Medshape, INC. DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Brand
Medshape, INC.
Lot Codes / Batch Numbers
Model No. 2600-05-006, Lot No. 04882, UDI: M97026000500060
Products Sold
Model No. 2600-05-006; Lot No. 04882; UDI: M97026000500060
Medshape, INC. is recalling DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile due to The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications,. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not seating flush with the nail while inserting during a procedure.
Recommended Action
Per FDA guidance
The firm indicated that they will send recall notification to sales representatives via email or certified mail. Customers will be instructed to remove all +6 mm endcaps from stock and to return to the recalling firm with a return label that will be provided at a later date. Customers with questions are to contact the recalling firm at (678)235-3314.
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 noticeDistribution
As reported by FDA
CA, FL, GA, IL, IN, MD, MA, TX, WA
Page updated: Jan 10, 2026