Recall StatusTerminated
Date Initiated2018-05-14
Date Terminated2021-08-05
Product Quantity1360 units
Reason for Recall
In vitro diagnostic devices, used greater than 6 months after date of manufacture, may have increased concentration times of greater than the specification of 3 hours and up to 24 hours, which may lead to delays in carrying out the subsequent analysis tests.
Firm Action
On May 14, 2018, the firm sent an "Urgent Field Safety Notice" to customers via email and following up with a hard-copy letter on June 6, 2018 via United States Postal Services. The letter described the product, problem and actions to be taken. The corrective action being taken by the firm is to reduce the shelf life of the device from 12 months to 6 months.
The customers are being instructed to immediately examine their inventory to determine if they have any remaining impacted product and forward a copy of this letter to the personnel in your organization that utilize this product and/or need to be made aware of this issue.
In addition, if the customer has further distributed this product, please identify its customers and notify them at once of this issue. The notification to their customers should include a copy of this notification and attachment 2
Customers are instructed to please stop use of these lots if older than 6 months and destroy any remaining inventory older than 6 months, and to complete and return the receipt confirmation form to
[email protected].
If you would like more information regarding this notification, please contact us at
[email protected] or go to our website to find the phone number of your local office at www.emdmillipore.com/offices.
Root Cause
Process control
Distribution Pattern
Worldwide Distribution: US (nationwide) to states of: AZ, CA, CT, DC, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NJ, NY, OH, OK,OR, PA, RI, TN, TX, VA, VT, WA and WI; and countries of: Canada and Australia.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.