Ansell Healthcare Products LLC MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner s hand or finger to prevent contamination between patient and examiner. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner s hand or finger to prevent contamination between patient and examiner.
Brand
Ansell Healthcare Products LLC
Lot Codes / Batch Numbers
Lot: 2003LG, Batch: 20035314LG
Products Sold
Lot: 2003LG, Batch: 20035314LG
Ansell Healthcare Products LLC is recalling MICROFLEX Diamond Grip Examination Gloves, MF-300 - Product Usage: A patient examination glove is a due to Examination gloves were shipped inadvertently, without to verify barrier integrity.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Examination gloves were shipped inadvertently, without to verify barrier integrity.
Recommended Action
Per FDA guidance
On 08/19/2020, recall notices were emailed to customers who were asked to do the following: If you believe you may have received affected product, please visit: http://www.novasyte.com/ansell/capa-206-2020 to complete the necessary acknowledgement form. Upon completion of the acknowledgement form, Ansell will partner with you to arrange for a return of the product, provide a credit, and offer you the option of a reship. For any assistance regarding the acknowledgement form, please contact Novasyte at 855-863-7288 or ansell-capa-206-2020@novasyte.com Novasyte emailed E-Mail/ Letter for Distributors to Send End-User Customers, Dated 08/18/20, to distributors informing them to send this letter to the end users. End users were asked to return affected products to distributors. On 08/21/2020, the firm followed up with customers via phone.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026