PlainRecalls
FDA Devices Moderate Class II Ongoing

BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.

Reported: November 9, 2022 Initiated: September 30, 2022 #Z-0160-2023

Product Description

BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.

Reason for Recall

Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.

Details

Units Affected
28 kits
Distribution
US Nationwide distribution in the states of CA, MN, NC, NY, OK, PA, TN, TX.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 28 kits.
Why was this product recalled?
Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 9, 2022. Severity: Moderate. Recall number: Z-0160-2023.