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.
Medshape is recalling its DYNANAIL MINI Endcap +6mm (Ref 2600-05-006) because the endcap may not seat flush with the nail during procedures. This could lead to complications if the device is used incorrectly.
The endcap is manufactured to a longer length than specified, which can cause it to not seat flush with the nail during procedures. This may lead to complications such as improper device function or injury.
Healthcare professionals who use this sterile medical device for procedures are likely affected. Patients receiving this device under a prescription are at risk if the endcap does not seat properly.
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.
Verify the model number (2600-05-006) and lot number (04882) on the device to confirm it is recalled.
The recall indicates a potential risk of improper seating during procedures, so it is not recommended for use until the recall is addressed.
Look for the model number 2600-05-006 and lot number 04882 on the device, which is sold with a prescription.
Check the device details to confirm it is recalled; if it is, contact Medshape for further instructions.
We’ve drafted a message you can send Medshape to request your refund or repair — edit it as you like.
Subject: Recall Z-0453-2022 — Medshape Medshape Hello, I own a Medshape that is covered by recall Z-0453-2022 from Medshape. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
