PlainRecalls
FDA Devices Moderate Class II Ongoing

MEDLINE LITHOTOMY, REF DYNJ50099C. Convenience kit used in medical/surgical procedures.

Reported: November 9, 2022 Initiated: September 30, 2022 #Z-0162-2023

Product Description

MEDLINE LITHOTOMY, REF DYNJ50099C. Convenience kit used in medical/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
96 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?
MEDLINE LITHOTOMY, REF DYNJ50099C. Convenience kit used in medical/surgical procedures.. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 96 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-0162-2023.