers were identified and notified with further instructions.
12/11/23
Cardinal Health
URGENT PRODUCT RECALL – Specific lots of their Kits and Trays containing Nurse Assist Products. This notice has been issued because Nurse Assist, LLC products cannot be verified as having the required sterility assurance level of (SAL) of 10-6. 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. Affected product first shipped November 1, 2021. VeriCor, LLC has taken appropriate action per the notice. Affected customers were identified and notified with further instructions.
11/9/23
Nurse Assist, LLC
URGENT FIELD SAFETY NOTICE – Specific lots of Sterile 0.9% Normal Saline, USP. This notice was issued because the product cannot be verified as having the required sterility assurance level of (SAL) 10-6. The affected product first shipped on November 1, 2021. VeriCor, LLC has taken appropriate action per the notice. Affected customers were identified and notified with further instructions.
6/19/23
Teleflex LLC
RECALL – Specific lots of Teleflex Endotracheal Tubes (ET tube). This notice has been issued due to reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. There is the possibility of oxygen desaturation and in the event any immediate and long-term health consequences are dependent on the degree and duration of desaturation, which may include serious injury or death. Affected product first shipped June 14, 2018. VeriCor, LLC has taken appropriate action per the notice. Affected customers were identified and notified with further instructions.
4/26/23
Akorn
RECALL – All Akorn products and lots within expiry. This notice has been issued due to the discontinuation of Quality activities as a result of Akorn filing Chapter 7 bankruptcy on February 23, 2023. VeriCor, LLC has taken appropriate action per the notice. Affected customers were identified and notified with further instructions.
3/4/20
VeriCor
URGENT PRODUCT NOTIFICATION-EVD Sold Post 2018: The purpose of this letter is to advise you about a product sold after August 1, 2018. According to records, you received one or more of the following EVD products.
3/4/20
VeriCor
URGENT PRODUCT NOTIFICATION-EVD Sold 2014-2018: The purpose of this letter is to advise you about a product sold between August 1, 2014, and August 1, 2018. According to records, you received one or more of the following EVD products.
10/2/18
B. Braun Medical
RECALL – Rate Flow Regulator: This is to inform you that B. Braun Medical Inc. (BBMI) is issuing a voluntary medical device recall of Rate Flow® Regulator Administration sets due to reported deficiencies in the manufacturer’s quality systems at its manufacturing facility. Rate Flow Regulator Administration sets are manufactured by Leventon S.A.U. and purchased as a finished product by BBMI.
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