PlainRecalls
FDA Devices Moderate Class II Ongoing

Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F

Reported: August 28, 2024 Initiated: March 22, 2024 #Z-2710-2024

Product Description

Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F

Reason for Recall

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

Details

Units Affected
160 units
Distribution
Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 160 units.
Why was this product recalled?
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 28, 2024. Severity: Moderate. Recall number: Z-2710-2024.