DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model No. 2600-05-006; Lot No. 04882; UDI: M97026000500060
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Medshape, INC.
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Product Codes/Lot Numbers:
Model No. 2600-05-006; Lot No. 04882; UDI: M97026000500060
Distribution:
Distributed in: CA, FL, GA, IL, IN, MA, MD, TX, WA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0453-2022
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