Recall StatusTerminated
Date Initiated2021-06-09
Date Terminated2023-11-01
Product Quantity2,911,064 units
Reason for Recall
A caution statement is being added to remind the
user to activate away from face and infant as reports of pack rupture or leaking during activation may
resulting in the contents splashing into the user s eyes or onto the infant. Potential harms associated with contact of the liquid inside the pouch are rash, burn and inflammation.
Firm Action
Cardinal Health issued a "MEDICAL DEVICE PRODUCT ADVISORY" letter and Acknowledgement Form dated 6/9/2021 via overnight mail to the direct consignees on June 09, 2021.
Letters states reason for issuance, health risk associated and action to take:
The caution statement on the labeling will be updated to remind the user to activate away from face and infant. The full caution statement will now state:
Caution: Activate away from face and infant. If pack ruptures or contents leak, flush contact area with water. Discard pack. If redness or irritation persists, consult a physician. What actions are needed from the Customer?
Please review this enhanced caution statement with your staff to ensure product activation is performed away from the face and infant.
For questions related to this notification and/or acknowledgement form that are not adequately addressed in this letter, please contact the market action team at:
[email protected] or call 800-292-9332.
In the event you have experienced quality problems or adverse events related to the products listed above, please contact
[email protected]
Root Cause
Package design/selection
Distribution Pattern
US Nationwide Distribution to states of: AK, AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, IA ,ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WY.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.