PlainRecalls
FDA Devices Moderate Class II Ongoing

FESS-MB PACK-LF Convenience kit, SKU DYNJ0888159I. Convenience kits used for various procedures..

Reported: January 1, 2025 Initiated: November 6, 2024 #Z-0718-2025

Product Description

FESS-MB PACK-LF Convenience kit, SKU DYNJ0888159I. Convenience kits used for various procedures..

Reason for Recall

Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods

Details

Units Affected
36 kits
Distribution
US Nationwide. Canada.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
FESS-MB PACK-LF Convenience kit, SKU DYNJ0888159I. Convenience kits used for various procedures... Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 36 kits.
Why was this product recalled?
Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods
Which agency issued this recall?
This recall was issued by the FDA Devices on January 1, 2025. Severity: Moderate. Recall number: Z-0718-2025.