Lower riskMedical device recall · FDA · Published November 17, 2021
Medshape DYNANAIL MINI Endcap Recall: Risk of Improper Seating During Procedures
Medshape recalls DYNANAIL MINI Endcap +6mm (Ref 2600-05-006) due to potential improper seating during procedures. This sterile medical device, sold with a prescription, may not seat flush with the nail, risking complications.
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.
Take action
Contact the company
📍Recalling firmMedshape, INC.1575 Northside Dr Nw Ste 440 · Atlanta, GA 30318-4211
“Medshape DYNANAIL MINI Endcap Recall: Risk of Improper Seating During Procedures.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61523-medshape-dynanail-mini-endcap-recall-risk-of-improper-seating-during. Based on FDA recall #Z-0453-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0453-2022%22&limit=1).
The FDA announced on 2021-11-17 that Medshape, INC. is recalling DYNANAIL MINI Endcap +6mm units due to a nonconformance risk. The hazard involves the endcap being manufactured to a longer length than specified.
How to tell if you have it
Brand: Medshape
Product: DYNANAIL MINI, Endcap +6mm
Model No.: 2600-05-006
Lot No.: 04882
UDI: M97026000500060
The hazard
The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications. This introduces the risk of the +6 mm endcap not seating flush with the nail while inserting during a procedure.
Context
GovInfoNow's records show Medshape, INC. has 1 other recall on record since 2025-06-02. On 2025-06-02, Medshape issued a Universal Joints Recall citing the risk of frame instability during surgery. Other recent recalls of similar products include Wilson-Cook Instinct Plus Endoscopic Clipping Device Recall (2026-03-03), Merit Medical Custom Procedure Kit Recall (2025-12-04), and Medline Forceps Recall (2025-11-13).
How to tell if you have this one
Check for the model number 2600-05-006 and lot number 04882 on the device. This sterile device is sold with a prescription and is intended for medical procedures.
Brand
Medshape
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Details
Verify the model number (2600-05-006) and lot number (04882) on the device to confirm it is recalled.
Where it went and when
Where it was distributed
Distributed in 9 states.
Listed by the agency
Not listed
FDA distribution: “Domestic: CA, FL, GA, IL, IN, MA, MD, TX, and WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0453-2022 (November 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0453-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.