PlainRecalls
FDA Devices Moderate Class II Ongoing

Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-13 (SPI Elast. Sleeve 8-13), Catalog Number 18061407S

Reported: August 11, 2021 Initiated: May 27, 2021 #Z-2170-2021

Product Description

Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-13 (SPI Elast. Sleeve 8-13), Catalog Number 18061407S

Reason for Recall

The devices have a different inner diameter than the diameter specified on the outer box label.

Details

Recalling Firm
Stryker GmbH
Units Affected
52
Distribution
US Nationwide Distribution
Location
Selzach

Frequently Asked Questions

What product was recalled?
Nail Insertion Sleeve, elastic T2 Tibia SPI ¿8-13 (SPI Elast. Sleeve 8-13), Catalog Number 18061407S. Recalled by Stryker GmbH. Units affected: 52.
Why was this product recalled?
The devices have a different inner diameter than the diameter specified on the outer box label.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 11, 2021. Severity: Moderate. Recall number: Z-2170-2021.