Z-2171-2021 Class II Ongoing
FDA device recall Z-2171-2021 was initiated by Stryker GmbH on May 27, 2021 and is designated Class II. Reason for recall: The devices have a different inner diameter than the diameter specified on the outer box label. The recall status is ongoing. Affected quantity: 242.
Recall Details
- Product Type
- Devices
- Report Date
- August 11, 2021
- Initiation Date
- May 27, 2021
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 242
Product Description
Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-11 (SPI Elast. Sleeve 8-11), Catalog Number 18061406S
Reason for Recall
The devices have a different inner diameter than the diameter specified on the outer box label.
Distribution Pattern
US Nationwide Distribution
Code Information
GTIN 04546540715357, Lot Number K03CC4F