PlainRecalls
FDA Devices Moderate Class II Ongoing

CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A

Reported: November 20, 2024 Initiated: October 4, 2024 #Z-0349-2025

Product Description

CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A

Reason for Recall

Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.

Details

Units Affected
36 units
Distribution
US Nationwide distribution in the state of TN.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 36 units.
Why was this product recalled?
Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 20, 2024. Severity: Moderate. Recall number: Z-0349-2025.