🔍 RecallPedia

SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210

Class I - Dangerous
🏥 Medical Devices Recalled: February 21, 2023 Limacorporate S.p.A Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    UDI-DI/Lot/Expiration: 08033390121798/2206565/2027-04-30
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:
Limacorporate S.p.A
Reason for Recall:
Shoulder glenoid fossa prosthesis was manufactured without tantalum markers so in the absence of the markers, on already implanted devices, a correct radiographic assessment of the hybrid glenoid position can be performed by the evaluation of the joint space, central TT peg position and cement mantel observation.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210

Product Codes/Lot Numbers:

UDI-DI/Lot/Expiration: 08033390121798/2206565/2027-04-30

Distribution:

Distributed in: US, MO

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1317-2023

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